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From the international Amalgam Mailing list : The German Health Ministry has been warning dentists since 1993 not to use palladium-copper alloys any longer. ...especially people who have nickel allergies react to palladium. Adding dental metals like palladium heightens the risk of illness in some people. Palladium/Copper alloys contain up to 10% indium and can cause severe periodontal disease. Contense of Palladium/Copper alloys can be up to 10% Indium, Gallium, Zink, Tin, Cobalt. In Switzerland Palladium dental alloys have been banned. Laboratory tests are showing the following toxic effects: -obstruction of important enzymsystems like creatin-linase, aldolase, alcalite phospatase, carbon-anhydrase, trypsin, chymotropsin -disturbance of collage synthesis like bone and cartilage -obstruction of thymidin in the DNA -accumulation in diff. organs -allergic reactions in people with nickel allergy early symptoms of toxicity: increased salivation pain in teeth and jaw tongue burning cold feeling in mouth metal taste peeling of mucous membrane around teeth fungus like coating in throat and sore throat painful, swollen lymph nodes in the neck late symptoms: dying of teeth granulomas puss pockets with dead tissue swollen tongue systemic early symptoms: extreme nervousness extreme tiredness confusion memory loss dizziness migrane headaches burning of eyes allergies impairment of immune system burning blisters on body systemic late signs: nerve pain in the face paralysis of face muscle cramps of tongue, lips, around eyes sinus infection bronchitis lung ailments without clear reason difficutly breathing at night problems with stomach, intestines, liver, bladder, kidneys weight loss joint and muscle pain muscle cramps and weakness earnoise visual disturbance depression insomnia outbreaks of sweat palpitation difficulty to concentrate ------- Division of Biological Materials der Northwestern University/Chicago. The corrosion resistance of three palladium alloys and one conventional high noble alloy were examined by isolated polarization. Using this method, isolated plots of the cathodic and anodic reaction can be recorded. The corrosion current is given as the anodic and cathodic plots intercept. The current densities of the palladium alloys were approximately ten times higher than of the high noble alloy. All results were dependent on the acidity of the electrolyte. MeSH Terms: Comparative Study Corrosion Dental Alloys/chemistry* English Abstract Palladium* Substances: Palladium Dental Alloys =============== Adverse Health Effects of Palladium Metal cations in dental alloys such as mercury and palladium are continuously released and accumulate in the kidneys, liver, thyroid, brain, CNS, etc.(1,15). Mercury and palladium have high levels of galvanic current densities when near other metals, with the current densities of Pd alloys approx. 10 times higher than for high noble alloys(16). This causes extensive migration of mercury and palladium to saliva, tooth roots, jaw, gums, and other parts of the body(15,16). Like mercury, palladium is cytotoxic and kills or damages cells(12,13,14). Palladium also causes considerable damage and degradation of DNA and exacerbates hydroxyl radical damage (13,14). Palladium also damages cell mitochondria and inhibits enzyme activity and function (9,10,11). Palladium also causes significant numbers of allergic reactions as well as contact dermatitis, stomatitis, lichinoid reactions, and periodontal gum disease(4,5,6,7,8). Because of its toxicity and high mobility, many cases of palladium poisoning have resulted and palladium in dental alloys has been banned in Switzerland, Likewise the German Health Ministry has been warning dentists since 1993 not to use palladium-copper alloys. The warning against using palladium alloys came as a result of poisonings and lab tests in Germany that showed the following toxic effects of palladium: * Obstruction of important enzyme systems like creatin-linase, aldolase, alcalite phospatase, carbon-anhydrease,trypsin, chymotropsin, cellulase; * Disturbance of collage synthesis like bone and cartilage; * Obstruction of thymidin in the DNA; * Accumulation in body organs; * Allergic reaction- esp. for people with nickel allergy. Based on German studies and cases, early symptoms of palladium toxicity include: increased salivation; pain in teeth and jaw; burning tounge; cold feeling in mouth; metal taste, peeling of mucous membrane around teeth; fungus like coating in throat and sore throat; painful, swollen lymph nodes in the neck; extreme nervousness, extreme tiredness, confusion, memory loss, dizziness, migraine headaches, burning of eyes, allergies, impairment of immune system, blisters on body. Late symptoms of palladium poisoning include: dying of the teeth, granulomas, puss pockets with dead tissue, swollen tongue; nerve pain in the face; paralysis of face; muscle cramps of tongue, lips, around eyes; sinus infection, bronchitis and lung ailments without clear reason; difficulty breathing at night; problems with stomach, intestines, liver, bladder, kidneys; weight loss; joint and muscle pain; muscle cramps and weakness; earnoise; visual disturbance; depression, insomnia; outbreaks of sweat, palpitations, difficulty concentrating. References (1) A.Schedle et al, "Response of fibroblasts to various metal cations", J Dent Res, Aug 1995, 74(8):1513-1520. (2) L. Niemi et al, "In vitro cytotoxicity of Ag-Pd-Cu based alloys", J Biomed Mater Res, May 1985, 19(5):549-561. (3) S.Takeda et al, "Corrosion behavior of Ag-Pd alloys and its cytotoxicity", shika Zairyo Kikai, Nov 1990, 9(6):825-830. (4) A.M. Al-roubaie, "Condition of the periodontion of teeth with silver-palladium bridge", Fogorv Sz , Jul 1986, 79(7):207-212. (5) D. Downey, "Contact mucositis due to palladium", Contact Dermatitis, Jul 1989, 21(1):54. (6) J.A.Marcusson, "Contact allergies to palladium chloride", Contact Dermatitis, May 1996, 34(5): 320-323. (7) J.Vilaplana et al, "Adverse oral mucous membrane reactions to dental prostheses", Feb 1994, 30(2): 80-84. (8) A Henston-Pettersen, "Casting Alloy side effects", Adv Dent Res, Sep 1992, 6:38-43. (9) G.M.Kolesova et al, "Effect of Palladium compounds on mitrochondrial enzymatic systems", Vopr Med Khim, sep 1979, 25(5):537-540. (10) J.D. Spikes et al, "Enzyme inhibition by palladium", Biochem Biophys Res Commun, 1969, 8; 35(3);420-422. (11) M.D. Shultz et al, "Palladium- a new inhibitor of cellulase enzyme activity", Biochem Biophys Res Commun, Apr 1995, 209(3):1046-1052. (12) Y Kawata et al, "Cytotoxicity of Pd-Co dental alloys",J Dent Res, Aug 1981, 60(8): 1403- 1409. (13) T.Z.Liu et al, "Palladium exacerbates hydroxyl radical mediated DNA damage", Free Radic Biol Med, 23(1): 155-161, 1997. (14) C.K.Pillai et al, "Interaction of palladium with DNA", Biochem Biophys Acta, Jan 1977, 474(1): 11-16. (15) W.P Bieger et al, "Immunotoxocolgy of metals", Zur Deutshcen Auszahe, 1996. (16) K.bonnig et al, "Quantitative analysis of the corrosion rates of palladium alloys", Dtsch Azhnarztl A 45(8):508-510, Aug 1990. =============== A book written by Daunderer, published by ecomed shows the following symptoms for palladium: Local: Inflammation of mucous membranes (jaw, tongue), periodontal disease, loss of teeth, disturbance of metabolism (bacteria, candida, other fungal infections), metal taste Nervous system: nervousness, headache, lack of concentration, depression, paralysis Immune system: allergy (akne can cover the whole body), cross allergy to nickel, susceptibility to infections, chronic bronchitis, ? of cancer He also states that palladium deposists irreversible in the brain, damages all cells, is a strong nervevous system and immune system poison, a strong allergen with cross reaction to nickel. =========== Bernie, concerning your question about palladium: my bridge consisted of 75% palladium, some platinum, some gold. The palladium has made me sicker than I ever was before. I am not sure how much 3,75% will effect you. Maybe one way to find out is have testing done with vega to see if you react to the stuff, before you spend more money? I was found to have "critical allergy" to palladium by vega testing. The trouble is, you might not react today, but in a few years like it was in my case. The vega test revealed palladium in my nervous system, thyroid, liver, spleen. Testing of the pulled tooth by a German tox-lab revealed a reading of 1,900 ug/kg palladium in the root of the tooth. And was diagnosed with palladium toxicity. It is too bad that dentists in the States are still not aware of the dangers of palladium. I had a chance to talk to several German doctors and have read in the German literature that palladium is as toxic as mercury-amalgam. The symptoms are very much the same I was told, and I can assure you they are at least in my case. I also have talked to people in Germany who had palladium crowns or bridge work done, later had it removed because they got extremly ill. Symptoms vary. One woman developed loss of kidney function, mouth ulcers, gastro intestinal problems. Another one told me that all her mucous membranes dried up, she also has severe problems with overreactions to parfume, car exhausts, blisters and skin problems, and cannot work at the computer any longer. She had some pretty special analysis done showing metals like palladium, gallium, silver, cobalt, lead in her jaw. One woman I am in contact with was diagnosed with MS but in fact had palladium toxicity from a bridge in her mouth. She has gone through extensive DMSA treatments in the meantime and is 90% well. She also had a brain spintogram done with Dr. Koenig in Duesseldorf which showed palladium in her brain. My mother's doctor in Germany told me that palladium "goes into everything". I have to belief that that is true, just from my own case. I just had another tooth pulled, which was o p p o s i t e the palladium bridge under a metal bridge, testing today with vega showed palladium in that tooth root also!!!!!! It also showed silver and copper. The reason I was suspecious was that the root looked all black, just like in the first tooth I had tested. I will send this tooth to the tox lab also to have it analyzed (all this money!!!!). By the way, the vega test of the removed bridge showed thallium in the bridge also. I knew that thallium was somewhere in my dental metals (obviously by mistake). I am still looking for a lab in the States that can analyze for thallium, since the Germans are very expensive, but have not had any luck. My mercury free dentist did not know much about palladium either, but he sure is learning through my case...... About silver and copper. In my case that is also a problem. Copper was found in some of my bridges, so was silver. I react to those too. I am not sure if everybody is as sensitive as I am, but if you have any kind of metal problems like from amalgams, I would stay away from all metals for now. Daunderes advise is really not to put even gold into the mouth after amalgam removal, plus gold is never just gold...... =============== Document 1 Accession No.: 96379291. Second Source: MED/96379291 Author: Finkelstein-Y. Vardi-J. Kesten-M-M. Hod-I. Title: The enigma of parkinsonism in chronic borderline mercury intoxication, resolved by challenge with penicillamine. Source: Neurotoxicology. 1996 Spring. 17(1). P 291-5. Journal Title: NEUROTOXICOLOGY. Abstract: A 47 year old female dentist suffered from hemiparkinsonism which had started eighteen months earlier and was manifested mainly by resting tremor and cogwheel rigidity. A baseline quantitative urinary mercury excretion was 46 micrograms/day. The patient was treated with chelating agent d- penicillamine for a week. Chelation therapy resulted in clinical improvement of parkinsonism and in dynamic changes in daily urinary mercury excretion with a prompt increase to 79 micrograms/day, a subsequent decline followed by increase in the mercury urinary excretion. After a week chelation therapy was stopped. During a follow-up period of five years, the neurological status remained unchanged after the initial penicillamine-induced improvement. This case may be evidence, therefore, of a rare clinical variant of elemental mercury intoxication associated with parkinsonism, in the absence of most classical neuropsychiatric signs of chronic mercurialism. Holdings: Health Sciences Serials SHELVED BY TITLE: Neurotoxicology CALL NUMBER: W1 NE3494HB LIB HAS: v.7(1986)-- =============== Hopefully this is an indication of something good happening! ******************************************* Chelation Therapy is Featured on ABC's Evening News ******************************************* by Michael Evers ABC News with Peter Jennings aired a brief story on chelation therapy Monday, October 13, during the evening news. Here's a transcript of that report: PETER JENNINGS: On our ÑHealth Reportæ tonight, another case of trying to get the insurance companies to pay for a medical treatment that some people think is just the ticket -- in this case, a procedure to unblock clogged arteries that does not require surgery. In fact, the easiest way to understand what happens is to imagine what Drano can do to a clogged pipe. Not everyone in the medical community is sold on this experimental therapy. But a growing number of people are. And here is ABCºs John McKenzie. JOHN MCKENZIE, ABC NEWS: For Alan Hay, the memories are all so vivid. He was 51 years old and about as rugged as they come. He owned a guest ranch in Montana, worked as a trail guide and ran a logging business. Then a heart attack two years ago brought a sudden and profound change. ALAN HAY: Just the normal everyday things that you take for granted are suddenly gone. Just walking, getting out of bed, climbing up stairs was very difficult. JOHN MCKENZIE: So Hay signed up for a controversial treatment to open his clogged arteries. It is called chelation, a therapy now so popular that half a million Americans use it each year. It's an intravenous drip that passes through the arteries, removing calcium deposits that contribute to clogging. DR RICHARD ASH, INTERNIST: With chelation therapy, we're able to increase blood flow and then reduce the need for medication and surgery. So therefore, there are fewer side effects and complications. JOHN MCKENZIE: A series of 20 chelation treatments -- that's about the average -- can cost a total of $2,000. The problem is insurance companies won't pay for it. Although chelation has been approved for ridding the body of heavy metals, such as lead and mercury, it has not been sanctioned for use in heart disease and the opening of arteries, even though many patients report profound benefits. DR MORIE GERTZ, MAYO MEDICAL CENTER: The questions can only be answered scientifically. I think physicians simply recognize that there are not substantive meaningful studies published that demonstrate it is effective. DR PATRICK FRATTELONE, CARDIOLOGIST: Keep on going for 13 minutes. JOHN MCKENZIE: But Alan Hay and his doctor are convinced. After 20 chelation treatments, he completed a rigorous stress test. DR PATRICK FRATTELONE: After a heart attack, you expect the function of the heart to be abnormal, and in this case, his heart looks like it didn't even have a heart attack. JOHN MCKENZIE: Is that unusual? DR PATRICK FRATTELONE: Very unusual. ALAN HAY: I feel better now than I did before I had the heart attack, to be honest with you. I'm in great shape. JOHN MCKENZIE: These cases are now common enough that some doctors say it's time to finally put this treatment to the test with a large, tightly controlled clinical trial to see whether a relatively simple therapy is actually responsible for some remarkable recoveries. John McKenzie, ABC News, New York. PETER JENNINGS: If you'd like some more information about this topic, you can contact us at health@abcnews.com. For more information, ABC News Health Report -- Unblocking Clogged Arteries: Getting Insurance Companies to Pay for Chelation http://www.abcnews.com/onair/wnt/html_files/transcripts/wnt1013.html American College for Advancement in Medicine http://www.acam.org/ (714) 583-7666 ============== Diane, For the bridge you might consider Purealloy by Purealloy Lab in Colorada Springs, Colorad. It's mostly gold with a little titanium. Have you had biocompatibility testing. It's probably worth it if you are having problems and going to spend a lot of money. For the retreatment of the root canal and sealing it consider Bio-Calex (calcium oxide). Sam could tell you more about that. Do a web search for Bio-Probe. My chelation doctor doesn't think there is much harm in doing chelation before all fillings are out. He follows up DMPS treatment with a Vit C/mineral IV. If you are having joint/arthritic problems try glucosamine sulfate. It's documented in clinical trials to work and I know several for whom it has done wonders. You can get it in any Health Food Store. Bernie ============ Monosodium glutamate (MSG) is used in relatively enormous quantities (compared to the West) in Chinese cooking as well as in the food of various other Asiatic countries. It has long been known, or rather suspected, that a small minority of Westerners are hypersensitive to this food additive: Per, I believe that persons who are recovering from amalgam toxicity should *definately* avoid aspartame because of the potential formaldehyde problems (among other things). I also believe that free form excitotoxic amino acids (which often include a variety of poorly-tested impurities) such as MSG and aspartic acid from aspartame should be avoided as well. I believe that MSG use is relatively rare in China (but is used in Westernized Chinese restaurants quite a bit). It is used quite a bit in Thailand and some other Asian countries. However, it is used in fairly large quantities in the U.S. as well. Once one realizes that virtually every statement and "fact" which is produced by the aspartame/MSG industry is provably untrue, then it becomes necessary to look closer at these usage surveys conducted by the industry. It turns out that very old surveys show low usage of MSG in the U.S. Newer surveys do not take into account the fact that the industry now hides MSG in food ingredients which are then added to foods unlabelled. MSG usages in Europe, however, appears to be relatively low at this point in time. quoted text: "There have been numerous challenges of MSG-induced adverse reactions in individuals, all of which have failed to reproduce the symptoms associated with Chinese restaurant syndrome," said Steve Taylor, Ph.D., professor and head of the Food Science Department at the University of Nebraska. Studies measuring objective responses such as blood pressure, heart rate, skin temperature and muscle tone have been unable to detect differences between persons fed MSG and placebo. This is an example of outright dishonesty in the scientific community regarding potentially toxic substances. It is toleration of statements like this (whether they comes from the aspartame, MSG, fluoride, amalgam, tobacco, breast implant, etc. industries) which is why myself and I believe a very large and growing number of others rely on common sense, grandma's advice, and quite a few other things long before putting faith in the scientific community. Of course, myself and many others do not start out with such a strong view. Many people will prefer to wait 10, 20, 100 years until special interest groups have finally been overcome by honest scientists. That is fine, but I don't recommend it. There are quite a few studies (including several double-blind studies) showing that MSG causes adverse reactions (including some potentially serious reactions). One researcher estimated 30% will react to MSG at 5 grams (an amount found in some restaurant meals). What Dr. Taylor is neglecting to mention is that it is only industry-funded studies which never show any increase in reactions in the test group above the placebo group. Perhaps this is because all industry experiments since 1978 had aspartame (which breaks down into an excitotoxic amino acid like MSG, methanol, etc.) hidden in the beverage mixture given to both groups. This fact was hidden from the scientific community and the public and was only discovered many years later because of an inadvertant disclosure by an International Glutamate Technical Committee official. There are, of course, many other major flaws in these industry experiements which would account for the lack of increase in reactions found. Please see the Aspartic Acid chapter in the draft review on my aspartame web page. http://www.tiac.net/users/mgold/aspartame/aspartame.html quoted text: Currently all foods with added MSG must list the ingredient on the label as monosodium glutamate. FDA recently announced it may broaden the requirement to require listing of glutamate when it is a significant functional component of other ingredients such as hydrolyzed protein. In the U.S., the labelling laws allow the food industry to put MSG into a *food ingredient* and then add that ingredient to the food without having to label the MSG. They can also add a wide variety of forms of glutamic acid below 99% pure glutamic acid and avoid calling it MSG. It's a game that the food industry calls "Clean Labels." In announcing the change, FDA underscored that the decision is due to public interest in the issue and not from any health concern about MSG's safety. The tentative final regulation is expected to be published in mid-1992. The FDA sat on this proposal for years because the food industry was against it. It was only a recent lawsuit by the Truth in Labelling Committee which forced the FDA to start taking action in order to impress the judge in hopes of getting the suit dismissed. Please see: http://www.annapolis.net/members/holland At http://ificinfo.health.org/brochure/msg.htm is a document dated September 1991 with the title "What You Should Know About MSG". There MSG is described as extremely safe. IFIC is a junk food industry-funded PR organization. I can virtually guarantee that they would find mercury amalgams perfectly safe had reviewed that literature. The accuracy of the information given out by IFIC is on the same level as that given out on amalgams by the NCAHF -- a significant amount of convincing-sounding, provably inaccurate or irrelevant information. Many people with ALS seem to shun MSG. I don't know the evidence on the hazards of MSG, but one of the basic facts of the case must certainly be that MSG is used in large quantities by whole populations in Asia without apparent ill effects. On the whole, I should think, the dietary habits of the peoples involved are much less foolish than those of average Westerners. And there is no money in MSG as such. I can buy it very cheaply in 500 g bags in a nearby town. One might say that "mercury amalgam is used by countless millions without apparent ill effects." While acute reactions to MSG appear to be lower in Asia, the much more serious concerns of damage from the excitotoxic effects may very well be effecting the countries where it is used in large amounts. The industry is fond of making statements that such effects are not seen in these countries. However, looking at the scientific literature in Thailand and the U.S., one can see a trend of neuroendocrine and reproductive disorders similar to what is seen in the excitotoxic amino acid experiments in animals. Please see the Aspartic Acid chapter of the draft aspartame review mentioned earlier. The money from MSG comes in the huge volume sold in some parts of Asia and in the U.S. FORMALDEHYDE IN ASPARTAME: ABSTRACT: The level of aspartame in a can of Diet Coke was found to be 0.06% by a food testing laboratory. The remaining cans from one case of .... percent aspartame, 0.001 percent DKP and 53.5 parts per billion of formaldehyde. The room temperature sample contained 0.051 percent aspartame, 0.002 percent DKP and 231 parts per billion of formaldehyde. .... Is a concentration of 231 parts per billion (ppb) of formaldehyde hazardous? I don't know, but it depends of course on how much Coke you drink. The U.S. Department of Labor, Occupational Safety & Health Administration have a document on formaldehyde at http://www.osha-slc.gov/OshStd_data/1910.1048.html. This is centered on concentrations in indoor air (8-hour exposure), which is of course not the same as food safety, but it appears that concentrations below 500-750 ppb are not considered hazardous (Permissible Exposure Level, PEL). Again, I am asking because I am ignorant, and because I am interested in these important problems. The OSHA figures are based on inhalation exposure. I posted earlier about formaldehyde and composites asking how much, if any, is inhaled: The Wantke (1996) study showed chronic adverse effects in children at levels starting around 0.05 ppm [50 ppb] and a couple of listed in National Research Council (1981, page 186) show adverse effects starting near that level. (Apparently children are sensitive at lower levels than adults.) I believe that formaldehyde is much more toxic when inhaled as opposed to ingested. This may be because less is absorbed or it is quickly converted by the liver to CO2 as discussed in Owen (1990). The question then becomes how much formaldehyde from the composites are *inhaled* as opposed to ingested. I also wonder if it varies from composite to composite. Finally, I wonder if any of the compounds inhaled together could lead to a synergistic adverse effect. Dagfin pointed out (I believe) that only an extremely small amount of formaldehyde is released from composite fillings and primarily in the first days after the cavity is filled. I believe that the overwhelming majority of formaldehyde from aspartame comes from the methanol part which is absorbed and then converted to formaldehyde. That, in my opinion, is a bigger concern for those who are trying to avoid slow poisoning. Best Wishes, ============ Thallium is chemically related to plumbum and toxicologically to plumbum and arscnicum. It affects mainly the nervous system, some of its effects probably due to disturbances of the peripheral and sympathetic nerve, others to disturbances of the peripheral motor and sensory nerves. In addition it produces hypochlorhydria, gastroenteritis. nephritis, folliculitis of the hairs and various skin symptoms. Mind : Irritability, oversensifivitv (cries or shouts at the least provocation), later apathy, dullness, delirious states, sometimes euphoria, dementia. General: Loss of weight, fatigue, as if after a severe sickness, Epileptic attacks. Head: Headaches, pains in occiput. Every morning strong occipital pain lasting one hour, Eyes: Dilation of pupils. Conjunctivitis and Blepharitis. Ulcer of cornea, Ptosis, Retrobulbar nephritis, central scotoma for red and green. Digestive tract: Stomatitis; Glossitis: dryness, burning, salivation. Loss of appetite, nausea, vomiting. Cramps in stomach and abdomen, lancinating pains. Diarrhoea and constipation. Urinary and genital tract: Tenesm, involuntary urination, polyuria, nephritis, eystitis. Impotence. Amenorrhoea. Respiratory organs: Shortness of breath, oppression of chest, drawing pains, Bronchitis. Broncho-pneumonia. Heart and circulation: Tachycardia. Anginal pains. Elevation of blood pressure with slow pulse. Coldness of hands and feet. Nervous system: Lancinating, drawing, boring, burning, violent, intolerable pains, not relieved by analgesics, incl. Morphine; pains particularly, in legs with paresthesias, tingling, numbness, sensation of coldness or burning. Sensation "as if wet felt were placed around legs," "as if legs were lying in glass splinters" "as if legs were enlarged": terrible pains in fingertips: clawposition of fingers and toes: pains in legs worse from standing and stepping. Tosses in bed, moaning with pains. Arthralgia. Decreased sensitivity for touch, at the same time hypersensitivity of skin; cannot bear to be touched: does not dare to breathe or eat because of pain. Worse from pressure of bed and clothing. Worse from motion. Periodicity of pains. Loss of reflexes, paresis and paralysis of muscles. Choreatic movements. Sleep: Insomnia, not affected by hypnotics. Somnolence. Shin: Outbreaks of perspiration. Pustules. Herpes. Hyperkeratosis of palms and soles. White lines across the nails, Loss of hair, particularly of scalp. Characteristics of Thallium: Intense, lancinating pains, not influenced by analgetics, (probably of central origin) with hypersensitivity of the skin and paraesthesia, coldness of painful parts, or intense burnign. Alopecia. Neuritis and paralysis. Clinical suggestions: Neuralgia, neuritis, polyneuritis, tabes dorsalis. Retrobulbar nemitis. Alopecia. - Journal of the American Institute of Homeopathy, Sept. 1951 Top |