tag:blogger.com,1999:blog-16483812214855278252024-03-13T04:22:27.139-07:00Papimi UKpapimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.comBlogger26125tag:blogger.com,1999:blog-1648381221485527825.post-66858991487679534772011-11-09T04:02:00.000-08:002011-11-09T04:05:34.785-08:00FREE ENERGY - By Prof. Dr. P.T. PAPPAS<div dir="ltr" style="text-align: left;" trbidi="on">
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<b><span style="font-size: x-large;">FREE ENERGY - THE GREATEST AND SIMPLEST PROOF OF MY LIFE</span></b></div>
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The result of the above TV tube (or Cathode Ray tube) is the final speed of an electron is bigger than its initial speed: U final > U<sub>X </sub>initial which can enter into another tube like this one; at point A, following the original direction of U<sub>X </sub>and similarly. into another such tube and so on... Finally redirected in to the first one at point A with the same direction as the original of U<sub>X</sub>, U reaching as much exponentially high values of free energy, towards infinity and self destruction, as with every other perpetual mobile happens, and without any relevant consumption of energy......<br />
This example proves the principle of creation with tremendous economic and social implications, when a limiter is applied to avoid infinity and self-destruction. .</div>
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<span style="color: red;"><b>IMPROVED VERSION <a href="http://papimi.gr/osc3.htm">click<sub>1</sub> here </a> for correcting the right end effect and <a href="http://papimi.gr/university.htm">click<sub>2 </sub>here</a> for answering several invited suggestions</b></span></div>
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<span lang="en-gb"><b>FIRST POSTED AND PUBLISHED WORLD WIDE BY THE AUTHOR ON 20/3/2010<br />P.T.P</b></span></div>
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<b><span lang="en-gb">NON CONSERVATION OF ENERGY-PRINCIPLE OF CONTINUOUS CREATION OF ENERGY- IN CONFORMITY OF THE GENERAL PRINCIPLE OF CONTINUOUS CREATION-see below (selection column) </span></b></div>
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<b><span lang="en-gb">USUALLY INCREASING - CREATING ENERGY </span></b></div>
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<b><span lang="en-gb">ENERGY PRODUCING SIMILAR ENERGY See relevant topics in the selection column</span></b></div>
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Standard TV Cathode or Oscilloscope tube with only one vertical diversion electrodes, electrostatically charged, assuming well insulated, without any leakage, provision is made for U<sub>x </sub>is big enough or most important, the distance between the electrodes of vertical diversion, so that no electrons reach the upper positive plate.</div>
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Assuming, though we doubt very much that the passing electron through the whole of the anode, has paid its energy ticket, the velocity U<sub>x </sub>at is determined as the accelerated velocity according to the potential difference between cathode and anode, without consuming any energy from the potential difference. We clearly claim that the vertical gained there velocity U<sub>Y is also totally unjustified. Below we prove this last statement.<br />The total kinetic energy of the passing electron through is therefore E = 1/2 mU</sub><sup>2</sup> = 1/2mU<sub>X</sub><sup>2 +1/2m U</sup><sub>Y</sub><sup>2 . .with </sup><sub>U</sub><sup>2=U</sup><sub>X</sub><sup>2 + U</sup><sub>Y</sub><sup>2 . and U .> U</sup><sub>X</sub></div>
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<sub>Which is the initial velocity after the electron passed the anode at point A and nothing is consumed there by this passing there.<br /> </sub></div>
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<sup>The energy 1/2m U</sup><sub>Y</sub><sup>2 </sup>is a created new energy- as free energy of the system This amount of energy can be repeated for as many electrons we can wait for,<b><br /><span style="color: red;"><span lang="el"> </span><a href="http://papimi.gr/osc2.htm">click here</a></span></b><span style="color: red;">,</span> for seeing the diagram of repeating gaining free energy electron<br />
and without any corresponding energy consumption. The principle of conservation of energy is not generally valid. Energy is not always conserved. See also PAPIMI as at least 120% over unity device, here. below (selection column). The above configuration is a miniature accelerator compared to CERN accelerator. However, what we are concerned is the relevant understanding of the people there about non conservation of energy or energy continuous creation or energy's possibility of increase to selfdistruction that these people did not expect.</div>
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<b><span style="font-size: medium;">The Principle of leas/t action for the above system for the Theoretical Phycist, CERN Scientist and any other relevant Professional</span></b>.</div>
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The principle of least action is considered as the most advanced method in Theoretical .Physics in this case. However, for conservation of energy, the symmetry with respect to time is required However, as we have already shown in an elementary way, there is no symmetry in time for the energy increases with time So one of the basic requirements of this Principle is not fulfilled in this case. Tautologically, therefore, the Principle of least action is trivial here and can not offer more than we have shown for the non conservation of energy of the above system.</div>
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If we are wrong, 100000 Euros reward for the first claimer, as it is offered in other places in this site. None has self made a claim today <span style="color: red; font-size: x-large;"><b><span lang="el">30</span>/<span lang="el">10/</span></b></span><b><span style="color: red; font-size: x-large;">2011</span><span style="font-size: large;"> </span></b>morning yet! <u><b><span style="font-size: medium;">We receive only supporting messages.</span></b></u></div>
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NEWER CONSIDERATION: THE ABOVE SUSPENSION IS CANCELLED 24 HOURS AFTER ITS ACTIVATION. NOTE:: THE SUSPENSION WAS FIRST IMPOSED TO ALLOW TIME FOR THE CORRECTNESS OF AN ARGUMENT, PRODUCED AN INVITED FELLOW PROFESSOR FROM A NORTHERN UNIVERSITY. THE ARGUMENT WAS FOUND INCORRECT</div>
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In case you have made a claim or to confirm your claim or because it was lost, please call personally Pro.PT Pappas at <span lang="el"> </span><span lang="en-gb">code </span>+30210. office number 9270807, Home number 9012028, Fax +302109011620 or mobile or cell phone, code + 30, number 6944338415, e-mail <a href="mailto:ppappas@papimi.gr">ppappas@papimi.gr</a>, local time +2 hours GMT (Greenwich Mean Time) or +3 hours GMT taking into account the silly summer time, in case, it is applicable..+ international code as defined by the calling country, 30 code for Greece, 210 code for the city of Athens. Ordinary postal address is not given for security reasons. <span style="color: red;"><b>VALID CONTACTS ARE THOSE GIVEN HERE BY PHONE ,FAX, AND E-MAIL.<br />SOME PEOPLE, NOT DARING TO CONTACT US PROPERLY. THEY ARE BLUFFING TO CREATE WRONG IMPRESSIONS BY HIDING FROM US THEIR ALLEGED OBJECTIONS. . </b></span><br />
<b><span style="color: blue;">LANGUAGE OF CONTACT SHOULD BE GREEK OR ENGLISH</span></b><br />
with the power of logic</div>
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Prof. Dr. P.T. PAPPAS</div>
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NOTE1: Claimers should contact us. See contacts in the front page. None has made a claim, today</div>
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NOTE 2: Claimers should make their claims on the current accepted physical laws taught at generally recognized Universities except the principle of conservation Energy which is shown here generally not correct..</div>
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NOTE 3 Do not hesitate to claim, nothing to lose, nothing to pay! All correspondence will be posted here. None has self made a claim oyet, morning</div>
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<b><span lang="el">30</span>/<span lang="el"><span style="color: red;">10</span></span></b><b><span style="color: red;">/2011<span style="font-size: large;">,</span> </span></b> neither by e-mail or directly by phone or Fax.<u><b><span style="font-size: medium;"> We receive only supporting messages</span></b></u>.</div>
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NEWER CONSIDERATION: THE ABOVE SUSPENSION IS CANCELLED 24 HOURS AFTER ITS ACTIVATION. NOTE:: THE <span lang="el">1</span>SUSPENSION WAS FIRST IMPOSED TO ALLOW TIME FOR THE CORRECTNESS OF AN ARGUMENT, PRODUCED AN INVITED FELLOW PROFESSOR FROM A NORTHERN UNIVERSITY. THE ARGUMENT WAS FOUND INCORRECT</div>
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A Second independent proof will be added here soon.......FOR THE PROOF SEE BELOW.</div>
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<span style="font-size: large;">Dedicated to the late Stefan Marinov and Leon Dragone who were dedicated in all their short lifes to perpetual mobile. I wish they were with us to know the above indisputable example.<br /><br />with the power of logic</span></div>
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<span style="font-size: large;">PTP</span></div>
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<b>Notice 0, The left or entering electron end effect is always accelerating, favoring our conclusions and results for the creation or excess energy.</b></div>
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<b> MATHEMATICAL PROOF BASED ON VARIATIONAL TECHNIQUES</b></div>
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The electric field of two opposite charges Ntice the corespondin end effects is relative very curved.</div>
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The electrical field of two elongated distributed opposite charges by a distance x, Notice the corresponding end effect is lessened with respect to the above end effects The radius of curvature of the end effects is shorterer the shorter is the radius of curvature compared the capacitor below. This a very important element here.</div>
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Similarly, the electric field of two elongated distributed charges, capacitor distributions. The length of distribution here is x +<span lang="el">Δ</span><span lang="en-gb">x. Notice the slight variation and inwards smoothening of the end effects lessened by a second and higher order but definite amount of magnitude. The longer is the capacitor </span><span lang="el">b</span><span lang="en-gb">y </span><span lang="el">Δ</span><span lang="en-gb">x the bigger is the radius of curvature at the end effects. Thi is a very key element here to prove, beyond any doubt, the non conservation of energy or better the creation of energy and from this creation of universe. See text.</span></div>
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Thus, checking the electrical lines in reality in a charged capacitor, the end effect of the capacitor is lessened the longer the capacitor is!</div>
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The end effect of the lines is obvious at the two ends of the capacitor. The higher position is the exit of the electron, the higher is the horizontal draw back on the electron. However, if we assume the capacitor becomes a little longer by an amount <span lang="el">Δ</span><span lang="en-gb">x The end effect of this lethening will be only secondary (second order or higher and of the opposite sign) to </span><span lang="el">Δ</span><span lang="en-gb">x .However the vertical gained velocity upwards of the electron will be inverse proportional to the first order of</span><span lang="el"> Δ</span><span lang="en-gb">x . This is a contradiction and excludes the fact the end effect of the electric field will compensates the extra energy gained by the electron. This proves that THE END EFFECT WILL NOT MAKE THE ENERGY TO BE CONSERVED AS IT ASSUMED IN CLASSICAL PHYSICS. Q.E.D</span></div>
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<span lang="en-gb">PTP</span><br />
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<span lang="en-gb">Source : </span><a href="http://papimi.gr/osc.htm">http://papimi.gr/osc.htm</a><br />
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<a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com</a></div>
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</div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-28186180154289763342011-11-07T03:46:00.000-08:002011-11-07T03:46:45.293-08:00THE PROOF OF FORCE LAW OF THE HIDDEN LAW OF AMPERE BY THE TRANSISTORS<div dir="ltr" style="text-align: left;" trbidi="on">
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IN THE OLDEST AND NEWER THEORY OF TRANSISTORS, THIS COMPONENT IS GIVEN WITH THE FOLLOWING DESCRIPTION AND WORKING DIAGRAM. TWO P CONTACTS ARE ATTACHED TO AN N PLATE MATERIAL. THE TWO CONTACTS ARE UNEQUAL THIS FACT IS NOT EXPLAINED IN BOOKS. APPARENTLY IT WAS FOND THAT THE PNP TRANSISTOR WAS WORKING MUCH BETTER LIKE THIS. SO THE EXPLANATION IS MISSING IN THE OLDER BOOKS UNTIL TODAY. THE WORKING PRINCIPLE OF THE TRANSISTOR IS ATTEMPTED TO BE EXPLAINED BY THE <u><b>PROCESS OF DIFFUSION.</b> </u>ELECTRONS PRESUMABLY, PASSING THE CATHODE MOTIVATED BY THE BASE<b><u>, </u>ARE DIFFUSED </b>TO THE COLLECTOR<b><u>. T O</u></b> THE COLLECTOR. THIS AN NAIVE CLAIM. IT DOES NOT EXPLAIN AT ALLWHY THE COLLECTOR IS NOT EQUIVALENT TO THE EMITTER AND WHY THE CONTACT OF A EMITTER TO THE BASE SHOULD BE SMALLER THAN THE CONTACT OF COLLECTOR TO THE SAME BASE.</div>
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THE EXPLANATION FOR THE SAID DIFFERENCE IN TERMS WITH THE AMPERE FORCE LAW IS AS FOLLOWS: THE CURRENT PASSING, THE CATHODE IS REPELLED ACCORDING TO THIS LOW ALONG TO THE FORWARD DIRECTION WHICH MAKES IT TO REACH THE COLLECTOR. THE VERY FACT THAT THE DENSER IS THIS CURRENT BY THE NARROWER CATHODE THE HIGHEST ARE THE REPELLING FORCES. THUS MAKING THE CONTACT OF THE ENTERING CURRENT BY NARROWING THE EMITTER, WE INCREASE THE PERFORMANCE OF THE TRANSISTOR, BY REACHING THE COLLECTOR EASIER. THOUGH BY MAKING THE OPPOSITE GEOMETRY WE DESTROY THE PERFORMANCE OF THIS TRANSISTOR. SO THE APPLICABILITY OF AMPERE LOW EXPLAINS THE DYNANICS AND THE CHOSEN GEOMETRY OF TRANSISTORS. THE FORCE LOW OF AMPERE IS EQUIVALENT TO THE LORENTZ LOW IN MANY CASES AND FOR THOSE CASES THE TWO LOWS ARE NOT EQUIVALENT, THE AMPERE LOW IS THE ONLY VALID.</div>
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IT REMAINS TO BE EXPLAINED WHY THIS LOW HAS DISAPPEARED FROM THE TAUGHT ELECTRODYNAMICS AND PHYSICS. ARE THERE SOME STRATEGIC AND UNKNOWN CONSEQUENCES OF THIS LOW?:. THE ANSWER OF THIS QUESTION IS <b>YES. HOWEVER. WE SHALL SEE THE HIDDEN CONSEQUENCE IN THE FUTURE....</b></div>
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CONTINUOUS....</div>
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Source: <a href="http://www.papimi.gr/transistors.htm">http://www.papimi.gr/transistors.htm</a></div>
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</div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-42045063667401103902011-11-07T03:40:00.000-08:002011-11-07T03:42:03.886-08:006TH, 7TH AND 8TH EXAMPLE OF ENERGY CREATION COMING FROM ELECTROMAGNETISM<div dir="ltr" style="text-align: left;" trbidi="on">
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<b><span style="font-size: x-large;">INTRODUCTION</span></b><br />
ALL 6,7 AND 8TH CONFIGURATION HAVE THE SAME CHARGED NEGATIVELY CATHODE. THE SAME GROUNDED ANODE WITH THE SAME HOLE TO ALLOW PASSAGE OF THE REPELLED ELECTRONS.<br />
CONFIGURATION 6 IS EQUIPPED WITH A NEGATIVELY AND ELECTROSTATICALLY CHARGED RING AS CLOSELY AS POSSIBLY TO THE ANODE AND ON THE RIGHT HAND SIDE.</div>
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THE ELECTRONS IN CONFIGURATION 6 AS SOON AS, THEY PASS THE HOLE OF THE ANODE , THEY ARE BEING REPELLED BY THE ELECTROSTATICALLY CHARGED RING, AWAY FROM IT. THUS INCREASING THEIR HORIZONTAL VELOCITY AND TOTAL ENERGY WITHOUT TO HAVE TO PAY ANY EXTRA POTENTIAL ENERGY TO HAVE TO CROSS THE HOLE.</div>
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CALCULATION OF GAINED FOR FREE ENERGY TO AVERY AWAY POINT, WHERE THE FIELD IS ZERO =<span style="font-size: medium;"><b> to the first approximation, ignoring induced charges on the anode (second order approximation)=<br />= E = Q/R<br />WHERE R IS THE RADIUS OF THE RING, AND Q IS THE TOTAL CHARGE ON THE RING.</b></span></div>
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CONFIGURATION 7 PRESUMABLY HAS A LITTLE CHARGED NEGATIVELY SPHERE ON THE RIGHT OF THE ANODE, REPRESENTING A NEGATIVE POINT CHARGE. THE POINT NEGATIVE CHARGE ACTS THE SAME WAY AS THE NEGATIVE RING OF CONFIGURATION 6, THUS INCREASING THE HORIZONTAL AND TOTAL ENERGY WITHOUT THE LOSS OF ANY CHARGE ON THE RIGHT OR ENERGY</div>
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<b><span style="font-size: large;">QUANTITATIVE CALCULATION OF INCREASED ENERGY.</span></b></div>
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<span style="font-size: medium;"><b>SUPPOSE THE POTENTIAL OF THE POINT CHARGE AT THE ENTRY POINT IS q/r<sub>1</sub></b></span></div>
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<span style="font-size: medium;"><b>WHERE q IS THE CHARGE ON THE SMALL SPHERE-POINT CHARGE AND r<sub>1</sub> IS THE DISTANCE OF POINT CHARGE TO THE HOLE.</b></span></div>
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<b><span style="font-size: medium;">THE POTENTIAL AT A FAR AWAY POINT IS</span>. </b><span style="font-size: medium;"><b>q/r<sub>2. </sub>THEN THE GAINED ENERGY IS:</b></span></div>
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<span style="font-size: medium;"><b>THE GAINED ENERGY PER PASSING ELECTRON AT A FAR AWAY POINT OF DISTANCE r<sub>2<br /> </sub>= to the first approximation, ignoring induced charges on the anode (second order approximation)=<br />E = (q/r<sub>1 </sub>- q/r<sub>2</sub>)xe </b></span></div>
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<span style="font-size: medium;"><b>WHERE e IS THE CHARGE OF THE PASSING ELECTRON.</b></span></div>
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CONFIGURATION 8 CONSISTS OF THE SAME ANODE AND CATHODE. ON THE RIGHT OF THE ANODE IT IS EQUIPPED WITH A NUTRAL ISOLATED PLATE. AS SOON THE ELECTRON PASSES OVER THE NUTRAL PLATE OPPOSITE ELECTROSTATIC CHARGES ARE INDUCED THERE, WHICH ATTRACT THE ELECTRON. THUS THE ELECTRON GAIN VERTICAL VELOCITY BY THIS ATTRACTION AS SMALL NEUTRAL PARTICLES ARE ATTRACTED BY A CHARGED BODY AS LONG AS THE ELECTRON COMES AWAY FROM THE PLATE THE ECTROSTATIC INDUCTION BECOMES WEAKER. THUS REDUCING THE HOLDING BACK VELOCITY.<br />
THUS THE GAINED OVER ALL VELOCITY AND ENERGY IS BIGGER.</div>
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<b><span style="font-size: x-large;">CONCLUSION</span></b></div>
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<span style="font-size: medium;"><b>WHAT IS CHARACTERISTIC IN THE 3 EXAMPLE CONSISTING OF THREE DIFFERENT OBJECTS:</b></span></div>
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<span style="font-size: medium;"><b>ONE CHARGED NEGATIVELY RING,</b></span></div>
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<span style="font-size: medium;"><b>ONE CHARGED NEGATIVELY SMALL BALL, POINT CHARGE,</b></span></div>
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<span style="font-size: medium;"><b>ONE CHARGED NEGATIVELY PLATE.</b></span></div>
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<span style="font-size: medium;"><b>IT IS THE NON SYMMETRY ON THE LEFT AND RIGHT HAND SIDE.</b></span></div>
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<span style="font-size: medium;"><b>ON THE LEFT THERE IS A GROUNDED ANODE WITH A SMALL HOLE, WHICH ANODE ACTS AS A FARADAY SHIELD FOR THE COMING ELECTRON. SO THE NEEDED APPROACHING SPENT ENERGY TO THESE OBJECTS IS MUCH LESS THAN THE DESCENDING GAINED ENERGY.</b></span><br />
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Cathode and anode are both grounded to zero potential. An electron with kinetic energy received by the heated cathode approaches the neutral anode. There on the anode, by induction, opposite positive charges, are accumulated, which attract and accelerate the electron. The electron passes the new hole again, which a negative concetretic negative ring is placed, as shown. The negative ring repells and farther accelerates the electron to the right towards the next anode. The whole process is repeated, increasing the velocity of the electron, farther and farther,..., making U<sub>0, </sub><U<sub>1., </sub>< U<sub>2,</sub>< U<sub>3</sub> .....</div>
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<span style="font-size: medium;"><b>Source: </b></span><a href="http://www.papimi.gr/678.htm">http://www.papimi.gr/678.htm</a></div>
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</div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-81884606778187161492011-11-07T03:37:00.000-08:002011-11-07T03:37:23.409-08:00IMPROVED EXAMPLE EASIER TO UNDERSTAND ENERGY CREATION<div dir="ltr" style="text-align: left;" trbidi="on">
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<a href="http://4.bp.blogspot.com/-MNXH-q1n1a4/TrfB430h_fI/AAAAAAAAAHY/pAgNlaHqKkg/s1600/cathode+ray+tube11.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="142" src="http://4.bp.blogspot.com/-MNXH-q1n1a4/TrfB430h_fI/AAAAAAAAAHY/pAgNlaHqKkg/s320/cathode+ray+tube11.jpg" width="320" /></a></div>
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This is an improved mode to understand energy creation or energy increase. All the positive potentials have been changed to zero. The plates of vertical displacement have move towards the anode as closely as possible. Then the passing electron is only repelled and is always accelerating. HOWEVER THE ELECTRON SPENT ENERGY UP TO THE ANODE, AFTER PASSING THE ONLY GAINS ENERGY FOR FREE AS THERE NO CONSUMPTION AFTER THIS POINT!!!!!!!!!!!!<br />IMPORTANT NOTICE: The anode is at zero potential as we said and it is very well known from electronics applications it acts also as an Faraday shield for the fields behind it.(For those who are mean I MIGHT MAKE THIS ANODE TO BE A COMPLETE CLOSED SURFACE BY CLOSING IT FROM THE LEFT END, MAKING IT A COMPLETE CLOSED FARADAY CAGE WITH A LITTLE HOLE ON THE RIGHT, ENCLOSING THE CATHODE . NOTHING WILL BE CHANGED !). Unless the little hole makes all the creation of energy !. Let me know by contacting me <a href="mailto:ppappas@papimi.com">ppappas@papimi.com</a> etc phones, and FAX.. I may publish your point unanimously with my answer together.<br />Notice also i<sub>1</sub> = 0, i<sub>2</sub> < i<sub>3 </sub>i<sub>3 </sub>-<sub> </sub>i<sub>2</sub> corresponds to the passing electrons. only. Typical value for this current 200 mA. It may go up to 2A or more. This current may charge or discharge the capacitor plates in less than 1 nanosecond. These values are given to show to an invited and objecting University professor, that a relative small energy system such as the horizontal capacitor's 1/2CV<sup>2 </sup> may divert the huge relative energy of the passing electrons VIt= 5000voltx2AXt</div>
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NUMERICAL EXAMPLE with typical (reasonable) values.<br />In the following we shall use only definitions and Mathematical <b><u>identities</u></b> that are always and under any circumstances <u><b>valid</b></u></div>
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Such as<br />Energy = mechanical work by definition = int(Fds)=int(m<sub>e</sub>du/dt)(ds)=int{m<sub>e</sub>udu}= 1/2m<sub>e</sub>u<sup>2</sup></div>
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Energy = electrical work by definition = eE, E = Electromotive Force (Voltage), using the better terminology of older Electrodynamics<br />(KOSTA) Remember that q on a conductive surface or a conductor is a function -distribution, not a constant. Also that, the E.M.F. on a conductor or a surface is zero, so no matter whatever the charge distribution is on it, the conductor or the metallic surface remains always equi-potential that determines the electric field outside and near it!<br /><br />therefore eV = 1/2m<sub>e</sub>v<sup>2 </sup> therefore<br /><br />v = (2eV/m<sub>e</sub>)<sup><span style="font-size: xx-small;">1/2 </span></sup>= (2x 5x10<sup>3</sup>x1,602 X 10<sup>-12 </sup>10<sup>-8</sup>Joules / 9,109 x 10<sup>-28 </sup>x 10<sup>-3 </sup>Kgr)<sup>1/2</sup> = (1,7587x10<sup>14</sup>)<sup>1/2</sup> = 1,326X10<sup>7</sup> meters/ seconds in non relativistic mechanics. So for relativistic mechanics, the passing velocity is close to the velocity of light. Approximately: v= 98% C VELOCITY OF LIGHT</div>
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mass to electron charge m<sub>e</sub>/ e = 1/(5.2727x 10<sup>17 </sup>ESU x gr<sup>-1</sup>)<br /> 5000eV =5000eE = 5x10<sup>3</sup>x1,602 X 10<sup>-12 </sup>erg= 5x10<sup>3</sup>x1,602 X 10<sup>-12 </sup>10<sup>-8</sup>Joules</div>
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m<sub>e</sub> =9,109 x 10<sup>-28 </sup>g r= 9,e109 x 10<sup>-28 </sup>x 10<sup>-3 </sup>Kgr<br /><br />distance cathode to the anode = irrelevant however with higher order corrections due to the small hole, which tends to zero, the bigger this distance, we choose.</div>
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Homogeneous Intensity of field between the plates of big capacitor = V/L= -200Volts/1cm=-20000Volts/ meter</div>
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L = 1 cm separation = 0,01meters</div>
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V = -200 VOLT</div>
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E = Electromotive force of the cathode = -5000 Volts</div>
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Length of the capacitor S= 300 cm= 3 meters</div>
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Width of the capacitor = 40 cm= 0,4 meter</div>
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time travel between the plates = t=S /v= 3 Meters/30000000 m/sec =3/3x10<sup>-8</sup>seconds = approximately 10 nanoseconds.</div>
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t time passing through the capacitor = approximately 10 nanoseconds<br /> </div>
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The passing short time is short and it will correspond to a practical small increase in the vertical velocity and due, to the electron's high rapidness of descending from the capacitor with a great velocity, the electron results also to a practical small increase in the horizontal velocity. Therefore for this realistic and reasonable example we have a small but definite increase in the over all velocity and energy.<br />Therefore this definite but in practice small increase of velocity and corresponding energy explains why experimentally energy was not known to increase.</div>
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Improving factors for making the energy increase bigger are to minimize the cathode| to the anode potential difference down to less even than 50 Volts, even down to -15volts (cut off negative anode potential), letting even thermal electronss through, to increase the capacitor length to 30 meters or more, to increase the potential of the capacitor plate to even 5000 or more and finally to decrease the diameter of the hole which what ever small it will be, still (thermal) electrons will go through it even without any cathode to anode potential,. Q.E.D.</div>
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Matters like the self degreasing system's entropy will be published on another occasion elsewhere</div>
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Source : <a href="http://www.papimi.gr/IMPROVED.htm" id="internal-source-marker_0.92294732760638" style="text-align: left;"><span style="background-color: transparent; color: #000099; font-family: Arial; font-size: 10pt; font-weight: bold; vertical-align: baseline; white-space: pre-wrap;">http://www.papimi.gr/IMPROVED.htm</span></a><span style="background-color: transparent; font-family: Arial; font-size: 10pt; font-weight: bold; text-align: left; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;"> </span></div>
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</div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-10604580662234120082011-10-27T00:15:00.000-07:002011-10-27T00:15:08.768-07:00<div dir="ltr" style="text-align: left;" trbidi="on">
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<span style="color: #4a4a00; font-family: Arial; font-size: x-large;"><b>5
CASE HISTORIES OF</b></span></div>
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<b><span style="color: maroon; font-family: Arial; font-size: x-large;">LAST STAGE AIDS PATIENTS</span><span style="color: maroon; font-family: Arial;"><br />
</span><span style="color: #004000; font-size: x-small;">TREATED by<br />
Nick Tsilimigakis, MD<br />
</span></b></div>
<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="_Toc402066478"></a><span style="color: #930000;"> </span><span style="color: #930000; font-size: medium;"><b>1. S.T. Female 30 years of age.</b></span><span style="color: #930000;"> </span><br />
<br />
A. Therapy Method: <br />
a. Use of Device for determining patients Bioenergy Condition; <br />
b. Use of Micro-currents Device; <br />
c. Use of <b>PAP IMI</b> Device since August 1994. At the beginning of treatment
(November 1992) the patient was additionally receiving AZT. <br />
<br />
B. Clinical picture before therapy beginning: Significant loss of energy,
Lymphadenitis, Hodgkin, Emaciation, Weight down to 46 Kgr. <br />
<br />
C. Laboratory findings before therapy beginning: Anemia, Leukopenia, CD4 29. <br />
<br />
D. Patient Development during therapy: <br />
a. During the first month of therapy significant improvement of physical condition,
Anemia improvement, Restitution of the white cell count to normal level, weight increase
by 3 Kgr, improvement of Bioenergy indexes. <br />
b. During the end of the second month: Excellent physical condition, Normal counts for
red and white blood cells, weight increase by 4Kgr, Indexes of Bioenergy Condition to
normal. <br />
c. At the end of six month therapy: Excellent physical condition, full vocational
activities, complete reduction of lymph nodes swelling, weight recovery to level before
illness: 56 Kgr, CD4 90 <br />
d. End of the first year Treatment: Clinical picture to excellent picture, CD4 count
120. <br />
e. End of the second year Treatment: as above, CD4 count 165. <br />
f. During the third year: The <b>PAP IMI</b> is applied around thymus. At the end of
the third year CD4 clime to 350 count. During this year, no other medication was taken
against HIV. Physical condition top excellent. <br />
<br />
<br />
<br />
<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="_Toc402066479"></a><span style="color: #930000;"> </span><span style="color: #930000; font-size: medium;"><b>2. K.H. Male 60 years of age.</b></span><br />
<br />
A. Method of treatment: <br />
a. Use of Diagnostic Device for Bioenergy Condition of Body; <br />
b. Use of Microcurrent Device, <br />
c. Use of <b>PAP IMI</b> Device, d. Intaking of big doses of Vitamin C; <br />
d. Intake of mineral traces. <br />
<br />
B. Clinical picture before treatment: Significant loss of Energy, Emaciation continuous
fervescence 40-42 for two months with no response to continuous antibiotic Intaking,
pneumonia carini, diarrheal syndrome. <br />
<br />
C. Laboratory findings before treatment: Anemia, Leukopenia, CD4 count 10. <br />
<br />
D. Patient Development during the treatment application: <br />
a. With the application of <b>Tsilimigakis </b>therapy and with the antibiotics being
all discontinuous, during the first 10 days temperature dropped to 37-37.5 degrees C. <br />
b. During the end of the second month of treatment patient shows complete restitution
to his Bioenergy body condition. Patients physical condition becomes excellent,
significant improvement to the laboratory indices. Patient returns to work. CD4 24.
Complete cure from pneumonia. Weight increase by 4 Kgr. <br />
c. During the end of the first semester: Excellent physical condition. Lu<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="BM_1_"></a>ng X ray examination normal, weight recovery to normal from 60 Kgr
(before), to 76 Kgr (after). During all the time of the therapy no known medication
against HIV was taken by the patient. <br />
<br />
<br />
<br />
<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="_Toc402066480"></a><span style="color: #930000;"> </span><span style="color: #930000; font-size: medium;"><b>3. B.D. Male 47 years of age.</b></span><br />
<br />
A. Method of treatment: <br />
a. Use of Diagnostic Devices for the Bioenergy Condition of the Body. <br />
b. Use of Microcurrent Device, <br />
c. Use of <b>PAP IMI</b> <br />
d. Intake of Vitamin C, Mineral Traces, multivitamins, iron. <br />
<br />
B. Clinical Picture before the treatment: Significant loss of Energy, significant
Emaciation, continuous diarrheal syndrome, excessive anemia. <br />
<br />
C. Laboratory findings before treatment: Anemia, Ht 22, Leukopenia, CD4 count 30. <br />
<br />
D. Patient development during the application of treatment: <br />
The application of <b>Dr Tsilimigakis</b> treatment had resulted the significant
improvement of patients physical condition during the fist month. weight increased by 4
Kgr. There was significant improvement of the laboratory findings. The Bioenergy body
condition got to normal level for healthy persons. Diarrhea was discontinuous. patient
returned to his work. By the end of the first semester patient had excellent physical
condition, got normal body weight, CD4 count to 80. Patient was not taking any medication
against HIV. <br />
<br />
<br />
<br />
<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="_Toc402066481"></a><span style="color: #930000;"> </span><span style="color: #930000; font-size: medium;"><b>4. B.A. Male 30 years of age.</b></span><br />
<br />
A. Method of treatment: <br />
a. Use of Diagnostic Devices for Bioenergy Condition of Body; <br />
b. Use of Microcurrent Device, <br />
c. Use of <b>PAP IMI</b> Device, d. Intaking of big doses of Vitamin C; <br />
e. Intake of vitamins and mineral traces. <br />
<br />
B. Clinical picture before treatment: Significant loss of Energy, Emaciation continuous
fervescence 38-39 C, diarrheal syndrome, weight 56 Kgr. <br />
<br />
C. Laboratory findings before treatment: Anemia, significant reduction of plateless
(28,000), Cd4 count to 70, significant loss of white cells. <br />
<br />
D. Patient development during the application of treatment: <br />
a. During the first two weeks, the patient shows improvement of his physical condition,
weight increased by 2 Kgr, reduction to the frequency of diarrhea. <br />
b. By the end of the first month of therapy patient shows sufficient good physical
condition, weight increased by 3 Kgr (total increase in the fist month 5 Kgr). Diarrhea
stopped completely. laboratory verified improvement of anemia, Ht 31, restitution of white
cells to normal healthy level. Plateless increase to 48,000. Patient got out of Hospital
to receive the <b>Tsilimigakis </b>treatment and was receiving combinations of AZT, DDI,
3TC. <br />
<br />
<br />
<br />
<a href="http://www.blogger.com/blogger.g?blogID=1648381221485527825" name="_Toc402066482"></a><span style="color: #930000;"> </span><span style="color: #930000; font-size: medium;"><b>5. M.K male. 30 years of age.</b></span><br />
<br />
A. Method of treatment: <br />
a. Use of Diagnostic Devices for Bioenergy Condition of Body; <br />
b. Use of Microcurrent Device, <br />
c. Use of <b>PAP IMI</b> Device, <br />
d. Intaking of big doses of Vitamin C; <br />
e. Intake of mineral traces. <br />
<br />
B. Clinical picture before treatment: Significant loss of Energy, Excessive
lymphadenitis of cervical lymph nodes due to non Hodgkin lymphoma. <br />
<br />
C. Laboratory findings before treatment: Anemia, Reduction of White cells, CD4 count
300.<br />
<br />
D. Patient Development during the treatment application: <br />
a. By the end of two weeks, the patient shows improvement of his physical condition,
reduction of the swelling of cervical lymph nodes. <br />
b By the end of the first month: Excellent physical condition, farther reduction of
swollen cervical lymph nodes. Laboratory examinations for red and white cells normal. The
patient was taking AZT, DDI and had been through chemotherapy process without patient's
organism positive response. <br />
<br />
<br />
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<span style="color: maroon; font-size: large;"><b>Notice for optimizing the method</b></span></div>
A. Patients usually after a two month treatment, because: <br />
1. they are encouraged by the significant improvement of their physical condition; and <br />
2. because of financial difficulty to self cover the treatments (not yet covered by
health insurance policies), do not follow recommendation and drop the number of treatments
they receive. <br />
B. Similarly, there is a problem of follow up and retrieving laboratory examinations
taken in major hospitals the AIDS patients initial report and receive treatments. Major
Hospitals are unwilling to corporate in carrying recommended by us examinations, as well
as in providing existing results. <br />
<b>I suggest two solutions to this problem.</b><br />
The first is a short time solution by supplementing patients expenses, for their
therapy and required examinations.<br />
The second solution is the set up of a specialized center in the form of a clinic or
Hospital for the correct self application of the method.<br />
Presently, the application of the method incurs a lot of problems and difficulties, and
results in abstaining from optimum efficacy, which otherwise could have been achieved.<br />
B. For patient follow up treated for AIDS and other major diseases, the patients body
Bioenergy condition is very significant. During, many years of experience and research
stages, it has been understood what daily is realized in curative medicine, i.e., many
times patients with more serious adverse prognosis carry a more successful follow up with
respect to others with less serious adverse prognosis. A decisive factor is the patients
General Bioenergy Body condition, which does not show in the partial laboratory findings
and prognosis. <br />
If we call with A the patient state defined by all the laboratory and clinical
findings; and B the state of Bioenergy condition of the patient, not included in the
previous laboratory and clinical description of the patient, then patient's true Condition
is the resultant of both states A and B, given by their product AxB.<br />
This is confirmed in the above cases which show that the patient's General Condition
right after Bioenergy treatments is much higher and too optimistic than the condition
expected by the laboratory findings alone.<br />
In the present situation, it is considered very important the diagnosis of Patients
Bioenergy Condition for setting the plan for his therapy.<br />
C. Applications of the present therapeutic method, other than the applications to
various types of cancer and AIDS with impressive and increasing number of successes,
appear to give similar results and achievements in: <br />
Rheumatoid Diseases, <br />
Asthma, <br />
Intestinal and Stomach Ulcers, <br />
Burning and various Edemas, <br />
Fractures with impressive healing speed, <br />
Eye problems and conditions, <br />
Brain Damages, <br />
Dermatopathy and Skin Diseases, <br />
Various Inflammatory Diseases, <br />
Cosmetology, <br />
The method may provide also significant results in prognosis and preventing decreases
as well as in retarding the process of aging of body cells. <br />
<b>Nick Tsilimigakis, MD</b>, December 12, 1995.<br />
<br />
Source: <a href="http://papimi.gr/aidssum.htm">http://papimi.gr/aidssum.htm</a><br />
<br />
<a href="http://papimiuk.blogspot.com%20/">http://papimiuk.blogspot.com </a><br />
<br />
<br />
<br /></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-7992568594819096512011-10-26T05:41:00.000-07:002011-10-26T06:23:41.634-07:00Magnetic Resonance Images for Brain Damage and Skull Osteonecrosis Recovery<div dir="ltr" style="text-align: left;" trbidi="on">
<span style="color: maroon;"><b>Report by patient herself.</b> </span><br />
Patients S.S., female, 46 years old, (1997) explains in a letter written by herself to
us that the <b>PAP IMI</b> device actually healed her brain damages, though before
treatments she was unable to write, talk and walk properly. She provided to us MRIs before
and after to prove her brain atrophy healed, which we exhibit below for comparison.<br />
<br />
S.S. was suffering from <b><u>skull osteonecrosis</u></b> and <b><u>brain damage.</u></b>
According to her, at the age of 12, the first amalgam placements caused her severe memory
loss, behavioral problems, severe lethargy, "lead gut" (constipation) facial
pallor (mercury glow) and cold hands. By the age 20, S.S. was being treated with hormone
therapy for low thyroid, lack of menstruation (pituitary problem) and of bile salts
(constipation) without any clue yet that <b>mercury</b> (Hg) was the culprit. S.S. made
high-test scores in the college, but she forgot completely everything she studied in a
matter of weeks after every exam. She was frightened for her situation and dropped her
studies in the third year !<br />
<br />
S.S. found herself being 45 years old, on Social Security Disability, with no cure for
the near future, as she says, until she came to the PAP IMI treatments.<br />
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Source: <a href="http://papimi.gr/brain.htm">http://papimi.gr/brain.htm</a><br />
<a href="http://www.blogger.com/goog_1891434186"><br />
</a><br />
<a href="http://papimiuk.blogspot.com/"> http://papimiuk.blogspot.com</a></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-39505403127043229262011-10-26T00:52:00.000-07:002011-10-26T00:57:33.884-07:00<div dir="ltr" style="text-align: left;" trbidi="on">
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<b><span style="color: maroon; font-size: x-large;">TREATING HORSES WITH PAPIMI</span><span style="color: maroon;"><br />
</span><span style="color: #004000;">SUMMER 1995<br />
</span><span style="color: #693434;">TESTS OF PAP IMI ON HORSES AT THE ATHENS RACE TRACK<br />
</span><span style="color: #400000;">BY MARK KARATZAS.<br />
</span><span style="color: #693434;">SUMMARIES OF THE MOST SIGNIFICANT CASES</span></b></div>
<div align="center">
<br /></div>
<ol>
<li>A horse with broken tenon which considered unable to run and useless for races for ever,
after two days treatments start exercising and in one week was raceable with normal
mobility.</li>
<li>Horse with wounds on the knees by being kicked by another horse and excluded from races
for six weeks after being treated was able to race the next day.</li>
<li>Horse with marks and wounds on the skin from unknown dermatopathy cleared in two days in
most parts. The bigger main wound was cleared by 80%. Unbelievable and spectacular
recovery of unknown dermatopathy.</li>
<li>Horse with postoperative wounds that normally would close in a month, after being
treated three times completely healed in three days.</li>
<li>Horse with spine problem unable to carry a race, after being treated twice 30 minutes
locally on the back, recovered completely.</li>
<li>Numerous other horses with various specified and unspecified conditions, broken tenons,
leg problems recovered with the spectacular and unexpected short time.</li>
</ol>
<br />
<br />
<div align="center">
<b><span style="color: maroon; font-size: medium;">TRANSCRIPT BY Dr. P. L</span><span style="color: maroon;"><span style="font-size: medium;">.</span><br />
</span><span style="color: #3c3c00; font-size: large;">Treatment of Race Horses with the PAPIMI<br />
at Aqua Caliente Race track</span></b></div>
In the summer of 1995 a horse trainer together with a medical doctor used the <b>PAPIMI</b> to treat about 10 race horses in their stalls at the Aqua Caliente race track near
Tijuana, Mexico. These were among 500 horses some of which were being trained for the 1996
Olympics. Treatments were given over about a one week period. <br />
They used it to successfully treat the ankles of the horses right in the hots where
they get splints. <br />
They also had good results in treating rheumatoid areas which were known to be
problematic from long time experience. Also they used it to treat saddle soars which had
caused big fistulas. <br />
These were found to heal quicker as a result of the <b>PAPIMI</b> treatments without
any noticeable adverse effects. The animal was able to tolerate the sound of the machine's
operation without too much problem. <br />
They also successfully treated some horses for piroplasmosis, a protozoan parasite of
the blood vessels. Three modalities were used: nosodes (homeopathic remedies), the <b>PAPIMI</b>, and ultraviolet treatment of the blood<br />
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<h1 id="watch-headline-title" style="padding-bottom: 8px;">
<span class="" dir="ltr" id="eow-title" style="vertical-align: top;" title="PAPIMI treatment for horse">PAPIMI treatment for horses</span></h1>
<h1 id="watch-headline-title" style="padding-bottom: 8px;">
<span class="" dir="ltr" id="eow-title" style="vertical-align: top;" title="PAPIMI treatment for horse"><span style="font-size: small;">http://papimiuk.blogspot.com</span> </span></h1>
<h1 id="watch-headline-title" style="padding-bottom: 8px;">
<span class="" dir="ltr" id="eow-title" style="vertical-align: top;" title="PAPIMI treatment for horse"> </span></h1>
<h1 id="watch-headline-title" style="padding-bottom: 8px;">
<span class="" dir="ltr" id="eow-title" style="vertical-align: top;" title="PAPIMI treatment for horse">
</span></h1>
<br /></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-18880088369069382232011-10-24T04:14:00.000-07:002011-10-26T00:54:16.081-07:00PEMF History<div dir="ltr" style="text-align: left;" trbidi="on">
<iframe allowfullscreen="" frameborder="0" height="344" src="http://www.youtube.com/embed/SYgz-JneXoY?fs=1" width="459"></iframe></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com1tag:blogger.com,1999:blog-1648381221485527825.post-27338141071433180902011-10-17T05:01:00.000-07:002011-10-17T05:01:51.008-07:00Why Few People Seldom Get Heart Cancer<div dir="ltr" style="text-align: left;" trbidi="on">
<div class="title">
<h2>
Why Few People Seldom Get Heart Cancer</h2>
</div>
BY DR. GARRY F. GORDON, MD, DO, MD(H)<br />
<br />
Considering all of the areas a person can get cancer, it makes you
wonder why heart cancer is so rare. One interesting theory is that the
heart is the most electrical organ in the human body. Heart cells have a
voltage of 120 megavolts (mV) and, in some cases, a slightly higher
voltage. This is almost twice the voltage of some other cells in the
body.<br />
<br />
Pulsed Electromagnetic Frequency (PEMF) acts as a “whole-body battery
charger” by recharging each of the 70 trillion cells in your body.
Though it’s impossible to charge your cells as high as the heart, we can
raise the voltage of the cells in your body up 70 mV, or to 110 mV in
the case of high-activity athletes. In most people, you can expect
between 70 mV and 90 mV.<span id="more-1440"></span><br />
<img alt="" class="alignright size-full wp-image-1441" height="300" src="http://www.greenlivingaz.com/wp-content/uploads/heart-web.jpg" title="heart-web" width="300" />PEMF
acts like a spark, ignition, or impulse that keeps the cells charged at
an ideal voltage. Just like a car, the human body needs fuel, oxygen
and ignition – a spark plug. All metabolic processes are driven by this
cellular charge: adenosine triphosphate (ATP) production, oxygen,
nutrient absorption, waste removal, immune function and reproduction.<br />
<br />
When your cells are sick, they lose energy. As a result, there is
not enough ATP and your cells’ voltage drops to 40-50 mV. People that
are sick potentially have voltages as low as 20 mV (in the case of
cancer). Cancer cells typically have a voltage of 20 mV and are in
fermentation, meaning they need 10 times more energy from the
environment.<br />
<br />
PEMF builds energy within your cells, oxygenating and alkalizing the
cells. PEMF improves circulation so the conversion of nutrients and
oxygen inside the body can occur at optimum performance. PEMF also
increases the efficiency with which your body processes and expels waste
matter and keeps your system running smoothly.<br />
<br />
With physics being used for mainstream medicine, electricity has been
used to treat glioblastoma. I prefer PEMF, but this news is the
beginning of a new understanding in medicine about physics, which I
predict will lead to many exciting things like NeuroStar TMS Therapy®.
This NeuroStar system is FDA-approved and in use today at UCLA, Stanford
and Yale, but so far only approved for unresponsive depression.<br />
<br />
Many of those involved are probably unaware that PEMF devices are
similar to the <a href="http://papimiuk.blogspot.com/">PAPIMI® NanoPulse Therapy</a> device used in Greece to treat
cancer. The FDA has approved the new NovoTTF (for tumor treating
fields), that uses an electrical field to disrupt the division of cancer
cells in the brain, and is being developed for use in patients with
glioblastoma, although only after standard treatments fail. Even so,
this is a major breakthrough! PEMF generates microelectric currents and
magnetic fields, so it will do more than this newly approved treatment.<br />
<br />
There is also another logical explanation for why PEMF is doing so
much good for people. This involves an electric charge like the newly
approved FDA device for brain cancer and turns on the body’s healing
power. Now combine that with my FIGHT program, and be prepared for
miraculous healing!<br />
<br />
Source: <a href="http://www.greenlivingaz.com/?p=1440">http://www.greenlivingaz.com/?p=1440 </a><br />
<a href="http://www.blogger.com/goog_538206809"><br /></a><br />
<a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com</a></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-17861392363099125492011-10-17T04:50:00.000-07:002011-10-27T00:14:50.338-07:00<div dir="ltr" style="text-align: left;" trbidi="on">
<b><span style="font-size: large;">Nanopulses tweak the innards of cells</span></b><br />
<br />
<span style="font-size: small;">A method that would allow doctors to tweak the innards
of cells without even touching a patient's body is being developed in
the US and Greece..<br />
<br />
The technique is still in its infancy, and it is still not clear
exactly what it does to cells. But initial experiments suggest it might
one day be possible to use the technique to treat cancer, speed up
healing or even tackle obesity.<br />
<br />
The method involves exposing cells to an extremely powerful electric
field for very brief periods. "The effects of these pulses are fairly
dramatic," says Tom Vernier of the University of Southern California in
Los Angeles, who will present some of his team's results at a
nanotechnology conference in Boston in March. "We see it as reaching
into the cell and manipulating intracellular structures."<br />
<br />
Applying electric pulses to cells is not new. In a technique called
electroporation, electric fields that last hundreds of microseconds are
applied to cells. The voltage charges the lipid molecules in the cell
membrane, creating transient holes in the membrane. The method can be
used to help get drugs or genes into cells.<br />
<b></b><br />
<b>Major physiological event</b> <br />
<br />
But the latest technique involves more powerful electric fields, with
gradients of tens of megavolts per metre, applied for much shorter
periods. These nanosecond-pulsed electric fields are too brief to
generate an electric charge across the outer membrane of cells, but they
do affect structures within cells.<br />
<br />
One of the main effects seems to be calcium release from a cellular
structure called the endoplasmic reticulum. "In a nanosecond, we cause
this major physiological event in the cell," says Vernier. "It's
completely indirect and remote, and it's an extremely rapid transition."
<br />
<br />
The nanopulses can also trigger cell suicide. Teams led by Vernier,
Karl Schoenbach of Old Dominion University and Stephen Beebe of Eastern
Virginia Medical School, both in Norfolk, Virginia, have shown that
nanopulsing can kill tumour cells in culture.<br />
<br />
The pulses do not just fry cells, but lead to changes such as the
activation of enzymes called caspases, an early step in cell suicide.
How the pulses do this is not clear, but Vernier says the effect is not
related to calcium release. <br />
<b></b><br />
<b>Cell suicide</b> <br />
<br />
So could nanopulsing help treat cancer? In a preliminary test,
Schoenbach and Beebe used needle-like electrodes to generate pulses near
tumours in mice. Nanopulsing slowed the growth of tumours in four mice
by 60 per cent compared with tumour growth in five untreated mice. The
researchers hope that with better delivery systems they could make the
tumours shrink.<br />
<br />
Beebe's team has also found that the pulses can trigger suicide in
the cells that give rise to fat cells, possibly opening up a new way of
treating obesity, Beebe speculates. <br />
<br />
And Vernier is working with doctors at the Cedars-Sinai Medical
Center in Los Angeles to see if nanopulses can speed up the healing of
wounds. "We do see an effect, but that's about all I can say now," he
says.<br />
<br />
The next step is to develop a way to deliver the pulses to cells and
organs deep within the body. Theoretical models suggest that nanosecond
pulses of broadband radio signals could do it. "An array of such
antennas would create, through superposition of electric fields, a very
high electric field right where we need it," says Schoenbach.<br />
</span><span style="font-size: small;"><br /></span><br />
<span style="font-size: small;">Source: </span><br />
<span style="font-size: small;">Anil Ananthaswamy, 06 February 04, <i><b>New Scientist</b></i> <a href="http://www.newscientist.com/news/news.jsp?id=ns99994635">http://www.newscientist.com/news/news.jsp?id=ns99994635</a></span><br />
<span style="font-size: small;"><br /></span><br />
<span style="font-size: small;">http://papimiuk.blogspot.com </span><br />
<span style="font-size: x-small;">
</span></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-83995315407496088982011-10-14T04:01:00.000-07:002011-10-14T04:22:48.396-07:00Electrical Nanopulses Might Kill Tumors<div dir="ltr" style="text-align: left;" trbidi="on">
<div class="itemTitle">
<h3>
<span style="font-size: small; font-weight: normal;">Killing cells affected by cancer while leaving healthy ones alone is not a new idea. But, in "<a href="http://www.nature.com/nsu/040315/040315-2.html">Ultra-fast shocks scramble cells</a>,"
Nature describes a new approach based on electrical nanopulses. These
electric shocks last only a few billionths of a second while reaching
during this very short amount of time power levels of terawatts. They
also are very intriguing, apparently forcing cancer cells to commit
suicide.</span> </h3>
<h3 style="font-weight: normal;">
<span style="font-size: small;">The technique involves blasting cells with nanopulses. These
are high-power electrical bolts that last a few billionths of a second.
They deliver millions of volts - enough power to light up a city, but
each burst lasts much less than the blink of an eye.</span> </h3>
<h3 style="font-weight: normal;">
<span style="font-size: small;">Longer shocks blow a cell apart, but researchers have found
that the fleeting nanopulses leave the cell membrane unaffected while
mixing up its insides. Now they are working out how to vary the timing
and intensity of the shocks to make cells behave in specific ways.</span></h3>
</div>
Here are two images showing how ultrashort pulses affect the
intracellular structure, leaving the cell membrane intact (Credit:
Center for Bioelectrics).<br />
<table border="0" style="width: 520px;">
<tbody>
<tr>
<td width="180"><img alt="Cell touched by a nanoplulse" border="0" height="230" src="http://radio.weblogs.com/0105910/images/nanopulse1.jpg" width="160" /></td>
<td width="340"><img alt="Effect of a nanopilse on a cell" border="0" height="230" src="http://radio.weblogs.com/0105910/images/nanopulse2.jpg" width="320" /></td></tr>
</tbody></table>
Is this technique ready for human deployment? Not quite yet.<br />
<blockquote>
There is plenty to be worked out before the human body is
zapped with nanopulses. James Weaver, who studies electrical effects in
cells at the Massachusetts Institute of Technology, Boston, says they
are at an early stage: "There are maybe ten papers published showing
that something dramatic is happening."</blockquote>
One puzzling aspect of this technique is the electric shocks are pushing cells to commit suicide. Scientists are not sure why.<br />
<blockquote>
One of the most significant discoveries was that nanopulses
make mammalian cells commit suicide, rather than blowing them up. This
is a relatively gentle way of killing, because scavenger cells come and
swallow the debris. By contrast, long electric shocks explode cells and
liberate toxic molecules that cause inflammation and pain.</blockquote>
<blockquote>
For this reason, researchers hope to use nanopulses to kill
cancer cells while leaving healthy tissue intact. Karl Schoenbach's team
at the <a href="http://www.odu.edu/engr/bioelectrics/"><b>Center for Bioelectrics</b></a>
in Norfolk, Virginia, has already shown that the pulses can shrink
mouse tumours by over 50%, and is working on catheters or non-invasive
ways to deliver the shocks to the body.</blockquote>
For more information about their research projects, you can look at <a href="http://www.odu.edu/engr/bioelectrics/html/research.html"><b>this page</b></a> or check <a href="http://www.odu.edu/engr/bioelectrics/Website.pdf"><b>this presentation</b></a> (PDF format, 19 pages, 1.31 MB).<br />
<i>Source: Helen Pearson, Nature, March 16, 2004</i></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-21876998267625586222011-10-12T05:08:00.000-07:002011-10-12T05:10:22.827-07:00<div dir="ltr" style="text-align: left;" trbidi="on">
<div style="text-align: justify;">
<b><span class="">The PAP IMI operating principle and mechanism of action</span></b></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
The PAPIMI device produces pulsed electromagnetic type ELF
(Extremely Low Frequency), also known as waves PEMF (Pulsed Electro
Magnetic Field). These waves, given their very short
duration (40-50 microseconds) do not heat the tissue and are able to
cross biological tissue up to 15 to 20 inches deep, thus favoring the
stimulation and regeneration because they act directly on the physiology
the cell.</div>
<div style="text-align: justify;">
</div>
<div style="text-align: justify;">
The pulse is produced in a Plasma ROOM, located inside a solenoidal probe in concentric coils. <span class="">The probe consists of a silicone tube containing air is circulated in which an electric current that turns the air into plasma. </span>The
way that gets the electromagnetic pulse makes it 100% biocompatible,
because it is rich of typical frequencies of the constituent elements of
air and the necessities of life, such as oxygen and nitrogen.</div>
<div style="text-align: justify;">
</div>
<div class="jce_caption" style="display: inline-block; float: left; margin: 6px; width: 322px;">
<img alt="Figure-1" height="295" src="http://www.biot.it/site/images/stories/prodotti/papimi/figura-1.jpg" style="float: left;" width="322" />
<br />
<div class="jce_caption" style="text-align: left;">
<span style="color: maroon;">Figure 1</span> Membrane potential</div>
</div>
<div style="text-align: justify;">
The PAPIMI device is used to reactivate the cell physiology in all
pathologies osteo-articular muscle and nerve, and also eliminates the
pain.</div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<span class="">The pain is usually
caused by trauma, injuries and accidents of various kinds that
determine tissue degeneration, inflammation and, therefore, pain. </span>The
multiplicity of agents damaging the body responds with a unique defense
mechanism, inflammation, and repair the injured tissue activates
mechanisms more or less specific. At the cellular level,
the inflammatory state leads to a lowering of the membrane potential
which, in turn, causes a reduction of the normal activity of the cell
involved, and a reduction of its metabolism.</div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
Reduces the normal transfer
of nutrients from outside, through the specific mechanisms of exchange,
which, first of all, the sodium potassium pump, and reduces the
elimination of waste substances toxic to the cell. Gradually,
the cell becomes depleted of oxygen, is enriched with toxins, and so is
less than the production of ATP (adenine triphosphate).</div>
<div style="text-align: justify;">
<br /></div>
<div class="jce_caption" style="display: inline-block; float: left; margin: 6px; width: 324px;">
<img alt="Figure-2" height="291" src="http://www.biot.it/site/images/stories/prodotti/papimi/figura-2.jpg" style="float: left;" width="324" />
<br />
<div class="jce_caption" style="text-align: left;">
<span style="color: maroon;">Figure 2</span>
The diagram shows the relationship between the concentration inside the
cell Na + ions and the potential trans-membrane associated, since they
are related to the health status of the cell. The device Papimi ® increases the TMP (Trans Membrane Potential) and decreases Natremia (concentration of Na-).</div>
</div>
<div style="text-align: justify;">
<span class="">All cellular
functions depend on the continued availability of energy derived from
catabolism of organic molecules during the process of cellular
respiration, the energy released is stored in the form of molecules of
ATP (adenosine triphosphate). </span>ATP is the energy reserves, readily available for all metabolic functions of the cell.</div>
<div style="text-align: justify;">
The electromagnetic field
generated by the device PAP IMI device is to act
directly at the cellular level, exploiting the natural ability of
biological structures interact with electromagnetic fields. It
is essentially to create resonances, as is now known, each substance
has its own characteristic electromagnetic spectrum, and any substance
interacts with electromagnetic waves is so non-specific (for example
through the transfer of energy) and specifically (interactions based on
the particular resonance frequency range).</div>
<div class="jce_caption" style="display: inline-block; float: right; width: 250px;">
<div class="separator" style="clear: both; text-align: center;">
<a href="http://www.biot.it/site/images/stories/prodotti/papimi/figura-3.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img alt="Figure-3" border="0" height="177" src="http://www.biot.it/site/images/stories/prodotti/papimi/figura-3.jpg" width="250" /></a></div>
<div style="text-align: left;">
<span style="color: maroon;">Figure 3</span>
The diagram shows the relationship between the concentration of
intracellular K + and Na + ions, since they are connected to the
trans-membrane potential and health status of the cells. The
device Papimi ® pushes the curve from the area in the lower right to
upper left area, where he represented the condition of young and healthy
cells.</div>
</div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
The membrane potential has a close relationship with the state of health of the cells. Under
physiological conditions this potential assumes a certain value which,
depending on the type of cell is between -70 and -90 mV. <span class="">This potential must be kept constant because the cell remains in physiology.</span></div>
<div style="text-align: justify;">
</div>
<div style="text-align: justify;">
So happens that, for
certain frequencies, the wave emitted by the device is able to interact,
resonating with the electromagnetic field produced by the cell. In addition, the cell membrane, by its very nature, conveys well the electromagnetic field.</div>
<div style="text-align: justify;">
</div>
<div style="text-align: justify;">
The effect of
electromagnetic pulse has features that allow you to restore the
membrane potential, altered by the pathological state. Moreover,
precisely due to its composition, the wave penetrates into the cell by
stimulating mitochondrial activity, cellular respiration and ATP
production.</div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
Therefore, at the cellular
level, it has a dual effect: stimulation of bio-electric nature, because
it restores the normal membrane potential was altered by the disease,
and stimulation of natural bio-chemistry, because the impulse is able to
penetrate inside the cell, which is to restore the physiology.</div>
<div style="text-align: justify;">
<br /></div>
<div style="text-align: justify;">
<a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com</a></div>
<div style="text-align: justify;">
</div>
<div style="text-align: justify;">
<a href="http://papimi.com/">http://papimi.com</a></div>
</div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-92087267039869161152011-10-05T23:52:00.000-07:002011-10-06T00:16:07.590-07:00Accelerated Treatment of Ankle Sprains<div dir="ltr" style="text-align: left;" trbidi="on">
<table border="0" cellpadding="10" cellspacing="0"><tbody>
<tr><td bgcolor="#FFFFFF" valign="top"><div align="center">
<span style="color: #0000a0; font-size: medium;">ACCELERATED TREATMENT OF ANKLE SPRAIN BY
APPLYING PAPIMI 600P BIOMAGNETIC GENERATOR, WITH CRYOTHERAPY AND PHYSICAL EXERCISES FOR
FOOTBALL PLAYERS.</span></div>
<div align="center">
<span style="font-size: medium;"><b>BY</b></span></div>
<div align="center">
<span style="font-size: medium;"><b>HOMIROS EMMANOUILIDIS<br />
Medical Doctor for Sports Injuries<br />
104 Kifisias Ave, Athens, Greece<br />
tel.:+301-6984321.</b></span></div>
<div align="center">
<br />
<center><table border="1" cellpadding="15" style="width: 585px;">
<tbody>
<tr>
<td bgcolor="#FFFFFF" width="551"><div align="center">
<span style="color: #800040;"><i><span style="font-size: medium;"><b>Dr. HOMEROS EMMANUILIDIS</b>, <br />
</span><span style="font-size: small;"><b>Specialist Medical Doctor For Sports,<br />
was born in Athens, and graduated from the Medical School of Athens University.<br />
Dr. Emmanuilidis has specialized in Sports Injuries in the School of Medicine at the
University of Athens, as well as he has specialized in Athletic Medicine in Italy.<br />
He coordinates the Soccer Team for the National Center of Athletic Research.<br />
He has been duty Medical Doctor for the major football teams of Greece:
"Panathinaekos", "Athens Apollon", as well as National Teams for
Elpidon Teenagers and Adult Men. .<br />
He has published many studies concerning football.</b></span></i></span></div>
</td>
</tr>
</tbody></table>
</center></div>
<div align="center">
<span style="color: #0000a0; font-size: large;"><i><b><u>Summary </u></b></i></span></div>
<span style="font-size: medium;">In the present report, we show a method we developed by applying the PAP
IMI Device - Bio Pulse Generator, for professional football players with ankle sprain, the
time of recovery for the injured players is significantly reduced. The method allows the
players to come back to their athletic obligations, in a significantly shorter time, which
is usually before their next athletic meeting or activity.</span><br />
<span style="font-size: x-small;">(</span>Short presentation is given below<span style="font-size: medium;"><b><u>)</u></b></span><br />
<div align="center">
<span style="color: maroon; font-size: large;"><i><b><u>INTRODUCTION</u></b></i></span></div>
<span style="font-size: medium;">The ankle arthrosis as well as the knee arthrosis are those that are
exposed to the biggest danger in a football match.</span><br />
<span style="font-size: medium;">The reasons, which create sprains of the ankle, are due to the direct
contact with the opponent, due to wrong balance during racing on rough surface or even due
to a loose arthrosis. Football players usually during their training, but, mainly at the
matches, back up their arthrosis with bandage or with self-adhesive elastic bandages using
the appropriate fascia. </span><br />
<span style="font-size: medium;">The goal of this research is to reduce the time of return to the match
for professional football player that was subject to an automatic second grade sprain or
after direct contact with an opponent had a second grade sprain.</span><br />
<span style="font-size: medium;">Sprain is the partial or the full brake of the fiber of one joint and
particularly of their outer portions, more specifically at the front portion which is
known as the perone ankle joint. It is an injury of resupination, adduction and is mainly
due to the anatomy of the foot end, because the internal melleolus is shorter than the
exterior melleolus and the arthrosis is less supported during an ectropic (with the foot
inwards) injury, forcing the outer sprain to accept all the weight of the load.</span><br />
<span style="font-size: medium;">Fewer times the opposite is happening - ectropia (with the foot
outwards) affecting in that way the outer elements of the ankle.</span><br />
<span style="font-size: medium;">The sprains are distinguished according to that gravity of the injury:
a) to the first grade or light sprain, b) to the second grade or heavy sprain with full
joint rhexis, c) third grade with full rhexis which concerns the medium of the joint,
which may have the form of detachment either from the gemma or from the sertion, either
with or without osteal fragma. With the rhexis of the conjunction, rhexis of the synovial
bursa occurs.</span><br />
<span style="font-size: medium;">Rhexis alone of the peroneal joint of the leg if not treated on time, it
may end to instability of the arthrosis. The same is true for the rhexis alone of the
outer later jont which can end to relapse sprain of the ankle , which implies astasia of
the arthrosis and it may end to possible degenerative arthritis. </span><br />
<span style="font-size: medium;">The active athlete after an injury has to terminate immediately the
athletic activity and should undertake medical and radiological check ups in order to
determine the gravity of the sprain.</span><br />
<span style="font-size: medium;">Clinically after some hours, the arthrosis is characterized by a huge
edema as well as by a huge hematoma. After such injury, intense pain and walking inability
occurs.</span><br />
<span style="font-size: medium;">For the second grade of sprain the proposed treatment is as following: </span><br />
<ul>
<li><span style="font-size: medium;">Applications of cold compresses for 15-20 minutes at frequent time
intervals for the first 48 hours. </span></li>
<li><span style="font-size: medium;">Functional fasciation with elastic bandages or functional splint,
"Air Castle" type, for 8-10 days. </span></li>
<li><span style="font-size: medium;">Upstream place of the leg. </span></li>
<li><span style="font-size: medium;">Avoidance of walking and tension of the part. </span></li>
<li><span style="font-size: medium;">Pharmaceutical treatment with anti-inflammatory and anti-edema
medication. </span></li>
<li><span style="font-size: medium;">At least 10 sessions of physiotherapy treatments after the 5<sup>th</sup>
day which include vortex bath, ultrasound, electrotherapy, massage cryotherapy,
reinforcement exercises of the ankle, proprietor exercises.</span></li>
</ul>
<span style="font-size: medium;">Total time for gradual coming back at the athletic activities is 15-20
days.</span><br />
<span style="font-size: medium;">For our pilot research we finally selected 20 football players who had
second grade sprain, either automatic or because of an "opponents’ contact".</span><br />
<span style="font-size: medium;">Clinically the injured players under our study, presented a tense edema
and hematoma. The x-rays analysis was negative for fracture. For 3 occasions that was
determined necessary they were examined under "static movement" check up, which
resulted negative for a fully break of the joint.</span><br />
<div align="center">
<br /></div>
<div align="center">
<span style="color: maroon; font-size: large;"><i><b><u>METHOD</u></b></i></span></div>
<span style="font-size: medium;">The ankle was immobilized with “Air castle splint" and cold
compresses were applied for 24 hours. The second 24 hours they received treatments with a
PAP-IMI 600P Magnetic Pulser Device. The PAPIMI treatments were twice every morning as
well as every evening for 20 minutes’ duration each.</span><br />
<span style="font-size: medium;">The device produces: </span><br />
<ul>
<li><span style="font-size: medium;">Complex magnetic induction field as it is shown in the oscillogram with
continuously reducing intensity during every complex pulse, with an initial instantaneous
peak of 10,000 ampere-turns max, which corresponds to 125 gauss, modulated from
oscillations of excited gaseous plasma with PAP- IMI method. </span></li>
<li><span style="font-size: medium;">The overall duration of every complex pulse is 10 microseconds, repeated
every 500ms. </span></li>
<li><span style="font-size: medium;">The energy at every complex pulse is of the range of 54 Joules. </span></li>
<li><span style="font-size: medium;">The average potential of the field 2x54 Joules/or 108 watts. </span></li>
<li><span style="font-size: medium;">The frequency consists of continuous harmony Fourier components from 0.3
MHZ to 250 MHZ. </span></li>
<li><span style="font-size: medium;">Effective penetration is 15 cm at full potential, reduced proportionally
with the third power of the distance.</span></li>
</ul>
<span style="font-size: medium;">After the treatment, cold compresses were applied for 15 minutes and the
functional splint was placed back. The edema was reduced greatly after the second
treatment. The football players began light running exercises on the fourth day after the
injury, with their splints completely removed.</span><br />
<span style="font-size: medium;">The same day, they started special reinforcement exercises for the
ankle.</span><br />
<div align="center">
<br /></div>
<div align="center">
<span style="color: maroon; font-size: large;"><i><b>RESULTS</b></i></span></div>
<span style="font-size: medium;"><b>60% </b>of the football players recovered completely the 6<sup>th</sup>
day and returned to their athletic obligations.<br />
Recovery reduction time was down to 30%.</span><br />
<span style="font-size: medium;"><b>30%</b> of the football players recovered the 8<sup>th</sup> day
after the injury.<br />
Recovery reduction time was down to 44%.</span><br />
<span style="font-size: medium;"><b>10<sup> </sup>%</b> of the football players were feeling annoyance at
the 10<sup>th</sup> day. <br />
In this case, the two players remaining (20x10%=2) recovered the 13<sup>th</sup> and 14<sup>th</sup>
day accordingly. <br />
Recovery reduction time was down to 75%.<br />
Pharmaceutical treatment was not given at all.</span><br />
<span style="font-size: medium;">Conclusively: We have proven that the method -by applying the PAP IMI
Device - Bio Pulse Generator - for football players with second grade sprain of the ankle,
the time of recovery was significantly reduced and allowed the players to come back to
their athletic activities in a much shorter time and before the next weekly match.</span><br />
<br />
<div align="center">
<span style="color: maroon; font-size: medium;">***************</span></div>
<br />
<span style="font-size: medium;"><i><b>Notice 1.</b></i></span><br />
<span style="font-size: medium;"><b>We have distinguished the injuries in four different categories </b></span><br />
<ul>
<li><span style="font-size: medium;">In the first category we distinguished the type of the injury (automatic
muscle injury from cicatrices, injury of arthrosis).</span></li>
<li><span style="font-size: medium;">In the second category we determined the point of trauma to establish
whether some parts of the body are more fender.</span></li>
<li><span style="font-size: medium;">In the third category we distinguished the time periods that the injuries
were occurred (preliminary training, climate conditions, tense match obligations)</span></li>
<li><span style="font-size: medium;">In the fourth category we noted the number of the pathological cases
during the match period.</span></li>
<li><span style="font-size: medium;">The total number of the football players that were included at this
research was 68.</span></li>
<li><span style="font-size: medium;">Due to the longer time of non-participation to local matches during the
last summer period, because of the World Championship, there was enough time to most
chronic injuries to cure. The time of the preliminary training was prolonged. So the
training period was increased smoothly and there were no actual new injuries.</span></li>
<li><span style="font-size: medium;">For a team that worked less hard at the beginning, giving friendly
matches more sprains occurred later during the championship.</span></li>
</ul>
<span style="font-size: medium;"><i><b>Notice 2.</b></i> </span><br />
<ul>
<li><span style="font-size: medium;">For teams that had more matches’ participations (championships, links,
national obligations) more muscular injuries and knee’s injuries occurred, mainly at the
period of the increased matches’ obligations.</span></li>
<li><span style="font-size: medium;">For a team that is trying to remain at one category and which does not
have a permanent area of training, more injuries are observed to occur for the ankle
during the rain period when stadiums are usually in bad conditions. Also an increase of
automatic muscle injuries occurs after the change of the coach or after the change of the
training type. </span><span style="font-size: x-small;"> </span></li>
</ul>
<blockquote>
<blockquote>
http://papimiuk.blogspot.com</blockquote>
</blockquote>
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papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-17268944053984748942011-10-05T23:32:00.000-07:002011-10-05T23:36:05.222-07:00Application Of The PAPIMI Device On Plants - Comparison Results<div dir="ltr" style="text-align: left;" trbidi="on">
<div align="center" style="color: blue;">
<span style="font-size: x-large;">C</span><span style="font-size: large;">OMPARISON RESULTS<br />
Exposed Plants with twin Plants Non Exposed <br />
for about 10 minutes exposures every other day</span><i><b><span style="font-family: Arial; font-size: x-large;"><a href="http://whos.amung.us/stats/i5tj56aji19t/"><span style="text-decoration: none;"><img border="0" height="2" src="http://whos.amung.us/widget/i5tj56aji19t.png" title="Click to see how many people are online" width="5" /></span></a></span></b></i><b><span style="font-size: small;"> </span></b></div>
<div align="center" style="color: blue;">
<br /></div>
<div align="center">
<b><span style="color: black; font-size: small;">Experiments carried by Nick Vavlis<br />
19, Maggnisias Street, Nea Smyrna, (Athens), Greece, 17121<br />
Tel.: +301-9324370</span><br />
<span style="color: #800040; font-size: medium;">****</span></b><br />
<span style="color: #2f2f5e; font-size: medium;">More pictures will be posted as the experiments progress.</span><br />
<span style="color: #800040; font-size: medium;"><b>****</b></span></div>
<div align="center">
<br />
<br />
<center><table border="0" cellpadding="0" cellspacing="5" style="width: 753px;">
<tbody>
<tr>
<td align="center" valign="top"><table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e;"><span style="font-size: medium;">Sowing Peas Seeds, Day 1<br />
</span><img height="283" src="http://papimi.gr/p005.jpg" width="229" /></span></td>
</tr>
</tbody></table>
</td>
<td align="center" valign="top"><table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><div align="center">
<br />
<br />
<center><table border="0" cellpadding="0" cellspacing="0">
<tbody>
<tr>
<td height="44" width="100%"><div align="center">
<span style="color: #2f2f5e; font-size: medium;">Sowing Peas,
X Day after</span></div>
</td>
</tr>
<tr>
<td><div align="center">
<span style="color: black; font-size: medium;"><b><img height="165" src="http://papimi.gr/cases/plants35.jpg" width="150" /></b></span></div>
</td>
</tr>
<tr>
<td height="41" width="100%"><div align="center">
<span style="color: #055850; font-size: small;">Exposing
sowing peas with PAP IMI Probe</span></div>
</td>
</tr>
</tbody></table>
</center></div>
</td>
</tr>
</tbody></table>
</td>
<td align="center" valign="top"><table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><table border="0" cellpadding="0" cellspacing="0">
<tbody>
<tr>
<td width="100%"><div align="center">
<span style="color: #2f2f5e; font-size: medium;">Sowing Beans after X Day
Exposures</span></div>
</td>
</tr>
<tr>
<td width="100%"><div align="center">
<span style="color: #2f2f5e; font-size: medium;"><b><img height="192" src="http://papimi.gr/cases/plants34.jpg" width="149" /></b></span></div>
</td>
</tr>
<tr>
<td width="100%"><div align="center">
<span style="color: #055850; font-size: small;">Exposing sowing beans
with PAP IMI Probe</span></div>
</td>
</tr>
</tbody></table>
</td>
</tr>
</tbody></table>
</td>
</tr>
</tbody></table>
</center></div>
<div align="center">
<br />
<br />
<center><table border="0" cellpadding="10" cellspacing="0">
<tbody>
<tr>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Beans, 9 Day<br />
</span><span style="color: black; font-size: medium;"><b><img height="162" src="http://papimi.gr/plants20.jpg" width="250" /></b></span><span style="color: #055850; font-size: small;"><b><br />
</b>2. After Exposed to PAP IMI and watered with activated water, it grows faster.<br />
1. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Peas, 14 Day<br />
</span><span style="color: black; font-size: medium;"><b><img height="163" src="http://papimi.gr/plants23.jpg" width="250" /></b></span><span style="color: #055850; font-size: small;"><b><br />
</b>1. After Exposed to PAP IMI and watered with activated water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
</tr>
<tr>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Peas, 14 day<br />
</span><span style="color: black; font-size: medium;"><b><img height="213" src="http://papimi.gr/plants22.jpg" width="249" /></b></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with activated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Beans, 17 day<br />
</span><span style="color: black; font-size: medium;"><b><img height="213" src="http://papimi.gr/plants40.jpg" width="250" /></b></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with activated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
</tr>
<tr>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Peas, 17 Day<br />
</span><span style="color: black; font-size: medium;"><b><img height="190" src="http://papimi.gr/plants39.jpg" width="250" /></b></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with activated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Peas, 17 Day<br />
</span><span style="color: black; font-size: medium;"><b><img height="190" src="http://papimi.gr/plants38.jpg" width="250" /></b></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with activated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
</tr>
<tr>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Beans, 17 Day<br />
</span><span style="color: black;"><img height="192" src="http://papimi.gr/plants37.jpg" width="250" /></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with actvated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
<td width="50%"><br />
<table border="1" height="300" style="width: 230px;">
<tbody>
<tr>
<td width="100%"><span style="color: #2f2f5e; font-size: medium;">Sowing Beans, 17 Day<br />
</span><span style="color: black; font-size: medium;"><b><img height="192" src="http://papimi.gr/plants36.jpg" width="250" /></b></span><br />
<span style="color: #055850; font-size: small;">1. After Exposed to PAP IMI and watered with activated
water, it grows faster.<br />
2. After Watered with non activated water and not exposed.</span></td>
</tr>
</tbody></table>
</td>
</tr>
</tbody></table>
</center></div>
<table border="0" cellpadding="10" cellspacing="0">
<tbody>
<tr>
<td width="100%"><div align="center">
<span style="color: #800040;">C<span style="font-size: large;">ONCLUSION</span></span><br />
<span style="color: #800040; font-size: medium;">All Plants exposed to PAP IMI pulses grow significantly
faster in comparison to twin non exposed plants.</span></div>
</td>
</tr>
</tbody></table>
<div style="text-align: center;">
<span style="color: #055850; font-size: medium;">Sowing Beans after one Month</span></div>
<span style="color: #055850; font-size: medium;"><br /></span><br />
<div style="text-align: center;">
<span style="color: #055850; font-size: medium;">
</span><span style="color: black; font-size: medium;"><img height="274" src="http://papimi.gr/Graphic1.jpg" width="300" /></span></div>
<span style="color: black; font-size: small;">Both plants, exposed (white pot) and non exposed (black
pot) developed to about the same size finally after a month, indicating their DNA growth
schedule developed the same for both seeds exposed and non exposed. However, the exposed
plant grew up much faster, too, as it was indicated in the previous pictures. Nevertheless
the new clones of second generation of the exposed plant in the white pot grow
significantly taller and faster. Experiments are in progress 14/4/1999</span><br />
<br />
<div style="color: black; text-align: center;">
<span style="font-size: x-large;">C</span><span style="font-size: large;">OMPARISON RESULTS</span><span style="font-size: x-large;"><br />
</span><span style="font-size: large;">Seeds watered by "activated" pure water <br />
by 5 minutes PAP IMI exposures,<br />
Seeds watered with pure water - not activated.</span></div>
<div style="color: black; text-align: center;">
<br /></div>
<table border="0" cellpadding="0" cellspacing="5" style="margin-left: auto; margin-right: auto; text-align: left;"><tbody>
<tr><td valign="top" width="50%"><div align="left">
<span style="color: black;"><img height="239" src="http://papimi.gr/p004.jpg" width="184" /></span><br />
<span style="color: #055850; font-size: small;">Activating water in a jar with PAP IMI Probe for watering
seeds</span><span style="color: black; font-size: small;">.</span></div>
</td>
<td valign="middle" width="50%"><div align="left">
<span style="color: black; font-size: medium;"><b><img height="179" src="http://papimi.gr/plants27.jpg" width="250" /></b></span><br />
<br /></div>
<div align="left">
<span style="color: #055850; font-size: small;">Activating water in a cup with PAP IMI
Probe for watering seeds.</span></div>
</td>
</tr>
<tr>
<td valign="top" width="50%"><div align="left">
<span style="color: #2f2f5e; font-size: medium;">Beans 7 Day<b><br />
</b></span><span style="color: black; font-size: x-large;"><img height="130" src="http://papimi.gr/plants01.jpg" width="239" /></span><br />
<span style="color: black; font-size: small;">1. Watered with Activated water. <br />
2. Watered with Non Activated water.</span></div>
</td>
<td valign="top" width="50%"><div align="left">
<span style="color: #2f2f5e; font-size: medium;">Beans 7 Day<b><br />
</b></span><span style="color: black; font-size: x-large;"><img height="130" src="http://papimi.gr/plants03.jpg" width="250" /></span><br />
<span style="color: black; font-size: small;">1. Watered with Non Activated Pure Water. <br />
2. Watered with Activated Pure Water</span></div>
</td>
</tr>
<tr>
<td valign="top" width="50%"><div align="left">
<span style="color: #2f2f5e; font-size: medium;">Lentis 6 Day<br />
</span><span style="color: black; font-size: x-large;"><img height="150" src="http://papimi.gr/plants02.jpg" width="250" /></span><br />
<span style="color: black; font-size: small;">1. Watered with Activated Pure Water. <br />
Stays clear.<br />
2. Watered with Non Activated Pure Water. <br />
Gets rotten.</span></div>
</td>
<td valign="top" width="50%"><div align="left">
<span style="color: #2f2f5e; font-size: medium;">Hard Wheat 6
Day<b><br />
</b></span><span style="color: black; font-size: x-large;"><img height="150" src="http://papimi.gr/plants04.jpg" width="250" /></span><br />
<span style="color: black; font-size: small;">1. Watered with Activated Pure Water. <br />
It never gets rotten.<br />
2. Watered with Non Activated Pure Water. <br />
It gets rotten by the 13th day.</span></div>
</td>
</tr>
<tr>
<td colspan="2" valign="top" width="100%"><div align="center">
<span style="color: #2f2f5e; font-size: medium;">Lentils
27 Day<b><br />
</b></span><span style="color: black; font-size: x-large;"><img height="154" src="http://papimi.gr/plants05.jpg" width="250" /></span><br />
<span style="color: black; font-size: small;">1. Watered with Non Activated Pure Water. <br />
Finally, both seeds develop at the same hight.<br />
2. Watered with Activated Pure Water. <br />
Much Harder, slightly taller, and developed much quicker.</span></div>
</td>
</tr>
</tbody></table>
<div>
</div>
<div style="text-align: center;">
<span style="color: #800040; font-size: medium;">Seeds watered with activated
pure water grow faster and taller.</span></div>
<div style="text-align: center;">
</div>
<div style="text-align: center;">
<span style="color: #800040; font-size: medium;">Seeds watered with activated water tend to
get rotten and to develop parasites, significantly less, compared to the seeds watered
with non exposed pure water.</span></div>
<div style="color: blue; text-align: center;">
<br /></div>
<div style="color: black; text-align: center;">
<span style="color: white;"><span lang="EN-US"><span style="font-size: x-large;">A</span><span style="font-size: large;">PPLICATION OF THE PAPIMI DEVICE <br />
IN </span><span style="font-size: x-large;">P</span><span style="font-size: large;">LANTS.</span></span></span><span style="font-size: large;"><span style="color: blue;"> </span></span></div>
<div style="text-align: center;">
<br /></div>
<table border="0" cellpadding="10" cellspacing="0"><tbody>
<tr><td align="center" bgcolor="#FFFFFF" width="100%"><div align="left">
<span lang="EN-US"><big><big>P</big></big>AP IMI device has unbelievable
results in the growth of plants and seeds. Bibligraphy has</span> <span lang="EN-US"> </span>references to similar cases in
growing of plants using magnetic pulses. The results as well as previous evidences, were
not always replicable, and some results failed to work in practical applications. On the
contrary the results of the PAP IMI device in plants are replicable and significant, as
this is proved in related research by the Agriculture University of Athens. In addition
there did not appear any genetic anomalies, toxicity or harm in the exposed plants, on the
contrary it proved to be very effective in speeding up the growth of plants, even under
unfavorable conditions that did not surpass the expected mainsail growth of the plants.
Related results have also been found for three years in succession by the<span style="color: navy;"> <big>P</big>apnikolau <big>I</big>nstitute of the <big>H</big>ospital <big>S</big>aint,
<big>S</big>avva,</span> in small animals that grew up and multiplied to serial
generations, without genetic or other anomalies.</div>
<div align="center" class="MsoNormal" style="text-align: justify;">
<span lang="EN-US"><big><big>T</big></big>he
Agriculture University of Athens continues the research on practical application with the
PAP IMI device in the grouth of plants and seeds. Related dissertations are the most
elaborate cooperation with the<span style="color: #804000;"> </span><span style="color: navy;"><big>E</big>ducational
and <big>T</big>echnologic <big>I</big>nstitute of <big>P</big>irea</span><span style="color: #804000;">.</span></span></div>
<div align="center" class="MsoNormal" style="text-align: justify;">
<span lang="EN-US"><big><big>B</big></big>elow
are shown photos of experiments on the grouth of plants and seeds using the PAP IMI
device. Each experiment lasts for about 5 minutes to 1 hour.</span></div>
</td>
</tr>
<tr align="center">
<td align="center" bgcolor="#FFFFFF" width="100%"><img border="0" height="495" src="http://papimi.gr/cases/plants1.jpg" width="490" /></td>
</tr>
<tr align="center">
<td align="center" bgcolor="#FFFFFF" width="100%"><img border="0" height="336" src="http://papimi.gr/cases/plants2.jpg" width="562" /></td>
</tr>
<tr align="center">
<td align="center" bgcolor="#FFFFFF" width="100%"><div align="center">
<img border="0" height="489" src="http://papimi.gr/cases/plants3.jpg" width="567" /></div>
</td>
</tr>
<tr align="center">
<td align="center" bgcolor="#FFFFFF" width="100%"><div align="center">
<img border="0" height="379" src="http://papimi.gr/cases/wpe4.gif" width="632" /> </div>
<div align="center">
<br /></div>
<div align="center">
Source : <a href="http://www.papimi.gr/">www.papimi.gr</a></div>
<div align="center">
<a href="http://www.papimiuk.blogspot.com/">www.papimiuk.blogspot.com</a></div>
</td></tr>
</tbody></table>
</div>
papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-3417955596399663472011-10-05T23:20:00.000-07:002011-10-05T23:20:58.648-07:00Lightning Bolts within Cells<div dir="ltr" style="text-align: left;" trbidi="on">
<h3>
Lightning Bolts within Cells</h3>
<div class="intro">
A new nanoscale tool reveals strong electric fields inside cells.</div>
<br />
Using novel voltage-sensitive nanoparticles, researchers have found
electric fields inside cells as strong as those produced in lightning
bolts. Previously, it has only been possible to measure electric fields
across cell membranes, not within the main bulk of cells. It's not clear
what causes these strong fields or what they might mean. But now that
it's possible to measure them, researchers hope to learn about disease
states such as cancer by studying these electric fields.<br />
<br />
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<a href="http://1.bp.blogspot.com/-i5_pHALsfB0/To1HHWB9VjI/AAAAAAAAABY/vJGIzdH6Pb8/s1600/biophys_x220.jpg" imageanchor="1" style="margin-left: 1em; margin-right: 1em;"><img border="0" height="320" src="http://1.bp.blogspot.com/-i5_pHALsfB0/To1HHWB9VjI/AAAAAAAAABY/vJGIzdH6Pb8/s320/biophys_x220.jpg" width="186" /></a></div>
<div class="caption">
<b>The cell electric:</b> Encapsulated in a polymer shell just 30
nanometers across, voltage-sensitive dyes (red) emit red and green light
when illuminated with blue light. These encapsulated dyes make it
possible to measure electric fields inside cells.
<br />
<span class="credit">Raoul Kopelman, University of Michigan</span>
</div>
<br />
University of Michigan researchers led by chemistry professor <a href="http://www.umich.edu/%7Ekoplab/raoul_kopelman.html" target="_blank">Raoul Kopelman</a>
encapsulated voltage-sensitive dyes in polymer spheres just 30
nanometers in diameter. When illuminated with blue light, the
voltage-sensitive dyes emit a mixture of red and green light; the exact
frequency of light emitted is influenced by the strength of local
electric fields, allowing the researchers to measure those fields.
Testing these nanoparticles in the internal fluid of brain-cancer cells,
Kopelman found electric fields as strong as 15 million volts per meter,
perhaps five times stronger than the field found in a lightning bolt.<br />
<br />
"They have developed a tool that allows you to look at cellular changes on a very local level," says <a href="http://nano.cancer.gov/about_alliance/bios_alliance.asp#Grodzinski" target="_blank">Piotr Grodzinski</a>, director of the National Cancer Institute <a href="http://nano.cancer.gov/" target="_blank">Alliance for Nanotechnology in Cancer</a>.
Traditional techniques for studying disease at the level of tissues
average out differences between cells. Grodzinski says that many
developments in cancer research over the past few years have been "more
reactive," working toward developing diagnostics for catching the
disease in its earlier stages and for better predicting to which drugs
patients will respond. Despite how far cancer treatments have come, the
way that cancer progresses at the cellular level is still not very well
understood. With a better understanding, researchers hope to further
improve diagnostics and personalized care. "This development represents
an attempt to start using nanoscale tools to understand how disease
develops," says Grodzinski.<br />
<br />
<a href="http://nano.cancer.gov/about_alliance/bios_alliance.asp#Lee" target="_blank">Jerry S.H. Lee</a>,
a nanotechnology project manager also at the National Cancer Institute,
says that Kopelman's research bolsters the set of nanoscale tools that
scientists are developing to probe cells' physical properties, such as
special microscopic probes for measuring cell stiffness. (See "<a href="http://www.technologyreview.com/Nanotech/19808/" target="_blank">The Feel of Cancer Cells</a>.")
In the past decade, researchers have improved cancer diagnosis by
examining protein markers and genetic signatures. Now they're "thinking
of how nanotechnology can make tools to look at additional signatures"
like electric fields, says Lee.<br />
<br />
Voltage-sensitive dyes are not new. For decades, neuroscientists
have used them to measure voltages across cell membranes in studies of
how nerve cells generate and respond to electrical charges. But Kopelman
says that it's not possible to control the placement of these dyes in
cells. They are hydrophobic and aggregate in cell membranes, so it has
not been possible to use them to study the cytosol, the bulk of the
interior of the cell. Kopelman also says that these dyes might be
reacting with enzymes and other molecules in cells. His encapsulated
dyes aren't hydrophobic and can operate anywhere in the cell, not just
in membranes. Because it's possible to place his encapsulated dyes in a
cell with a greater degree of control, Kopelman likens them to
voltmeters. "Nano voltmeters do not perturb [the cellular] environment,
and you can control where you put them," he says.<br />
<br />
The existence of strong electric fields across cellular membranes is
accepted as a basic fact of cell biology. Maintaining gradients of
charged molecules and ions allows for many cellular functions, from
control over cell volume to the electrical discharges of nerve and
muscle cells.<br />
<br />
The fact that cells have internal electric fields, however, is
surprising. Kopelman presented his results at the annual meeting of the <a href="http://www.ascb.org/" target="_blank">American Society for Cell Biology</a> this month. "There has been no skepticism as to the measurements," says Kopelman. "But we don't have an interpretation."<br />
<a href="http://depts.washington.edu/chem/people/faculty/chiu.html" target="_blank">Daniel Chu</a>
of the University of Washington in Seattle agrees that Kopelman's work
provides proof of concept that cells have internal electric fields.
"It's bound to be important, but nobody has looked at it yet," Chu says.<br />
<br />
Grodzinski says that an interesting application of the
voltmeters will be to examine whether there's a difference in electrical
signals between healthy and diseased cells, and whether different disease
stages might have characteristic electrical signatures. To gauge the viability
of the technique, researchers will need to "start tying it to biology by
studying cell lines from the clinic," says Grodzinski. "This is a first
demonstration."<br />
<br />
<br />
Source: <a href="http://www.technologyreview.com/Biotech/19841/page1/%20">http://www.technologyreview.com/Biotech/19841/page1/ </a><br />
<a href="http://www.blogger.com/goog_149792079"><br /></a><br />
<a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com</a></div>
papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-92104159825049653962011-10-02T20:39:00.000-07:002011-10-02T21:01:08.019-07:00The Secrets of Papimi Water<div dir="ltr" style="text-align: left;" trbidi="on">
<div align="center">
<a href="http://www.papimi.gr/MRI_scan.htm"><i><b>UNDISPUTABLE SCIENTIFIC EVIDENCE ABOUT THE NON CHEMICALLY ENERGIZED PAPIMI WATER<span style="font-family: Arial Black; font-size: large;"> click here to see relevant pictures</span></b></i></a></div>
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<br /></div>
<span style="font-size: large;"><i><b>NEW BREAKTHROUGH FACTS:</b></i><br />The scientific objectiveness of the energized PAPIMI water can be shown by MRI Magnetic Resonance Imaging. MRI is the most advanced diagnostic imaging technique in medicine, used widely today.</span><br />
<span style="font-size: large;">With the following experiment:<br />Seven identical sealed bottles with the same distilled water are prepared, the 2 of the 7 bottles are exposed 20 minutes with the PAPIMI probe. Then, the same thing is repeated with the other 2 bottles, but exposure time now is 10 minutes. 3 bottle are left without any exposure.</span><br />
<span style="font-size: large;">Then all 7 bottles, about six hours later, are brought to an MRI Center, placed simultaneously and one next to the other in the MRI chamber to be photographed.<br /><br />Results:</span><br />
<br />
<span style="font-size: large;">All 3 Bottles without exposure at all comes out dark</span><br />
<span style="font-size: large;">All 2 Bottles exposed 20 minutes comes out bright</span><br />
<span style="font-size: large;">All 2 Bottle exposed 10 minutes comes out </span><b><span style="font-size: x-large;"> </span></b><span style="font-size: large;">half bright</span><br />
<br />
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<br />
THE SECRETS OF PAPIMI WATER<br />
<br />
<b><span style="color: red; font-size: x-large;">IN ALL CASES <br />DRINK AS MUCH AS YOU CAN PAPIMI ENERGIZED WATER<br />energize your body with papimi energized water<br />and feel the power</span></b></div>
<br />
<span style="font-size: x-large;"><b>NEW</b></span><b><span style="font-size: x-large;"> PAPPAS' SCIENTIFIC BREAKTHROUGH PROOF FOR NON CHEMICAL PROPERTIES OF WATER:<br /> <br />"SOME WATER PROPERTIES ARE NOT DETERMINED BY ITS CHEMICAL COMPOSITION BUT ALSO DEPEND ON ITS PREVIOUS MAGNETIC TREATMENT THAT DOES NOT ALTER ITS CHEMICAL COMPOSITION"</span></b><br />
<span style="font-size: x-large;">THE HYPOTHESIS OF CRYSTAL WATER</span><span style="font-size: medium;"><b> <a eudora="autourl" href="http://www.theresedilor.com/esther.html">http://www.theresedilor.com/esther.html</a></b></span><span style="font-size: large;"> by Dr. Esther Del Rio.</span><span style="font-size: x-large;"> </span><br />
<span style="font-size: large;">Liquid water can form icosahedral water clusters :</span><span style="font-size: medium;"> </span><a eudora="autourl" href="http://www.lsbu.ac.uk/water/abstrct.html"><span style="font-size: medium;">http://www.lsbu.ac.uk/water/abstrct.html</span></a><br />
<span style="font-size: medium;">Water effects on health : References <a href="http://www.papimi.gr/nero.htm">www.papimi.gr/nero.htm</a> </span><br />
<b><span style="font-size: x-large;"><br />TREATING WATER WITH PAPIMI</span></b><br />
<span style="font-size: large;">There seems to be two ways of transferring the benefits of papimi.</span><br />
<span style="font-size: large;">The first way is to apply the probe over the object one wants to transfer the benefit.</span><br />
<span style="font-size: large;">The second way is to treat the water that will be watering the plants. </span><b><a href="http://www.papimi.gr/plantpic.htm"><span style="font-size: medium;">http://www.papimi.gr/plantpic.htm</span></a></b><br />
<br />
<span style="font-size: medium;"></span><span style="font-size: 22pt; font-weight: 700;">See among the numerous experiments, the substantial difference in growth with and without papimi activated water.</span><br />
<span style="font-size: large;"><b>The PAPIMI activated water.</b> <b><img border="0" height="199" src="http://www.papimi.gr/treat10a.jpg" width="89" /> was given to the pot with white label with beans seeds</b> <img border="0" height="200" src="http://www.papimi.gr/treat10b.jpg" width="143" /> <b>After 9 days six seeds have developed considerably.</b></span><br />
<br />
<b> </b><span style="font-size: large;"><b>Normal water</b>. <b><img border="0" height="178" src="http://www.papimi.gr/untreat10a.jpg" width="92" /> was given to the next pot with the same number of beans seeds </b><img border="0" height="199" src="http://www.papimi.gr/untreat10b.jpg" width="142" /> <b>After 9 days one seed is just underdeveloped.<br /> </b></span><br />
<span style="font-size: large;"><b>This experiment was repeated by us many times and the Agricultural University of Athens (AUA) with hundreds of plants and always with the same results. </b></span><br />
<br />
<span style="font-size: large;"><b>See confirming letter of AUA below.</b></span><br />
<i><b><a href="http://www.papimi.gr/Efthimiadis_2003.jpg"><img border="0" height="358" src="http://www.papimi.gr/Efthimiadis_2003.jpg" width="263" />clicktoenlarge</a> <a href="http://www.papimi.gr/Efthimiadis_2003eng.jpg"><img border="0" height="374" src="http://www.papimi.gr/Efthimiadis_2003eng.jpg" width="290" />clcktoenlarge </a> </b></i><br />
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<b><a href="http://www.papimi.gr/plantpic.htm">COMPARISON RESULTS : </a></b></div>
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<b><a href="http://www.papimi.gr/plantpic.htm">Exposed Plants with twin Plants Non Exposed for about 10 minutes exposures every other day. http://www.papimi.gr/plantpic.htm </a></b></div>
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<span style="font-size: large;"><img border="0" height="199" src="http://www.papimi.gr/plants23.jpg" width="294" /> <br /><br /> </span></div>
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<b><span style="font-size: large;">Also, see the typical difference between the plant (peas) growth given activated water (white label on the pot), and the similar plant given normal water, after 14 days</span></b><i><b><span style="font-family: Arial; font-size: x-large;"><a href="http://whos.amung.us/stats/i5tj56aji19t/"><span style="text-decoration: none;"><span style="color: white;"><img border="0" height="2" src="http://whos.amung.us/widget/i5tj56aji19t.png" title="Click to see how many people are online" width="5" /></span></span></a></span></b></i></div>
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<span style="font-size: large;">By</span><span style="font-size: large;"> treating water in shielded plastic bottles as shown, at then to apply or supply the water, if possible, to the object. Hundreds of experiments like this at our Laboratories as well at the Agricultural University of Athens, has shown that something is indeed stored in the water that provides similar or better results as in the first way, by drinking the treated water, by watering plants, etc. <br /><br />PAPIMI treated water seems to act as the so called crystal water. Analysis and comparisons of the PAPIMI WATER and CRYSTAL WATER </span><span style="font-size: medium;"><b><a eudora="autourl" href="http://www.theresedilor.com/esther.html">http://www.theresedilor.com/esther.html</a></b></span><span style="font-size: large;"> by Dr. Esther Del Rio is on the way and we shall reports the results here as soon as they are conclusive.</span><br />
<span style="font-size: large;">What is certain now and here is not all the properties of the water are due to its chemical composition. More beneficial properties seem to be due perhaps to a so called crystalline structure of the water of 37 molecules, which primarily affect biological shaping of plants and animals. <br /><br />FOR EXAMPLE<br /> </span><br />
<span style="font-size: large;">PAPIMI WATER watering plants develops these plants to their maximum height from seeds several times faster.</span><br />
<span style="font-size: large;">PAPIMI WATER seem to enable the eliminations of scars due to wounds, burns, or even marks due to tumor as direct PAPIMI EXPOSURE seem to do. <br /><br />Professor <br />Panos Pappas, <br />PhD Physics.</span><br />
<br />
<div align="center">
<span style="font-size: large;"> </span>TREATING AND ENERGIZING <br />
WATER WITH PAPIMI</div>
<img border="0" height="236" src="http://www.papimi.gr/papimibottle.jpg" width="312" /><br />
<br />
<img border="0" height="254" src="http://www.papimi.gr/water3.jpg" width="315" /><br />
<br />
<img border="0" height="221" src="http://www.papimi.gr/water2.jpg" width="313" /><br />
<br />
<br />
<span style="font-size: x-large;">USING PAPIMI AND PAPIMI WATER</span><span style="font-size: medium;"><br /></span><span style="font-size: x-large;">SYNERGETICALLY TO ELIMINATE FOOT MARKS<br /> </span><br />
<img border="0" height="224" src="http://www.papimi.gr/papimiwater1.jpg" width="313" /><br />
<span style="font-size: medium;">Important Notice: A plastic container, a ground and an insulated chair are required as shown, for safety to act independently of the safety leakage controls of papimi device (0.3ma new devices, 3ma older devices).</span><span style="font-size: x-large;"> </span>Otherwise and better, you may use papimi device first and then papimi water, or the other way around, afterwards and separately.<br />
<b><span style="color: red; font-size: x-large;">IN ALL CASES <br />DRINK AS MUCH AS YOU CAN PAPIMI ENERGIZED WATER<br />AND FEEL THE POWER</span></b><br />
<br />
<strong><span style="color: red;">Source <a href="http://www.papimi.gr/">http://www.papimi.gr/</a></span></strong><br />
<br />
<strong><span style="color: red;"><a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com/</a></span></strong></div>
papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-64541480517823236052011-10-02T20:21:00.000-07:002011-10-02T20:24:02.305-07:00PAPIMI Testimonials<div dir="ltr" style="text-align: left;" trbidi="on">
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<b><span lang="EN-US" style="font-family: Arial; font-size: 14pt;">Athlete suffering from chondropathia after being treated with PAPIMI device </span></b></div>
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<b><span lang="EN-US" style="font-family: Arial; font-size: 14pt;">plus chondroitine and glucozamine wins the Copper Medal ! </span></b></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">by Dr. Nick Papandreou M.D.</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">Female athlete A.S 38 years old came in my practice a wile ago diagnosed as suffering from chondropathia<b> </b>of the knee</span><span lang="EN-GB"><strong><b><i><a href="http://whos.amung.us/stats/i5tj56aji19t/"><span style="font-family: Arial; font-size: x-large;"><img border="0" height="2" src="http://whos.amung.us/widget/i5tj56aji19t.png" title="Click to see how many people are online" width="5" /></span></a></i></b></strong></span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">Patient was exposed in the pulsed magnetic field of the PAPIMI device around two or three times per week, for 30 minutes each time for one year. During this treatment she received also chondroitine and glucozamine as food supplements. </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">The results were outstanding, since in the athletic event "Olympus Marathon 2007" she won the Copper Medal ! </span></div>
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<b><span lang="EN-US" style="font-family: Arial; font-size: 14pt;">Application of PAPIMI device and antioxidants to primary hepatoma</span></b></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">by Dr. Nick Papandreou MD.</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">A 88 years old male patient came to my practice about one and a half year ago diagnosed with primary hepatoma. From then on, he has been exposed to the pulsed magnetic field of PAPIMI device three times per week, for 30 minutes each time and at the same time he was taking vitamins and antioxidants as food supplements. </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 14pt;">Here follows a partial record of the observed findings :</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Date </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Examination </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Findings </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">08/08/2006 </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Calculating Tomography</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 8cm diameter</span></div>
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<br /></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>22/09/2006</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A-Fetoprotein (AFP) </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">60500,0 ng / ml (reference values: 0,0 – 15,0) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">07/11/2006 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A-Fetoprotein (a-FP) </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">39,5 </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">μ</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">g / ml (reference values : < 10 ng/ml) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">07/11/2006 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver Ultrasonogram </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 7,9 cm diameter</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">06/02/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Triplex </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation diameter 52,8 mm </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>06/02/2007</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A-Fetoprotein (a-FP)</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">364,8 (reference values : < 7,0 ng/ml) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">07/02/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver Ultrasonic Control 4D </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 3,9 X 3,2 cm diameter</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">09/05/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver Ultrasonic Control 4D </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation </span><span lang="EN-US" style="color: black; font-family: Arial; font-size: 12.5pt;">diameter 21,8 mm </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">09/05/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A - FP </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">22,45 ng / ml (reference values: </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">< 10) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">09/05/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CA 19-9 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 9,16 IU / ml (reference values: <u><</u> </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">39,0 )</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">09/05/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">C.E.A </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 2,77 ng / ml (reference values: </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> < </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">5</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">)</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">18/7/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A-Fetoprotein (AFP) </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">10,9 ng / ml (reference values: 0,0 – 15,0) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">18/7/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CA 19-9 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">6,6 IU / ml (reference values <u>< </u>39,0 )</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">18/7/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CEA</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">2,2 ng / ml (reference values 0,0 – 5,0 ) </span></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">18/7/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Calculating Tomography </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 3<b> </b>cm<b> </b>maximum diameter </span></div>
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<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">10/10/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">AFP </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">18,4 ng / ml (reference values: 0 - 8,1) </span></div>
</td></tr>
<tr><td height="23" style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">10/10/2007 </span></div>
</td><td height="23" style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CA 19.9 </span></div>
</td><td height="23" style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 4,9 U / ml (reference values: 0 - 37 )</span></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">10/10/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CEA</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 1,32 ng / ml (reference values: < 5 )</span></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt; font-weight: 700;">12/10/2007 </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Ultrasonic Control 4D </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 2,9 mm<b> </b>maximum diameter and volume 9,4 ml </span></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>16/11/2007</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Ultrasonogram of the upper abdomen</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 4,75 X 2,19 cm </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>02/01/2008</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Calculating Tomography</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation 20 mm maximum diameter </span></div>
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<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>07/01/2008</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Ultrasonic Control 4D</span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Liver tissue formation of maximum diameter 2,9 mm and volume 9,4 ml</span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>07/01/2008</b> </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">NF – kB </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 3,144 ( reference value < 18,368) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<br /></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<br /></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<b><span lang="el" style="font-family: Arial; font-size: 12.5pt;">16/</span><span style="font-family: Arial; font-size: 12.5pt;">0</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">1/2008</span></b></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">AFP </span></div>
</td><td style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm; width: 270.7pt;" valign="top" width="361"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">54</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">,</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">2</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> ng / ml (reference values: </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">0 - 8,1</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">) </span></div>
</td></tr>
<tr><td style="border-bottom: windowtext 1pt solid; border-left: windowtext 1pt solid; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<b><span lang="el" style="font-family: Arial; font-size: 12.5pt;">16/</span><span style="font-family: Arial; font-size: 12.5pt;">0</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">1/2008</span></b></div>
</td><td height="23" style="border-bottom: windowtext 1pt solid; border-left: medium none; border-right: windowtext 1pt solid; border-top: medium none; padding-bottom: 0cm; padding-left: 5.4pt; padding-right: 5.4pt; padding-top: 0cm;" valign="top"><div class="MsoNormal">
<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CA 19.9 </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 4,</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">1</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> U / ml (reference values: </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">0 - </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">3</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">7</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> )</span></div>
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<b><span lang="el" style="font-family: Arial; font-size: 12.5pt;">16/</span><span style="font-family: Arial; font-size: 12.5pt;">0</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">1/2008</span></b></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">CEA</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> 1,</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">06</span><span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> ng / ml (reference values: </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"> < </span><span lang="el" style="font-family: Arial; font-size: 12.5pt;">5</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">)</span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;"><b>23/01/2008</b> </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A-</span><span style="font-family: Arial; font-size: 12.5pt;">F</span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">etoprotein (AFP) </span></div>
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<span lang="el" style="font-family: Arial; font-size: 12.5pt;"> </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">56,0 ng / ml (reference values: 0,0 – 15,0) </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">Comments :</span></div>
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<span style="font-family: Arial; font-size: 12.5pt;"><br />Liver tissue formation - as measured by calculating tomography - has been reduced from a 8 cm diameter to a 2 cm maximum diameter within 17 months, that is from August 2006 to January 2008. </span></div>
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<span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">A - Fetoprotein has been reduced from 60500,0 ng/ml to </span><span lang="EN-US" style="font-family: Arial; font-size: 12.5pt;">56,0 ng/ml within 16 months, that is from September 2006 to January 2008 <br /> </span></div>
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papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-76729691363837588082011-09-30T07:12:00.000-07:002011-09-30T07:16:57.474-07:00Reports on cancer with pulses similar to PAPIMI<div dir="ltr" style="text-align: left;" trbidi="on">
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<div id="pageheading">
Zap</div>
By: <span class="by"><span class="name">Karl H. Schoenbach</span>,<span class="name"> Richard Nuccitelli</span>, and<span class="name"> Stephen J. Beebe</span></span><br />
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40 Thousand volts, four thousand amperes, and over one hundred million watts squeezed into a cubic centimeter. You’d think that would be enough to vaporize just about anything, and it certainly doesn’t seem like the kind of electricity you’d want to apply to your body. But if our research continues to succeed as it has, years from now we’ll be asking some cancer patients to do just that. And it might just save their lives.<br />
The trick is to apply that gargantuan jolt for only a few billionths of a second. That’s so brief a time that the energy delivered is a mere 1.6 joules per cubic centimeter—barely enough to warm a thimbleful of water by a third of a degree Celsius. But these powerful, ultrashort voltage pulses do something nothing else can—harmlessly slip past a cell’s exterior to shock the vital structures within.<br />
The effects of such pulses of power on living tissue are profound and varied. Malignant tumors—in mice, at least—can be completely wiped out, even by significantly lower power levels; new genes can be efficiently inserted into living cells in the hope of correcting genetic defects; and immune-system cells can be marshaled to fight off invading microbes.<br />
A new field of research, bioelectrics, is emerging to study these effects, as well as the naturally occurring electric fields in biological systems. Bioelectrics relies on a curious pairing of disciplines that until now have had almost nothing to do with each other: high-voltage engineering and cell biology. In particular, the new field depends on advanced pulsed power technology. That’s the ability to switch on and off thousands of amperes of current and just as many volts in mere nanoseconds (the kind of parameters needed to detonate nuclear bombs, it so happens).<br />
The use of high voltages and currents to manipulate structures inside cells is barely five years old, but it is a fast-growing international research endeavor. The largest R&D program at the moment is being supported by the U.S. Air Force Office of Scientific Research, in Arlington, Va. That program supports work at a new center established jointly by Old Dominion University and Eastern Virginia Medical School, where we authors are working, as well as at several other institutions in the United States, including the Massachusetts Institute of Technology, the University of Texas Health Science Center, the University of Wisconsin–Madison, and Washington University. Progress in this program has already sparked interest and some excellent science at academic institutions in Japan, China, and the state of California. And more institutions, notably in the UK, France, and the state of Missouri, are planning bioelectrics research.<br />
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It’s easy to see the attractions for biologists and for engineers. For biologists, it’s the potential scientific payoff: these strong but exceedingly brief electric fields act as a kind of electrical probe, letting scientists prod key structures inside cells—making the cells expel certain vital chemicals or begin the production of others—with the aim of understanding basic biological processes. For engineers, it’s the opportunity to forge an important new application of pulsed power technology, which even 10 years ago was seldom used outside the military.<br />
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The most promising and practical result so far has been our recent discovery that certain pulsed electric fields can wipe out skin tumors in mice. Melanoma, the skin cancer we’ve worked with, is an extremely aggressive disease that kills about 8000 people a year in the United States alone. A few hundred pulses totaling just 120 microseconds of treatment shrank tumors in mice by 90 percent. A second treatment, days later, destroyed the tumors completely.<br />
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Biomedical science is, of course, littered with cancer cures that work in mice but fail or are impractical in humans. And it will be many years before we know if bioelectrics will even be worth testing in humans. Nevertheless, even at this early stage, bioelectrics seems to offer a totally new therapeutic avenue—one that could lead to a therapy free of the debilitating side effects of chemotherapy drugs and the tissue damage of radiation.<br />
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<span class="bold">To understand what happens</span> when a cell is hit with tens of thousands of volts, and why it may help cure disease, you have to know something about cells themselves. At its simplest, a cell is a pocket of water containing a bunch of small functional units called organelles, which are bounded by oily membranes. These organelles are the cell’s version of internal organs: they perform the functions that keep the cell alive, just as the brain, kidneys, and lungs, among other organs, keep the body alive.<br />
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Cells do the things they need to do—contract if they are muscle cells, sense light if they are retinal cells, transport oxygen if they are blood cells—because they produce proteins with specialized functions. The creation of proteins begins in the nucleus, the cell’s most prominent and arguably most important organelle. It houses the cell’s fantastically complex genetic programming apparatus, which lets the cell repair itself and tells it how and when to reproduce, what to do when it detects a particular hormone, and how and when to die. Errors in these genetic programs go to the heart of most of the diseases suffered by humankind. These errors can predispose a person to heart disease, cancer, schizophrenia, and countless other maladies.<br />
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The programs are written into your genetic code. This code exists physically as a set of 23 pairs of chromosomes that reside in the nucleus. Each chromosome is a rod-shaped or threadlike structure of deoxyribonucleic acid, or DNA, made up of a sequence of four chemical building blocks. The sequence of these building blocks—there are tens of millions of them on a single chromosome—is the code, and the “words” of this code are genes. In effect, genes are segments of a chromosome’s DNA. They are groups of many thousands of building blocks that encode a specific protein, with each chromosome containing thousands of genes.<br />
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These genes are the blueprints for the proteins that determine whether you have brown or blue eyes, whether your hair is straight or curly, whether you are tall or short, and whether you are likely ever to suffer from depression, schizophrenia, or cancer. That’s why gaining control of what goes on inside the nucleus—which genetic programs are turned on or off and when—has been a primary goal in biomedical science practically since the discovery of the structure of DNA about 50 years ago. It is the object of the long-standing, multimillion-dollar research endeavor called gene therapy, which after decades of work in some of the world’s foremost laboratories has had mixed results.<br />
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Basically, our work with nanoseconds-long, high-voltage pulses offers a way to gain access to the cell’s organelles, including its nucleus—something that has historically bedeviled biomedical scientists. Remember that the cell and its organelles are bound by membranes. The main component of these 5-nanometer-thick boundaries is called a phospholipid bilayer. It is an oily barrier that blocks the flow of water and ions and therefore also blocks the flow of electric current.<br />
However, the membranes are also studded with proteins, some of which form nanometer-scale channels designed to allow specific ions to flow in a direction useful to the cell. In a way, a cell’s membranes are like leaky capacitors. (Some, such as the one surrounding the nucleus, leak more than others.) To extend this analogy, the briny fluid within the membranes, the cytosol, is conductive and can be thought of as a resistor [see illustration, “Cellular Circuit”].</div>
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Now consider what happens when you apply a pulse to the cell. In general, there are four important characteristics that determine the precise effects. These are how fast the pulse comes on, or its rise time; how long the pulse lasts; how many pulses there are; and, of course, how great the peak voltage is. Different values for each produce a range of effects, but it’s a very fast rise time that makes it possible to electrically manipulate organelles.<br />
To see why rise time is critical, imagine a long voltage pulse applied to the cell that comes on rather slowly, in milliseconds, say. This slow-rising pulse will set up an electric field across the cell membrane. In response, ions dissolved in the cell’s cytosol will stream to the cell membrane, charging it up to counteract the applied field. Because the voltage is rising rather slowly, the ions have enough time to accumulate at the cell membrane and cancel out the electric field, thereby shielding internal structures, such as the nucleus, from the voltage.<br />
Now, as with any capacitor, if too much charge gathers at the cell membrane, the electric field there breaks the membrane down. In a cell, this means large holes, or pores, form in the membrane and allow ions to pour across, short-circuiting the cell. This effect is called electroporation, appropriately enough, and it is generally reversible and even useful. Scientists hoping to kill tumors more efficiently, use electroporation experimentally, for instance, to increase the amount of chemotherapy drugs that tumors take up. In fact, San Diego–based Inovio Biomedical Corp. is in the late stages of clinical tests on such a cancer treatment for tumors of the head and neck.<br />
To manipulate a cell’s internal structures, we want instead to generate a strong electric field inside the cell, and do it before too much charge has accumulated at the cell membrane and turned it into Swiss cheese. Take the case of a brief pulse with a fast rise time, reaching its full force in a matter of nanoseconds. With so brief a rise time, not enough ions will have time to reach the cell membrane to counteract the sudden electric field, so the nucleus and other organelles will feel the field’s full effect.<br />
For pulses with a fast rise time, then, the electric field charges up the membranes of both the cell and its organelles. Generally, the cell’s plasma membrane doesn’t fully charge to the point where large pores form in it until it’s been exposed to at least a microsecond and typically tens of microseconds of voltage. Because the organelles are much smaller than the cell itself, however, they reach their maximum charge much more quickly. Ending the pulse after the organelles are charged up, within a few hundred nanoseconds but before large pores appear in the cell’s own membrane, lets you focus the electric field’s effects on the organelles, such as the nucleus, while leaving the cell membrane relatively untouched. That, in turn, lets you do the complex and varied things medical science is interested in, such as killing tumor cells or triggering an immune system response.<br />
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<span class="bold">This new ability</span> to electrically tweak a cell’s insides would not exist without pulsed power technology: generating, measuring, and using extremely high-power electric pulses. Developed initially to power radar in World War II, pulsed power technology now drives X-ray imagers, particle accelerators, and nuclear weapons, to name a few applications.<br />
The kinds of pulses that work best in bioelectrics are simple rectangular waves. There are a few ways to make such a pulse. The simplest is to discharge a capacitor. Provided that the time it takes the capacitor to discharge is long in comparison to the length of the pulse, you get a roughly rectangular pulse. The problem is that the pulse length is determined by the closing and opening of a switch. And no high-voltage mechanical switch can open and close in the few nanoseconds we need.<br />
Certain types of transistors can do the trick, but they can switch only 1 kilovolt or less, and we usually need 10 kilovolts or more. Switches that can handle that kind of voltage can reliably close in just nanoseconds, but they can’t open so quickly.<br />
What’s needed is a way to separate the length of the pulse from the speed of the switch. A transmission line pulse generator does just that. In electric power, transmission lines are generally paired conductors, such as coaxial cables, that are long in comparison to the wavelength of the signal they carry. In particular, we make use of transmission line generators in a Blumlein configuration, named for the British stereo recording and radar pioneer Alan Blumlein.<br />
Picture two long rectangular conductors sandwiching a thin layer of insulation [see illustration, “<a href="http://www.spectrum.ieee.org/images/aug06/images/zapf2.pdf">Power Pulse</a>”]. One conductor is divided into two pieces of equal length, and the load—in our case, a small tube of cells or a patch of tumor-riddled skin—is placed between them. The other conductor is charged up because it’s connected at one end to a high voltage. And the bisected conductor is grounded at the same end.<br />
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<span class="bold">A Blumlein generator produces brief high-voltage pulses when electromagnetic waves change polarity and collide.</span><br />
Closing a switch connects the two conductors, discharging the device and setting up waves of voltage that rocket along it [see bioelectric researcher Juergen F. Kolb's animated clip of the waves in the online version of this article at<a href="http://www.spectrum.ieee.org/blumlein">http://www.spectrum.ieee.org/blumlein</a>]. These waves travel in a way not unlike a wave that you’d set up on a length of rope by holding one end and snapping it.<br />
When the switch closes, waves travel both toward and away from the load. For those initially traveling toward the load, some portion reflects off it, and the rest transmits right across it. For those waves traveling away from the load—including the portions that have now transmitted across—what happens depends on which end of the device they encounter.<br />
Taking the rope analogy again, note that if you send a wave down a rope, the wave will reflect off the end and head back toward you. If the end is hanging loose, the reflection will be of the same phase as the initial wave. That is, if the voltage change was positive, the reflection will be, too. But secure the loose end and the wave will invert when it reflects. The unsecured rope is analogous to the end of the transmission line opposite the switch. The secured end, on the other hand, is like the end at the closed switch.<br />
The voltage pulse comes about when the inverted reflection and the noninverted reflection crash into each other at the load. The pulse ends when the trailing edge of each wave has completed its trip down the transmission line to the load. Therefore, it is not necessary to open a switch to terminate the pulse; it simply ends abruptly when there is no energy left in the line. What’s more, you can easily adjust the duration of the pulse by either adding or subtracting length from the transmission line.</div>
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<span class="bold">So what happens</span> to a cell when you zap its innards with so much power? We’re still working out the biological details, but experiments using cancer cells suspended in liquid or even growing as tumors in mice have yielded a good deal of insight.<br />
In our most recently reported experiments, we injected melanoma cancer cells under the skin of 120 mice and allowed tumors to form [see photo, “Diminished”]. We then used a Blumlein pulse generator to subject the tumors to electric field pulses 300 nanoseconds long—too short to cause classical electroporation—that reached 90 percent of their peak of 40 kilovolts per centimeter in just 30 ns. We hit the tumors with a total of 400 pulses, one every other second. Over the course of two weeks, the tumors shrank by 90 percent. Then they began to grow again. But in a few experiments, we subjected the tumors to subsequent sets of pulses, and they were destroyed completely and did not grow back.<br />
We believe our ultrashort electric pulses killed the tumor cells by kick-starting a cellular phenomenon called apoptosis, but proving that theory beyond a doubt is difficult. Apoptosis is also called cell suicide or programmed cell death. In apoptosis the cell disassembles itself in an orderly fashion in minutes or hours, leaving behind only fragments useful as recycling material for the body. It is a process that allows the removal of cells that are no longer needed by the organism or of cells that pose a threat to it. As part of the apoptosis system, cells can sense if they are too badly damaged to reproduce correctly. Almost by definition, in cancers, the apoptosis system is off-line, allowing a dangerously aberrant cell not only to survive but also to multiply.<br />
We saw two nearly immediate effects of the pulses in the mouse tumors that could indicate apoptosis. First, within just a few minutes, the tumor cell nuclei had shrunk to half their original sizes, suggesting that the electric field had either directly or indirectly damaged the cell’s DNA.<br />
Also, separate experiments done on cells in a liquid suspension showed that similar pulses resulted in broken DNA and that genetic programs involved in DNA repair became more active in the pulses’ aftermath. DNA damage can trigger apoptosis, but such damage also occurs during apoptosis. However, a classic experiment to prove that apoptosis is in progress, measuring the amount of a chemical called caspase in cells, showed no change and no apoptosis.<br />
We think that’s because of the second immediate effect we observed: within minutes of treatment, blood stopped flowing to the tumor. It takes energy for a cell to kill itself—in other words, apoptosis can’t happen without a steady supply of nutrients and oxygen from the blood. Though we don’t know the exact reason blood stops flowing, stopping the flow is clearly helpful in destroying tumors. Malignant tumors can grow to dangerous proportions only because they have the ability to trick the body into growing new blood vessels to feed them. Developing drugs to starve tumors by disrupting their blood supply and their ability to build a new supply is a major goal of many pharmaceutical firms. And it appears that disrupting the blood supply is something that nanoseconds-long pulsed electric fields can do.<br />
A key measure of how useful a cancer treatment might be is if it is more harmful to tumors than to normal tissue. When we shocked vials containing both cancer cells and normal cells, the pulses killed only the cancer cells. However, in the mouse experiments, our pulses did some damage to healthy skin surrounding the mouse tumors. But this blackening was temporary, and within a couple of weeks, the skin had healed. Minor tissue damage is common in cancer therapies. In fact, most treatments, such as chemotherapy, are damaging to tumors and healthy tissue alike, but they rely on the fact that healthy tissue has working genetic programs that allow it to survive the chemical attack and tumors do not.<br />
We are probably years away from performing a similar test of ultrashort high-power pulses on human cancer patients. But even if those tests are successful, there will be many hurdles to overcome for nanosecond pulsed electric fields to become a viable treatment in the clinic. For one thing, we must be able to deliver gigawatts of power accurately to sites deep within the body—not just at the skin surface where we can pinch the tumor between two parallel plates or poke it with pin electrodes. And we must be able to do so with little or no harm to the surrounding healthy tissue.<br />
So this summer we are working with antenna expert Carl E. Baum, at the University of New Mexico, in Albuquerque, to build a device to let us beam the pulses at cells deeper inside the body. When pressed against the skin, such a pulse generator’s half-ellipsoid antenna should focus an electric field pulse to a small volume several centimeters inside the body. The antenna is only at the modeling stage, but using our existing laboratory equipment we have begun to examine what sorts of pulses it would create and what those pulses would do to living cells.<br />
For the time being, though, and notwithstanding the fact that we’ve made a lot of progress observing the effect of this high-voltage treatment on tumors in mice, we know far too little about it now to move on to experiments in humans. It’s important to keep in mind that the majority of new therapies that show promise in the lab never develop into approved treatments. We hope nanosecond pulses will, but the road ahead will be twisty and difficult.</div>
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<span class="bold">Cancer cells</span> are just one target of ultrashort pulsed electric fields. By lowering the power and altering their target, for example, we can also use the pulses in gene therapy. For instance, in proof-of-principle experiments, we used the pulses to insert new genes into chromosomes in the nuclei of cells—one of the key challenges of gene therapy.<br />
For various reasons, the enormous potential of gene therapy has largely eluded medical researchers. Basically, the techniques have proven difficult for physicians to execute and dangerous for patients subjected to them. A prominent example of gene therapy in humans was a trial in Europe in the 1990s to treat severe combined immune deficiency syndrome. Commonly called “bubble boy” syndrome, the disease is caused by an inherited defect in a single gene, which cripples the body’s defense against infection.<br />
To combat the disease, doctors introduced a corrected copy of the gene into the nuclei of the children’s immune-cell-generating tissue. Encouragingly, the therapy defeated the disease, but unfortunately, three of the first 11 patients developed leukemia, caused by the way the new gene inserted itself into their existing DNA. Despite the setbacks, medical scientists have not given up on gene therapy for bubble-boy syndrome and are also trying it out for nerve damage from diabetes, heart failure, hemophilia, and a host of other diseases.<br />
Another reason to insert new genes into people is to immunize them against a particular disease. Ordinary vaccines provide immunity because they are made up of crippled or dead versions of a disease-causing microbe. Exposure to a neutered version of the microbe enables our immune systems to recognize the chemical characteristics of the weakened microbe and to mount a fast, effective defense against the real version. However, the vaccine must be refrigerated, and if the microbe is not weakened enough—and this only very rarely occurs—it can cause rather than protect against the disease.<br />
Partly because of these drawbacks, researchers have become intrigued with the idea of injecting a person with the DNA that codes for one of the infectious bug’s proteins. Some of the person’s own cells take up the DNA, produce the protein, and trigger the immune system to learn to recognize and defend against any microbe carrying that protein.<br />
Among the chief technical difficulties with these DNA vaccines, as well as with gene therapies, is getting the DNA into cells. Simply injecting a dollop of DNA into someone is not good enough, because the cell membrane is such a strong barrier against DNA. One popular solution is to actually genetically engineer the DNA into a virus. Viruses infect us by “sneaking” their genetic material through the cell membrane and tricking the cell into copying it. So scientists have sought to include the DNA they want into harmless viruses, with which they then infect the patient in the hopes that the virus will deliver the new gene to the place it needs to go.<br />
The problem is that the virus can stitch the new gene into a bad spot in the cell’s own DNA, disrupting an important chemical program and causing disease, as happened when the immune-deficient children developed leukemia. Or the virus itself can cause a runaway immune system reaction that can kill the patient, as seems to have happened in a gene therapy trial several years ago at the University of Pennsylvania, in Philadelphia.<br />
Pulsed electricity may offer a safer solution. First we can use strong, but rather long-lasting, electric fields to induce electroporation, the state we mentioned earlier in which the cell’s outer membrane temporarily becomes porous. This works, to a point, because although the new DNA can now enter the cell, it must still get past the nucleus’s membrane for the cell to decode it.<br />
Because the ultrashort pulses we’ve worked with appear to affect subcellular membranes, such as the double membrane that bounds the nucleus, we figured they might help genes make it through that last step of their journey by opening pores in the nuclear membrane. As a test, we tried to insert a certain gene from a jellyfish into bone marrow cells in a test tube. If this gene makes it into the nucleus and is decoded, it produces a protein that glows green.<br />
By itself, electroporation improved the amount of the gene that was taken into the cells’ nuclei by 260 percent, as measured by the number of cells glowing and the strength of the green glow. But following electroporation with a nanoseconds-long pulse aimed at opening the cells’ nuclei increased gene uptake by a whopping 900 percent—potentially enough to improve the efficiency and safety of gene therapies or DNA vaccinations.<br />
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<span class="bold">The list of effects </span>that scientists have achieved using nanoseconds-long pulses is growing rapidly, though their actual use as a medical treatment is still years away. For example, brief pulses cause platelets, cellular fragments in the blood, to begin the complicated cascade of steps needed to form clots. Though the experiments were performed in a test tube rather than on a human being, we hope the effect might one day be used in healing wounds.<br />
In other research, E. Stephen Buescher, a professor of pediatrics at Eastern Virginia Medical School, did a fascinating set of experiments with white blood cells that also might ultimately help heal wounds. In it, he observed the effect of ultrashort pulses on the release of calcium inside cells from internal stores. Calcium acts as a kind of signal transducer in many cells, translating an external signal such as a hormone into some cellular action, such as manufacturing a protein.<br />
In a type of white blood cell whose purpose is to seek out foreign material and digest it, for example, the release of calcium allows the cell to follow an invader’s chemical trail. When Buescher subjected these cells, called leukocytes, to nanoseconds-long, 12-kV/cm electric fields, the cells immediately, but briefly, spilled calcium from their internal stores into their own cytosol. In experiments where the cells were actively crawling over a microscope slide, hot on the simulated trail of an invader, pulsing stopped them in their tracks and then sent them marching off in the direction of the electric field. One day doctors might use such an effect to recruit immune cells to the site of an infection.<br />
The list of cells and the effects of pulsed power on them goes on and will only get longer as more laboratories begin work in bioelectrics. Scientists at Kumamoto University, in Japan, for example, are studying the subcellular effects of high-power RF pulses. Those at Karlsruhe University, in Germany, are testing nanopulses for killing bacteria. And researchers at the University of Southern California are studying how the pulses cause dying cells to signal other cells to consume them. Whether or not pulsed power becomes a cancer treatment, a gene therapy technology, or an infection fighter, ultrashort electric fields have already proved a powerful research tool. And the mark they ultimately make on medicine may be in allowing scientists unprecedented access to the internal workings of cells.<br />
Still, we hope for more practical—and potentially lucrative—possibilities. While treatments for cancer and genetic diseases would be revolutionary, somewhat more prosaic applications are in the offing. We at Old Dominion University have recently used nanosecond pulsed electric fields to destroy fat cells. Think of it as electric liposuction. Hey, if it helps pay for the research needed to fight dread diseases, we’re all for it.</div>
<h2>
About the Authors</h2>
<div class="bio">
Karl H. Schoenbach, an IEEE Fellow, holds the Frank Batten Endowed Chair in Bioelectric Engineering at Old Dominion University, in Norfolk, Va. There he directs the Frank Reidy Research Center for Bioelectrics.<br />
Richard Nuccitelli is a biophysicist at Frank Reidy who has studied the role of ion currents and ion concentration changes in the regulation of cell physiology for 30 years. He was the lead investigator on the melanoma project.<br />
Steven J. Beebe is a faculty member in the department of physiological sciences and pediatrics at Eastern Virginia Medical School, in Norfolk, and is on the staff at Frank Reidy. He has studied mechanisms for signal transduction and apoptosis regulation for decades.<br />
<span class="italic">Acknowledgments</span><br />
<span class="italic">The authors would like to thank Peter F. Blackmore, E. Stephen Buescher, Ravindra P. Joshi, Juergen F. Kolb, and R. James Swanson.</span></div>
<h2>
To Probe Further</h2>
<span class="italic">Proceedings of the IEEE</span> devoted its July 2004 issue to pulsed power technology and its applications. The issue includes a more detailed look at bioelectrics: “Ultrashort Electrical Pulses Open a New Gateway Into Biological Cells,” by Karl H. Schoenbach et al., pp. 1122–37.<br />
For more on the effects of nanosecond pulses on cell biology, see “Nanosecond Pulsed Electric Fields Modulate Cell Function Through Intracellular Signal Transduction Mechanisms,” by Stephen J. Beebe et al., <span class="italic">Physiological Measurements</span>, Vol. 25, 2004, pp. 1077–93.<br />
For the latest on the authors’ experiments on melanoma, see “Nanosecond Pulsed Electric Fields Cause Melanomas to Self-destruct,” by Richard Nuccitelli et al.,<span class="italic">Biochemical and Biophysical Research Communications</span>, 5 May 2006, pp. 351–60.<br />
<span class="captiontitle"><br />Cellular Circuit</span>: A cell can be thought of as a circuit made up of capacitors and resistors. Its membrane and those of its organelles, such as the nucleus, act like capacitors. The briny liquid encased within the membranes, the cytosol and nucleoplasm, is conductive and so can be modeled as resistors.<br />
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<span class="captiontitle"><br />Diminished</span>: A skin tumor in a mouse before [top] and 16 days after [bottom] treatmentwith nanoseconds-long pulses of voltage.</div>
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Images: Frank Reidy Research Center for Bioelectrics</div>
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Source <a href="http://www.papimi.gr/">www.papimi.gr</a> </div>
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<a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com</a></div>
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papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-12931910355979287322011-09-30T06:31:00.000-07:002011-09-30T06:37:51.872-07:00<div dir="ltr" style="text-align: left;" trbidi="on">
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<a href="http://papimi.gr/MRI_scan.htm"><i><b>UNDISPUTABLE SCIENTIFIC EVIDENCE ABOUT THE NON CHEMICALLY ENERGIZED PAPIMI WATER<span style="font-family: 'Arial Black'; font-size: large;"> click here to see relevant pictures</span></b></i></a></div>
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<span style="font-size: large;"><i><b>NEW BREAKTHROUGH FACTS:</b></i><br />The scientific objectiveness of the energized PAPIMI water can be shown by MRI Magnetic Resonance Imaging. MRI is the most advanced diagnostic imaging technique in medicine, used widely today.</span><br />
<span style="font-size: large;">With the following experiment:<br />Seven identical sealed bottles with the same distilled water are prepared, the 2 of the 7 bottles are exposed 20 minutes with the PAPIMI probe. Then, the same thing is repeated with the other 2 bottles, but exposure time now is 10 minutes. 3 bottle are left without any exposure.</span><br />
<span style="font-size: large;">Then all 7 bottles, about six hours later, are brought to an MRI Center, placed simultaneously and one next to the other in the MRI chamber to be photographed.<br /><br />Results:</span><br />
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<span style="font-size: large;">All 3 Bottles without exposure at all comes out dark</span><br />
<span style="font-size: large;">All 2 Bottles exposed 20 minutes comes out bright</span><br />
<span style="font-size: large;">All 2 Bottle exposed 10 minutes comes out </span><b><span style="font-size: x-large;"> </span></b><span style="font-size: large;">half bright</span><br />
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<br />
THE SECRETS OF PAPIMI WATER<br />
<b><span style="color: red; font-size: x-large;"><br /></span></b><br />
<b><span style="color: red; font-size: x-large;">IN ALL CASES<br />DRINK AS MUCH AS YOU CAN PAPIMI ENERGIZED WATER<br />energize your body with papimi energized water and feel the power</span></b></div>
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<span style="font-size: x-large;"><b>NEW</b></span><b><span style="font-size: x-large;"> PAPPAS' SCIENTIFIC BREAKTHROUGH PROOF FOR NON CHEMICAL PROPERTIES OF WATER:<br /><br />"SOME WATER PROPERTIES ARE NOT DETERMINED BY ITS CHEMICAL COMPOSITION BUT ALSO DEPEND ON ITS PREVIOUS MAGNETIC TREATMENT THAT DOES NOT ALTER ITS CHEMICAL COMPOSITION"</span></b><br />
<span style="font-size: x-large;">THE HYPOTHESIS OF CRYSTAL WATER</span><span style="font-size: medium;"><b> <a eudora="autourl" href="http://www.theresedilor.com/esther.html">http://www.theresedilor.com/esther.html</a></b></span><span style="font-size: large;"> by Dr. Esther Del Rio.</span><span style="font-size: x-large;"></span><br />
<span style="font-size: large;">Liquid water can form icosahedral water clusters :</span><span style="font-size: medium;"> </span><a eudora="autourl" href="http://www.lsbu.ac.uk/water/abstrct.html"><span style="font-size: medium;">http://www.lsbu.ac.uk/water/abstrct.html</span></a><br />
<span style="font-size: medium;">Water effects on health : References <a href="http://www.papimi.gr/nero.htm">www.papimi.gr/nero.htm</a></span><br />
<b><span style="font-size: x-large;"><br />TREATING WATER WITH PAPIMI</span></b><br />
<span style="font-size: large;">There seems to be two ways of transferring the benefits of papimi.</span><br />
<span style="font-size: large;">The first way is to apply the probe over the object one wants to transfer the benefit.</span><br />
<span style="font-size: large;">The second way is to treat the water that will be watering the plants. </span><b><a href="http://www.papimi.gr/plantpic.htm"><span style="font-size: medium;">http://www.papimi.gr/plantpic.htm</span></a></b><br />
<table border="1" id="table1"><tbody>
<tr><td><span style="font-size: medium;"><br /> </span><span style="font-size: 22pt; font-weight: 700;">See among the numerous experiments, the substantial difference in growth with and without papimi activated water.</span><br />
<a href="http://papimi.gr/treat10a.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="199" src="http://papimi.gr/treat10a.jpg" width="89" /></a><span style="font-size: large;"><b>The PAPIMI activated water.</b> <b> was given to the pot with white label with beans seeds</b> </span><br />
<span style="font-size: large;"><b>After 9 days six seeds have developed considerably.</b></span><br />
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<a href="http://papimi.gr/treat10b.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"></a><a href="http://papimi.gr/untreat10b.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="199" src="http://papimi.gr/untreat10b.jpg" width="142" /></a><a href="http://papimi.gr/untreat10a.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="178" src="http://papimi.gr/untreat10a.jpg" width="92" /></a><b> </b><span style="font-size: large;"><b>Normal water</b>. <b> was given to the next pot with the same number of beans seeds</b> </span><br />
<span style="font-size: large;"><b>After 9 days one seed is just underdeveloped.<br /> </b></span><br />
<span style="font-size: large;"><b>This experiment was repeated by us very very many times and the Agricultural University of Athens (AUA) with hundreds of plants and always with the same results. See confirming letter of AUA below.</b></span><br />
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<a href="http://papimi.gr/Efthimiadis_2003.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="358" src="http://papimi.gr/Efthimiadis_2003.jpg" width="263" /></a></div>
<a href="http://papimi.gr/treat10b.jpg" imageanchor="1" style="clear: left; float: left; margin-bottom: 1em; margin-right: 1em;"><img border="0" height="200" src="http://papimi.gr/treat10b.jpg" width="143" /></a> <i><b><a href="http://papimi.gr/Efthimiadis_2003.jpg">clicktoenlarge</a> <a href="http://papimi.gr/Efthimiadis_2003eng.jpg"><img border="0" height="374" src="http://papimi.gr/Efthimiadis_2003eng.jpg" width="290" />clcktoenlarge </a> </b></i><br />
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<b><a href="http://www.papimi.gr/plantpic.htm">COMPARISON RESULTS :</a></b></div>
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<b><a href="http://www.papimi.gr/plantpic.htm">Exposed Plants with twin Plants Non Exposed for about 10 minutes exposures every other day. http://www.papimi.gr/plantpic.htm</a></b></div>
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<span style="font-size: large;"><img border="0" height="199" src="http://papimi.gr/plants23.jpg" width="294" /><br /><br /> </span></div>
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<b><span style="font-size: large;">Also, see the typical difference between the plant (peas) growth given activated water (white label on the pot), and the similar plant given normal water, after 14 days</span></b><i><b><span style="font-family: Arial; font-size: x-large;"><a href="http://whos.amung.us/stats/i5tj56aji19t/"><span style="text-decoration: none;"><span style="color: white;"><img border="0" height="2" src="http://whos.amung.us/widget/i5tj56aji19t.png" title="Click to see how many people are online" width="5" /></span></span></a></span></b></i></div>
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<span style="font-size: large;">By treating water in shielded plastic bottles as shown, at then to apply or supply the water, if possible, to the object. Hundreds of experiments like this at our Laboratories as well at the Agricultural University of Athens, has shown that something is indeed stored in the water that provides similar or better results as in the first way, by drinking the treated water, by watering plants, etc.<br /><br />PAPIMI treated water seems to act as the so called crystal water. Analysis and comparisons of the PAPIMI WATER and CRYSTAL WATER </span><span style="font-size: medium;"><b><a eudora="autourl" href="http://www.theresedilor.com/esther.html">http://www.theresedilor.com/esther.html</a></b></span><span style="font-size: large;"> by Dr. Esther Del Rio is on the way and we shall reports the results here as soon as they are conclusive.</span><br />
<span style="font-size: large;">What is certain now and here is not all the properties of the water are due to its chemical composition. More beneficial properties seem to be due perhaps to a so called crystalline structure of the water of 37 molecules, which primarily affect biological shaping of plants and animals.<br /><br />FOR EXAMPLE<br /> </span><br />
<span style="font-size: large;">PAPIMI WATER watering plants develops these plants to their maximum height from seeds several times faster.</span><br />
<span style="font-size: large;">PAPIMI WATER seem to enable the eliminations of scars due to wounds, burns, or even marks due to tumor as direct PAPIMI EXPOSURE seem to do.<br /><br />Professor<br />Panos Pappas,<br />PhD Physics.</span><br />
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<span style="font-size: large;"> </span>TREATING AND ENERGIZING<br />
WATER WITH PAPIMI</div>
<img border="0" height="236" src="http://papimi.gr/papimibottle.jpg" width="312" /><br />
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<img border="0" height="254" src="http://papimi.gr/water3.jpg" width="315" /><br />
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<img border="0" height="221" src="http://papimi.gr/water2.jpg" width="313" /><br />
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<span style="font-size: x-large;">USING PAPIMI AND PAPIMI WATER</span><span style="font-size: medium;"><br /></span><span style="font-size: x-large;">SYNERGETICALLY TO ELIMINATE FOOT MARKS<br /> </span><br />
<img border="0" height="224" src="http://papimi.gr/papimiwater1.jpg" width="313" /><br />
<span style="font-size: medium;">Important Notice: A plastic container, a ground and an insulated chair are required as shown, for safety to act independently of the safety leakage controls of papimi device (0.3ma new devices, 3ma older devices).</span><span style="font-size: x-large;"> </span>Otherwise and better, you may use papimi device first and then papimi water, or the other way around, afterwards and separately.<br />
<b><span style="color: red; font-size: x-large;">IN ALL CASES<br />DRINK AS MUCH AS YOU CAN PAPIMI ENERGIZED WATER<br />AND FEEL THE POWER</span></b></div>
papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-16249178923694381252011-09-15T00:43:00.000-07:002011-09-15T00:44:54.523-07:00Treatments for PEMF Devices<div dir="ltr" style="text-align: left;" trbidi="on">
<h3>
<span class="mw-headline" id="Delayed-_and_Non-Union_Fractures">Delayed- and Non-Union Fractures</span></h3>
In 1974 it was demonstrated that a pulsed magnetic field applied across the site of a bone fracture can accelerate the healing process (BASSETT et al., 1974). The mechanism of osteogenesis is not clear, however the use of PEMF therapy as an adjuvant therapy for delayed- and non-union fractures was supported by empirical evidence collected through clinical studies. Whilst PEMF therapy may offer some benefit in the treatment of fractures, the evidence is inconclusive and is insufficient to inform current clinical practice.<sup class="reference" id="cite_ref-16"><a href="http://en.wikipedia.org/wiki/Pulsed_Electromagnetic_Field_Therapy#cite_note-16"></a></sup><br />
PEMF therapy has been suggested to enhance healing of fractures that occur in patients with diseases such as diabetes, vascular insufficiency, and osteoporosis, and those taking medications such as steroids and non-steroidal anti-inflammatory drugs. The exact mechanism for fracture healing is unclear; however, it is thought that PEMF therapy causes biochemical changes at the cellular level to accelerate bone formation.<br />
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<span class="editsection"></span><span class="mw-headline" id="Post-Operative_Pain_and_Edema">Post-Operative Pain and Edema</span></h3>
There are few clinical trials that have demonstrated PEMF therapy as an effective treatment for tissue trauma, particularly in the early stages of inflammation. Electrical stimulation has been shown to significantly increase the probability of bony arthrodesis in spinal fusions. The use of low-energy, time-varying magnetic fields (commonly referred to as pulsed electromagnetic fields or PEMF) has been successful when used adjunctively to fresh fusions and in the case of treating a failed fusion, PEMF bone growth stimulation is a successful method which avoids a revision surger<span class="mw-headline" id="Chronic_pain"> </span><br />
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PEMF may be a novel, safe and effective therapeutic tool for use in at least certain subsets of patients with chronic, nonmalignant pain.<br />
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For more info on PEMF Devices please visit <a href="http://papimiuk.blogspot.com/">http://papimiuk.blogspot.com </a></div>
papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com3tag:blogger.com,1999:blog-1648381221485527825.post-15124871945849511912011-09-14T01:19:00.000-07:002011-09-14T01:19:36.556-07:00What is Pulsed Electromagnetic Field Therapy ?<div dir="ltr" style="text-align: left;" trbidi="on"><br />
<div class="MsoNormal"><b><span lang="EN-GB">Pulsed Electromagnetic Field Therapy (PEMFT)</span></b><span lang="EN-GB">, also called <b>Pulsed Magnetic Therapy</b>, is a reparative technique most commonly used in the field of orthopedics for the treatment of non-union fractures, failed fusions, and congenital </span><span lang="EN-GB">pseudarthrosis</span><span lang="EN-GB">. PEMF uses electrical energy to direct a series of magnetic pulses through injured tissue whereby each magnetic pulse induces a tiny electrical signal that stimulates cellular repair. </span></div><div class="MsoNormal"><br />
</div><div class="MsoNormal"><span lang="EN-GB">Many studies have also demonstrated the effectiveness of PEMF in healing soft-tissue wounds; suppressing inflammatory responses at the cell membrane level to alleviate pain, and increasing range of motion. The value of pulsed electromagnetic field therapy has been shown to cover a wide range of conditions, with well documented trials carried out by hospitals, rheumatologists and physiotherapists.</span></div><div class="MsoNormal"><span lang="EN-GB"><br />
</span><br />
<span lang="EN-GB"> There are several electrical stimulation therapy devices, approved by the FDA, that are widely available to patients for use. These devices provide an additive solution that aid in bone growth and repair.</span><br />
<br />
<span lang="EN-GB">For more info on PEMF Devices please visit : </span><br />
<br />
<span lang="EN-GB">http://papimiuk.blogspot.com</span><br />
<span lang="EN-GB"><br />
</span></div></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-8657135486044744612011-09-08T07:20:00.000-07:002011-09-20T00:42:57.865-07:00History of Pulsed Magnetic Field Therapy (PEMF)<div dir="ltr" style="text-align: left;" trbidi="on">
<b>History of Pulsed <span class="Apple-style-span" style="background-color: white; color: #222222; font-family: Arial, Tahoma, Helvetica, FreeSans, sans-serif; font-size: 13px; line-height: 18px;">Magnetic Field Therapy (</span>PEMF)</b><br />
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The use of pulsed magnetic field therapy (PEMF) in clinical applications dates back over 500 years. In the 15th century, Swiss physician and alchemist Paracelsus used lodestones, or naturally magnetized pieces of the mineral magnetite, to treat conditions such as epilepsy, diarrhea, and hemorrhage. He believed that the ability of magnets to attract iron could be replicated by attracting disease away from the body. In the late 18th century, the Austrian physician Franz Anton Mesmer, who originated the idea of "animal magnetism", described the healing properties of passing magnets over the open veins of patients.<br />
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In the mid-19th century, magnetic ointments produced in New York were introduced as remedies for a whole spectrum of illnesses such as headaches, inflammation of the bowels, burns, fever sores, rheumatism, gout, and toothache.<br />
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Although electricity’s potential to aid bone healing was reported as early as 1841, it was not until the mid-1950s that scientists seriously studied the subject. Fukada’s and Yasuda’s discovery of the electric potential of bone provides evidence of electricity’s effect in promoting osteogenesis (bone growth), particularly in long bone non-unions.During the 1970s, Bassett and his team introduced a new approach for the treatment of delayed fractures, a technique that employed a very specific biphasic low frequency signal to be applied for non-union/delayed fractures.<br />
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The use of electrical stimulation in the lumbosacral region was first attempted by Alan Dwyer of Australia. In 1974, he reported successful initiation of graft incorporation in 11 of 12 fusion patients. Since that time, electrical stimulation has been shown to significantly increase the probability of bony arthrodesis in spinal fusions.<sup class="reference" id="cite_ref-9"></sup><br />
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In 1979 the FDA approved non-invasive devices using pulsed electromagnetic fields designed to stimulate bone growth.In 1991, <b>PEMF Therapy</b> was approved in the US for adjunctive use in the palliative treatment of postoperative pain and edema in superficial soft tissue.<br />
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In 2004, pulsed electromagnetic field system was approved by FDA as an adjunct to cervical fusion surgery in patients at high risk for non-fusion.<br />
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The use of <u>PEMF</u> stimulation has been found to be safe.It has also been proven safe and effective in treatment of delayed union in long bone fractures and patients at a risk of non-union following spinal fusion surgeries<span class="Apple-style-span" style="font-size: x-small;">.</span><br />
<span class="Apple-style-span" style="font-size: x-small;"><br /></span><br />
<span class="Apple-style-span" style="font-size: x-small;">Source </span><a href="http://en.wikipedia.org/wiki/PEMF">http://en.wikipedia.org/wiki/PEMF</a><br />
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For more info on <i>PEMF Therapy</i> and Magnetic Field Therapy visit: <a href="http://www.papimiuk.blogpost.com/">www.papimiuk.blogpost.com</a><br />
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papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-22903881567316946872011-09-08T07:10:00.000-07:002011-09-08T07:25:43.700-07:00How nanopulse technology can kill off cancerous cells<div dir="ltr" style="text-align: left;" trbidi="on">
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<b>Nanopulse Technology</b><br />
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Using very short, very powerful electric shocks, researchers are developing a way to jolt cancer cells into committing suicide, or healthy cells into healing wounds.</div>
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The technique involves blasting cells with nanopulses. These are high-power electrical bolts that last a few billionths of a second. They deliver millions of volts - enough to light up a city, but each burst lasts much less than the blink of an eye.</div>
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Longer shocks blow a cell apart, but researchers have found that the fleeting nanopulses leave the cell membrane unaffected while mixing up its insides. Now they are working out how to vary the timing and intensity of the shocks to make cells behave in specific ways.<br />
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<span style="font-size: small;"><span lang="EN-US"> We would like to state a more consistent theory of cancer that we came up with, <b>based on ten years of experience</b>. The results are fascinating,</span><span lang="EN-US"> </span><span lang="EN-US">obtained after <a href="http://www.papimiuk.blogspot.com/"><b>PAP IMI™</b></a> exposures, and after comparing these results with other theories and methods</span><span lang="EN-US"> </span><span lang="EN-US">. </span></span></div>
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">The first assumption involves the most basic principle of physics, which we have come to realize several years ago in association with cancer. The assumption concerns the physical energy</span><span lang="EN-US"> </span><span lang="EN-US">of the cell. </span></span><br />
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<span style="font-size: small;"><span lang="EN-US">Energy in physics, as in the universe as a whole, is the most fundamental and universal concept of cause and effect. This controls every action in the cosmos, between a donor of the energy [the cause] and a receptor of the energy [the result]. We may say, a biological system with energy transformed from one form to another or given from a donor to a receptor, is a living system. A biological system with active metabolism and energy not given and taken between donors and receptors (without metabolism) is a dead system. We state below an extremely simple and fundamental principle for cancer in relation to the physical energy condition of a cell. </span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><b><i><span lang="EN-US">Cancer</span></i></b><span lang="EN-US"> <b><i>, is a <u>critically low state of energy</u></i></b> <b><i><u> within a cell and with a critically low metabolism</u></i></b> <b><i>, in which the cell is being “trapped” for various reasons. This critically low energy and metabolism state is manifested by a low transmembrane potential (TMP) of 15 mvolts, which causes a “chain</i></b> <b><i>” of specific malfunctions for the cell, and a general state of ischemia (low energy) for the organism</i></b> <b><i>. When a cell is in this particular low energy/metabolism state and has below TMP of 15 mvolts that is responsible for cell metabolism (Nobel Laureate Albert Szent-Gyorgyi, Cone and others). The extremely weak TMP of 15 mvolts cell divides in two identical parts in an attempt to survive in larger numbers as a species. </i></b></span></span></div>
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<span style="font-size: small;"><b><i><span lang="EN-US">Cancer</span></i></b><span lang="EN-US"> <b><i> is also the most general phenomenon of missing cell energy</i></b> <b><i>, low metabolism and division in biological</i></b> <b><i> systems. It is a phenomenon found in all forms of life, i.e., plants, animals and, we may even say, in all living societies such as that of humans, animals, plants, and various micro-organisms</i></b> <b><i>. </i></b></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><b><i><span lang="EN-US">We may suggest that Cell Cloning, Meristomatic Culturing for plants and Cancer, all have the same starting point in common for cell proliferation, that is metabolic stress, or poor nutrition, long known for cell cloning and meristomatic culturing for plants.</span></i></b></span><br />
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<span style="font-size: small;"><span lang="EN-GB"></span></span><span lang="EN-US">We demonstrate the above, with a common example taken from agriculture, which is known to most farmers: Let us suppose that we have two plants</span><span lang="EN-US"> </span><span lang="EN-US">which we water</span><span lang="EN-US"> </span><span lang="EN-US"> every day. The plants stay healthy, but as a result do not produce flowers or seeds, which would lead to reproduction of the plant. If we deprive one of the plants of its nutrition by halting the water supply, as a result you will find the plant in a state of “stress”. This plant will then produce flowers and seeds in order to multiply and thus survive as a species. This result is due to an “instinct” or “survival program” deeply encoded in its DNA by its creator. This is a general phenomenon of reproduction, known for almost all plants</span><span lang="EN-US"> </span>. <span style="font-size: small;"><span lang="EN-US"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">The same holds true for advanced organisms which may secure food fairly easier versus a primitive one, which strives every day for food. Indeed a primitive organism is in a continuous state of stress while finding food and energy. In order to counter this and overtake its daily battle for food and survival as a species, it multiplies very fast and in large numbers. </span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">On the contrary, an advanced organism</span><span lang="EN-US"> </span><span lang="EN-US"> or animal</span><span lang="EN-US"> </span><span lang="EN-US"> multiplies relatively very slowly, and in fewer numbers. For example, larger animals such as elephants or humans multiply very slowly, in comparison to a smaller animal such as a rabbit or a primitive organism. </span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">The same is true for a poor, versus a rich society. For example, in poor couples of primitive societies we will find that they usually have between five and eight children. In comparison, the couples in rich societies tend to have one or two children. </span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><b><span lang="EN-US">Cancer environment, diffusion and metastasis</span></b><span lang="EN-US">: When a low energy proliferating cell is found to be lacking the proper nutrition and energy, many times this is so because it is surrounded by an adverse environment. This environment can be an anaerobic (non-oxygenated) one, which is limiting the “energy providing synthesis” of Na and O to K. Shortage of nutrition and energy may also be due to the fact that cells are adjacent or are surrounded by another tumor, or other low energy cells with limited veins and arteries. When a tumor is starving for energy and nutrition, the starvation is transmitted to the neighbors. Obviously, adjacent cells will suffer for proper oxygenation, nutrition and metabolism. Removing energy and nutrition by a tumor from adjacent cells, may cause a similar shortage of energy and nutrition, thus cancer diffusion and cancer metastasis to adjacent cells. </span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span lang="EN-US">We can say, proliferating cells in an energy</span><span lang="EN-US"> </span><span lang="EN-US">crisis, cause a similar “energy crisis” to nearby cells. <u>In other words, the energy crisis of a smaller area of cells, is diffused or extended to a broader area,</u> because of the most basic and fundamental principle of physics</span><span lang="EN-US">, </span><span lang="EN-US">the principle of the conservation of energy and the principle of conservation of matter. </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">This crisis of low energy</span><span lang="EN-US"> </span><span lang="EN-US"> is reflected in the following general chain</span><span lang="EN-US"> </span><span lang="EN-US"> reactions and results</span><span lang="EN-US"> </span><span lang="EN-US">: </span></span> </div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">low transmembrane potential, </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">increased accumulation of sodium ions inside the cell</span><span lang="EN-US"> </span><span lang="EN-US"> : <u>Hypernatremia</u> </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">increased water molecules attached to sodium molecules inside the cell associated to hypernatremia </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">inflammation; </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">increased volume of the cell and osmotic pressure inside the cell, damaging the cell membrane </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">swelling </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">thinning of the cell membrane </span></span></div>
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<span style="font-size: small;"><span lang="EN-US">·</span><span lang="EN-US"> </span><span lang="EN-US">cell division. </span></span></div>
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">The above conditions further obstruct cell metabolism. When transmembrane potential drops below 15 mvolts, it leads to cell</span><span lang="EN-US"> </span><span lang="EN-US"> division and eventually causes cells to over populate. This enhances and diffuses the existing energy</span><span lang="EN-US"> </span><span lang="EN-US"> crisis from the cells to the system. The energy crisis is then extended and generalized for the system as a whole with the characteristic of low energy and ischemia for the system itself. We may say, that cells with low energy get into a “panic” state of feverish multiplication in order to preserve their species, following an inherent program</span><span lang="EN-US"> </span><span lang="EN-US"> encoded in the most fundamental part - their DNA,</span><span lang="EN-US"> </span><span lang="EN-US"> for survival under the emergency of severe conditions. More cells are produced inside the tumor, or more cells are produced adjacent to the tumor which found naturally in a low energy or impoverished environment, diffused from the expanding prime energy crisis – the prime cancer. Newer cancer cells will lack even more energy for the same reasons. So, we see naturally why the tumor grows or diffuses to adjacent areas and tissues, <b>a phenomenon known as “cancer diffusion”</b>, i.e., cancers ability to diffuse to adjacent healthy cells and tissues which is particularly unexplained today by medicine. Obviously, the more those “low energy” cells multiply, more energy is needed in the organism</span><span lang="EN-US"> </span><span lang="EN-US"> as a whole to feed the newborn cells. <b>Therefore, the energy crisis and the cell starvation continually expand, as does cancer. </b></span><span lang="EN-GB"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">The organism</span><span lang="EN-US"> </span><span lang="EN-US"> soon becomes a “poor society in a panic crisis situation” as a whole, lacking even more energy. In such a case, more and more cells will be in a “panic state” for nutrition and energy and so, we see that cancer triumphantly metastasizes and generalizes. The organism or person becomes thin, weak and ischemic, with the common characteristic of loss of weight, low energy, and low nutrition intake. Cancer</span><span lang="EN-US"> </span><span lang="EN-US"> then spreads and generalizes, with no way for the organism or person to overcome this increasing need of energy and nutrition. </span><span lang="EN-GB"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">Apparently, there is <u>no way out of this</u> “energy</span><span lang="EN-US"> </span><span lang="EN-US"> crisis” when many more new cells appear, and the organism</span><span lang="EN-US"> </span><span lang="EN-US"> (or the person) dies. This is more or less the macroscopic “scenario” of the cancer phenomenon. This is of course omitting numerous details of the cell</span><span lang="EN-US"> </span><span lang="EN-US"> physiology, and the details of how the organism gradually fails as a whole. The reason for this is “over population of starving cells” and the resulting expansion of this “energy crisis”. </span><span lang="EN-GB"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">As an indisputable example and confirmation of the above, we may consider the modern technique of cloning living cells through genetic engineering.<b> </b>The technique of cloning living cells consists of forcing a newly fertilized cell (egg) to duplicate into more copies so that one identical embryo develops. This technique simply reported in the mass media consists of isolating a newly fertilized egg and placing it in an environment of very low nutrition. This state of starvation and obviously low energy causes it to divide into copies in exact agreement to the ideas expressed above. </span><span lang="EN-GB"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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<span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"></span></span><span style="font-size: small;"><span lang="EN-US">After a number of divisions into cell</span><span lang="EN-US"> </span><span lang="EN-US">copies, biologists then remove the cell copies and place them in an environment of <b>proper nutrition and energy, where an independent</b> and self organized embryo develops. </span><span lang="EN-GB"></span></span><span style="font-size: small;"><span style="font-family: Arial, Helvetica, sans-serif;"> </span></span><br />
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In some of the latest work, Karl Schoenbach and Stephen Beebe of the Center for Bioelectrics in Norfolk, Virginia, have shown that the pulses can make blood platelets clump together in the first stages of clotting. This is something that might ultimately accelerate wound repair.</div>
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Cell shock</h2>
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Biologists already treat cells with mild electric shocks in the laboratory, a technique called electroporation. These shocks make temporary punctures in cell membranes so that cells can be pumped full of experimental genes or proteins.</div>
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Schoenbach and his colleagues were the first to recognise that you could use high-power, brief shocks to manipulate cells in other ways. Working with electrical engineers in the late 1990s, they discovered that such pulses fry bacteria and sterilize contaminated water.</div>
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One of the most significant discoveries was that nanopulses make mammalian cells commit suicide, rather than blowing them up. This is a relatively gentle way of killing, because scavenger cells come and swallow the debris. By contrast, long electric shocks explode cells and liberate toxic molecules that cause inflammation and pain.</div>
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For this reason, researchers hope to use nanopulses to kill cancer cells while leaving healthy tissue intact. Schoenbach's team has already shown that the pulses can shrink mouse tumours by over 50%, and is working on catheters or non-invasive ways to deliver the shocks to the body.</div>
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Quite how nanopulses trigger cell suicide still leaves scientists scratching their heads. One idea is that the shock flips molecules in the cell membrane from the inside to the outside, which tells surrounding cells of their imminent death. "It says 'get rid of me,'" says Thomas Vernier, who is studying the technique at the University of Southern California, Los Angeles.</div>
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<span style="font-family: Arial, Helvetica, sans-serif;"> However they work, the nanopulses are prompting a flurry of ideas for their use. They might replace liposuction as a way to demolish unwanted flab, or blast away the fatty plaques that cause heart disease. "It is like asking what to do with a newborn baby," says Weaver. "Our speculations probably will not pick up the most important things. </span><br />
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<b><span style="font-family: Arial, Helvetica, sans-serif;">Studies : </span></b> <br />
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<b><a href="http://www.blogger.com/%20http://papimi.com/PAPIMI%20STUDIES/Pappas%20Pysiology%20of%20the%20cell%20manual.pdf">PAPPAS’ PHYSIOLOGY OFTHE CELL AND ITS ATOMIC ENERGY</a></b></div>
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<b><a href="http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2731679/">A new pulsed electric field therapy for melanoma disrupts the tumor’s blood supply and causes complete remission without recurrence - Karl Schoenbach and Stephen Beebe of the Center for Bioelectrics in Norfolk, Virginia</a></b><b> </b></div>
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<b>For more info on how the </b><span style="font-size: small;"><span lang="EN-US"><b>PAP IMI™ Nanopulse Generator can aid to kill off cancerous cells : <a href="http://www.papimiuk.blogspot.com/">www.papimiuk.blogspot.com</a> <a href="http://www.papimi.com/">www.papimi.com</a></b></span></span></div>
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papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-9509519242679600892011-09-03T04:36:00.000-07:002011-09-03T04:38:23.224-07:00Physiological effects of using Papimi Device<div dir="ltr" style="text-align: left;" trbidi="on"><h2 style="font-family: Arial,Helvetica,sans-serif; text-align: justify;">PHYSIOLOGICAL EFFECTS</h2><span style="font-family: Arial,Helvetica,sans-serif;"> </span><br />
<ul style="font-family: Arial,Helvetica,sans-serif;"><li> <div style="text-align: justify;"><span class="long_text" id="result_box0"> <span style="background-color: white;" title="Η αναλγησία, που επιτυγχάνεται με την απελευθέρωση της ενδορφίνης της εγκεφαλίνης, η οποία δρα σαν ανασταλτικό του πόνου."> The analgesia achieved by the release of the endorphin of enkephalin, which acts as an inhibitor of pain. </span></span></div></li>
<li> <div style="text-align: justify;"><span class="long_text" id="result_box0"> <span style="background-color: white;" title="Η ρύθμιση της διαπερατότητας της κυτταρικής μεμβράνης στα ιόντα Να και Κ. Όταν διαταραχθεί η λειτουργία της κυτταρικής μεμβράνης τα ηλεκτρομαγνητικά και ηλεκτρικά πεδία πολώνουν τα κύτταρα και δίνουν σ' αυτά την ενέργεια που χρειάζονται για να αποκατασταθεί η ηλεκτροστατική ισορροπία, θέτοντας την αντλία Κ-Να"> The regulation of membrane permeability to ions Na and K. When the cell membrane is disrupted, the electromagnetic and electric fields polarize the cells and provide them the energy they need to re-establish the electrostatic balance, by restoring the sodium-potassium pump to its normal levels</span><span style="background-color: white;" title="πάλι στην αρχική φυσιολογική λειτουργία της.">. </span> <span style="background-color: white;" title="Με αυτό τον τρόπο τα μαγνητικά πεδία βοηθούν στην υποχώρηση των φλεγμονών και μείωση των οιδημάτων και το κύτταρο λειτουργεί και πάλι φυσιολογικά."> In this way, the magnetic fields help in the reduction of inflammation and edema and as a result the cell functions normally again.</span></span></div></li>
<li> <div style="text-align: justify;">The regulation of glucide<span lang="el">, </span> lipid and protein metabolism, which are the effect of the beneficial influence of the<span lang="el"> </span> <a href="http://en.wikipedia.org/wiki/Sympathetic_nervous_system" target="_blank" title="Sympathetic nervous system">sympathetic</a> and the <a href="http://en.wikipedia.org/wiki/Parasympathetic_nervous_system" target="_blank" title="Parasympathetic nervous system">parasympathetic</a> system.</div></li>
<li> <div style="text-align: justify;">The balance<span lang="el"> </span>of hormone secretion<span lang="el">.</span></div></li>
<li> <div style="text-align: justify;">The strengthening of the immune system by increasing<span lang="el"> </span>the number of leukocytes<span lang="el">των,</span>platelets and<span lang="el"> </span>gamma globulin<span lang="el">.</span></div></li>
<li> <div style="text-align: justify;">The increase of collagen<span lang="el">, </span> due to the reduction of the adenylic acid (AMP).</div></li>
<li> <div style="text-align: justify;">The reduction of osteoclast<span lang="el">s.</span></div></li>
<li> <div style="text-align: justify;">The increase of calcification<span lang="el">,</span> osteoblasts and prostaglandin<span lang="el">.</span></div></li>
<li> <div style="text-align: justify;">The improvement of blood flow and oxygen absorption(oxygenation).</div></li>
<li> <div style="text-align: justify;">Binding free radicals<span lang="el">.</span></div></li>
<li> <div style="text-align: justify;"><span class="short_text" id="result_box1"> <span style="background-color: white;" title="Θετικά αποτελέσματα στην αποκατάσταση τραυματικών καταστάσεων μυών και σε χρόνιες παθήσεις του κινητικού συστήματος."> Positive results in the restoration of traumatic situations of the muscles and chronic locomotor system disorders.</span></span></div></li>
<li> <div style="text-align: justify;">Ant<span lang="el">i-inflammatory</span> effect<span lang="el">.</span></div></li>
<li> <div style="text-align: justify;">The increase of metabolism and biological activity of he cells.</div></li>
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<div style="font-family: Arial,Helvetica,sans-serif; text-align: justify;"><span lang="el"> </span> So far, no adverse effect by the application of Magnetic Fields has been reported and the results are only positive. Finally, the fact that magnetotherapy does not cause temperature raise of the exposed tissues must be underlined.</div></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com0tag:blogger.com,1999:blog-1648381221485527825.post-83305979988215778532011-09-03T04:30:00.000-07:002011-09-03T04:30:17.373-07:00How The Papimi Device Works<div dir="ltr" style="text-align: left;" trbidi="on"> <div style="text-align: justify;"><span class="long_text" id="result_box"> <span style="background-color: white;" title="Τα στοιχεία από τα οποία αποτελείται το ανθρώπινο σώμα, ανάλογα με την επίδραση που ασκούν σε αυτά τα μαγνητικά πεδία διακρίνονται σε:">The elements that make up the human body, according to the influence on these by magnetic fields are divided into: <br />
</span></span></div><ol><li> <div style="text-align: justify;"><span class="long_text" id="result_box"> <span style="background-color: white;" title="Διαμαγνητικά στοιχεία: τα στοιχεία τα οποία επηρεάζονται ελάχιστα από τα μαγνητικά πεδία."> <b>Diamagnetic elements:</b> elements that are affected little by the magnetic fields. </span> <span style="background-color: white;" title="Τέτοια στοιχεία είναι οι υγιείς κυτταρικές μεμβράνες."> Such elements are healthy cell membranes.</span></span></div></li>
<li> <div style="text-align: justify;"><span class="long_text" id="result_box"> <span style="background-color: white;" title="Παραμαγνητικά στοιχεία: τα στοιχεία που επηρεάζονται από το μαγνητικό πεδίο στο οποίο βρίσκονται και μπορούν να μετατραπούν σε μαγνητικά δίπολα με προσανατολισμό ίδιο με τον προσανατολισμό του πεδίου."> <b>Paramagnetic elements:</b> these elements are affected by the magnetic field and can be converted into magnetic dipoles orientated in the same direction of the field.</span></span></div></li>
<li> <div style="text-align: justify;"><span class="long_text" id="result_box"> <span style="background-color: white;" title="Σιδηρομαγνητικά στοιχεία: τα στοιχεία αυτά βρίσκονται κυρίως κοντά στα οστά της βάσης του κεφαλιού, στην υπόφυση, την επίφυση και στο κεντρικό νευρικό σύστημα."> <b>Ferromagnetic elements:</b> these elements are mostly located near the bones of the base of the head, the pituitary, the pineal gland and central nervous system. </span> <span style="background-color: white;" title="Χαρακτηρίζονται από την ύπαρξη σε αυτά περιοχών που τα μαγνητικά τους δίπολα έχουν κοινό προσανατολισμό.">Characterized by the presence in these of regions where the magnetic dipoles have a common orientation. </span> <span style="background-color: white;" title="Τα υλικά αυτά αποκτούν ισχυρές μαγνητικές ιδιότητες όταν βρεθούν μέσα σε πεδίο, τις οποίες διατηρούν όταν το πεδίο πάψει να υπάρχει."> These elements gain strong magnetic properties when found in a field, which are retained when the field no longer exists. <br />
</span></span></div></li>
</ol><div style="text-align: justify;"><span class="long_text" id="result_box"> <span style="background-color: white;" title="Όταν υπάρχει κάποια διαταραχή στον οργανισμό, παρατηρούνται μεγάλες ποσότητες παραμαγνητικών στοιχείων σε αυτόν, ενώ παράλληλα δημιουργείται μία διαφορά δυναμικού ανάμεσα σε μια πάσχουσα και μία υγιή περιοχή."> When there is a disorder in the body, there are large amounts of paramagnetic elements in it, while a potential difference </span> <span style="background-color: white;" title="Όταν υπάρχει κάποια διαταραχή στον οργανισμό, παρατηρούνται μεγάλες ποσότητες παραμαγνητικών στοιχείων σε αυτόν, ενώ παράλληλα δημιουργείται μία διαφορά δυναμικού ανάμεσα σε μια πάσχουσα και μία υγιή περιοχή."> is created </span> <span style="background-color: white;" title="Όταν υπάρχει κάποια διαταραχή στον οργανισμό, παρατηρούνται μεγάλες ποσότητες παραμαγνητικών στοιχείων σε αυτόν, ενώ παράλληλα δημιουργείται μία διαφορά δυναμικού ανάμεσα σε μια πάσχουσα και μία υγιή περιοχή."> between a sick and a healthy region. </span> <span style="background-color: white;" title="Η μεγαλύτερη ποσότητα παραμαγνητικών παρατηρείται επειδή κάποια διαμαγνητικά στοιχεία μετατρέπονται σε παραμαγνητικά.">Most of paramagnetic elements occur because some </span> <span style="background-color: white;" title="Η μεγαλύτερη ποσότητα παραμαγνητικών παρατηρείται επειδή κάποια διαμαγνητικά στοιχεία μετατρέπονται σε παραμαγνητικά."> diamagnetic elements convert into paramagnetic ones. </span> <span style="background-color: white;" title="Με την εφαρμογή μαγνητικών πεδίων επιτυγχάνεται η εξισορρόπηση των παραμαγνητικών στοιχείων και κατά συνέπεια η αποκατάσταση των παθήσεων.">By applying magnetic fields, a balance of paramagnetic elements</span><span style="background-color: white;" title="Με την εφαρμογή μαγνητικών πεδίων επιτυγχάνεται η εξισορρόπηση των παραμαγνητικών στοιχείων και κατά συνέπεια η αποκατάσταση των παθήσεων."> is achieved </span> <span style="background-color: white;" title="Με την εφαρμογή μαγνητικών πεδίων επιτυγχάνεται η εξισορρόπηση των παραμαγνητικών στοιχείων και κατά συνέπεια η αποκατάσταση των παθήσεων.">and therefore the rehabilitation of diseases.</span></span></div><span class="long_text" id="result_box"> <span style="background-color: white;" title="Κάθε κύτταρο (παραμαγνητικό στοιχείο) δέχεται επίδραση κάποιας"> <br />
</span><span style="background-color: white;" title="Το παλμικό μαγνητικό πεδίο διεισδύει στο σώμα ομοιόμορφα, ανεπηρέαστο και επιδρά στην ενδοκυτταρική κίνηση των ιόντων, αυξάνει δηλαδή την διαπερατότητα της κυτταρικής μεμβράνης.">The pulsed magnetic field<span lang="el"> (</span>nanopulses) penetrates the body evenly, unaffected and alters rapidly, it is generated and disappeared in minimum time. According to Faraday's law about induction, a quenching magnetic field leaves behind in its place a circular electric field. In that way, deep inside a tissue electric nanopulses are generated. Nanopulses affect the intracellular traffic of ions, i.e. increase the permeability of cell membranes. </span> <span style="background-color: white;" title="Αποτέλεσμα αυτού είναι η ελάττωση του οιδήματος και του πόνου, η γρήγορη απομάκρυνση των προϊόντων του μεταβολισμού, η αύξηση της παροχής οξυγόνου στην περιοχή, ενώ και τα περιφερειακά κινητικά νεύρα επανακτούν τη λειτουργικότητάς τους.">The result is a reduction of swelling and pain, the rapid removal of products of metabolism, increasing oxygen supply locally, and regional movement nerves regain their </span> <span style="background-color: white;" title="Αποτέλεσμα αυτού είναι η ελάττωση του οιδήματος και του πόνου, η γρήγορη απομάκρυνση των προϊόντων του μεταβολισμού, η αύξηση της παροχής οξυγόνου στην περιοχή, ενώ και τα περιφερειακά κινητικά νεύρα επανακτούν τη λειτουργικότητάς τους."> proper </span> <span style="background-color: white;" title="Αποτέλεσμα αυτού είναι η ελάττωση του οιδήματος και του πόνου, η γρήγορη απομάκρυνση των προϊόντων του μεταβολισμού, η αύξηση της παροχής οξυγόνου στην περιοχή, ενώ και τα περιφερειακά κινητικά νεύρα επανακτούν τη λειτουργικότητάς τους."> function. </span></span></div>papimiukhttp://www.blogger.com/profile/01064913030409476750noreply@blogger.com1