Mercury  From  Amalgam Fillings:   A Major Factor in Periodontal Disease and Oral Health Problems


I.      Introduction & Mercury Exposure Levels from Amalgam

     Mercury is one of the most toxic substances in existence and is known to bioaccumulate in the body of people and animals that have chronic exposure.  Mercury exposure is cumulative and comes primarily from 3 main sources: occupational exposure, food (mainly fish), and silver/mercury dental fillings. Whereas mercury exposure from fish is primarily methyl mercury, mercury from occupational exposure and dental fillings is primarily from elemental mercury vapor. But bacteria in the mouth and intestines methylate other forms of mercury to methyl, and some demethylation also occurs.  

The most common type of occupational exposure comes from dental office exposure and is documented to result in significant adverse health effects (602).  Mercury in amalgam fillings, because of its high volatility and galvanic action due to presence of dissimilar metals in the mouth, has been found to be continuously vaporized and released into the body (192,600, etc.), and has been found to be the  largest source of   mercury  in the majority of people who have amalgam fillings (WHO:183,199,209,601, 18). The level of daily exposure commonly exceeds the U.S. EPA health guideline for daily mercury exposure (2,217,601).   EMF and wi-fi  exposures have been found to increase the mercury vapor release by amalgams and thus increase toxicity effects. Metal crowns, amalgams, and metal implants also cause an antenna effect regarding microwaves, etc.- causing additional adverse effects along with the metals reactivity many have. 

Concentrations of mercury in oral mucosa for a population of patients with 6 or more amalgam fillings taken during oral surgery were 20 times the level of controls (174).  Studies have shown mercury travels from amalgam into dentin, root tips, and the gums, with levels in roots tips as high as 41 ppm (192). Studies have shown that mercury in the gums such as from root caps for root canaled teeth or amalgam tattoos result in chronic inflammation, including proliferation of inflammatory cytokines in addition to migration to other parts of the body (200,47,35, 86a,314a).  Mercury and silver from fillings can be seen in the tissues as amalgam tattoos, which have been found to accumulate in the oral mucosa as granules along collagen bundles, blood vessels, nerve sheaths, elastic fibers, membranes, striated muscle fibers, and acini of minor salivary glands.  Dark granules are also present intracellularly within macrophages, multinucleated giant cells, endothelial cells, and fibroblasts, and metals also accumulate in tooth roots and the jaw bone (47,35).  There is in most cases chronic inflammatory response or macrophagic reaction to the metals (47), usually in the form of a foreign body granuloma with multinucleated giant cells of the foreign body and  Langhans  types (192). In a group of patients with amalgam tattoos that were tested, 74% of the patients revealed high lymphocyte reactivity (positive MELISA test) to one or more metal components of dental restorations(47k). The majority of MELISA positive patients suffered from serious health problems (various allergies, autoimmune diseases, Parkinson's syndrome etc.). Nickel and inorganic mercury were the most common sensitizers in vitro. The cytokine assay revealed that mercury chloride activated predominantly TH2 lymphocytes, while nickel chloride activated mainly TH1 lymphocytes. 

Most dentists are not aware of the main source of amalgam tattoos, oral galvanism where electric currents caused by mixed metals in the mouth take the metals into the gums and oral mucosa, accumulating at the base of teeth with large fillings or metal crowns over amalgam base (192). Such mercury including that in the commonly formed amalgam tattoos moves to other parts of the body over time in significant amounts and more rapidly than the other metals. Macrophages remove mercury by phagocytosis and the mercury moves to other parts of the body through the blood and along nerves (47). Another study (47l) demonstrated a dense mononuclear inflammatory infiltrate associated with large and powdered debris and positivity for HLA-DR and MT in inflammatory cells. While blood vessel walls and connective fibers impregnated with powdered particles were negative for HLA-DR, they were positive for MT. In addition, wherever epithelial basement membrane impregnation by powdered amalgam particles was observed, a strong positivity for MT was detected. These findings demonstrate that residual elements of AT still have noxious local effects over tissues.  Such metals are documented to cause local and systemic lesions and health effects, which usually recover after removal of the amalgam tattoo by surgery (47fghim). The high levels of accumulated mercury also are dispersed to other parts of the body .

       Mercury vapor given off by amalgam fillings accumulates in the teeth, tooth roots, gums, jawbone, and oral tissue.  The number of amalgam surfaces has a statistically significant correlation to the level of mercury in oral mucosa and saliva (18,77,79,182,199,211,222,292). Those with dental amalgams commonly have metal immune reactivity with corresponding immune, autoimmune, and allergic conditions (60,313,369, etc.) The most common metals that patients have immune reactivity to are nickel, gold, mercury, palladium, and titanium (60). The immune reactivity and health problem usually significantly improves after metal replacement. The Melisa immune reactivity test was found more effective than the patch test in such patients. 


The amount of mercury in saliva averaged between 1.5 to 1.9 micrograms per Liter for each amalgam filling(199ab).  

     The amount of mercury released by a gold alloy bridge over amalgam over a  10 year  period was measured to be approx. 101 milligrams(mg) (60% of total) or 30 micrograms(ug) per day (18), and other studies have found similar results (182).  The average mercury levels in gum tissue near amalgam fillings are often over 100 ppm (192), and levels in oral mucosa removed during oral surgery averaged over 2  ppm( over 20 times controls ) and levels in root tips of 41 ppm(174,192,47).  

      Having dissimilar metals in the teeth ( e.g. ‑gold and mercury) causes  galvanic action , electrical currents, and much higher mercury vapor levels and mercury levels in tissues. (182,191,192,18,19,27, 30,47,48,8,174).   The level of mercury in the gums or jaw bone is often 1000 ppm near a gold cap on an amalgam filling (30,25,35,48,58), and similar levels as high as 5600 ppm have been found in the jaw bone under large amalgam fillings or gold crowns over amalgam by German oral surgeons (436).  These levels are among the highest levels ever measured in tissues of living organisms, exceeding the highest levels found in chronically exposed  chloralkali  workers, those who died from  mercury  in  Minamata, or animals that died from mercury poisoning.  The FDA action level for warnings of dangerous levels in fish or  food  is  1 ppm and the EPA health criterion level is 0.3 ppm. In patients with galvanic cell in their oral cavity we found decreased levels of anti-inflammatory markers, such as secretory IgA, IgA 1, IgA 2, and lysozyme, and increased levels of the proinflammatory marker albumin (192i).   

Amalgam also releases significant amounts of silver, tin, and copper which also have toxic effects, with organic tin compounds formed in the body being even more neurotoxic than inorganic mercury.

        German studies of mercury loss from vapor in unstimulated saliva found the saliva of those with amalgams had at least 5 times as much mercury as for controls (179,199].  Much mercury in saliva and the brain is also organic, since mouth bacteria convert inorganic mercury to methyl mercury (81,88,600). Oral bacteria  streptococommus   mitior,S .mutans , and  S.sanguis  were all found to methylate mercury(81,600),as well as Candida albicans.  Methyl mercury, like mercury vapor, crosses the blood-brain barrier, and both forms are converted to very neurotoxic inorganic compounds which have a long half-life in the brain. The process also  results  in  formation of hydrogen sulfide and metal protein compounds that are involved in mouth odor(334).

        A large U.S. Centers for Disease Control epidemiological study, NHANES  III,  found  that those with more amalgam fillings(more mercury exposure) have significantly higher levels of chronic health conditions(543a).     A 2009 study found that inorganic mercury levels in people have been increasing rapidly in recent years(543b). It used data from the U.S. Centers for Disease Control and Prevention�s National Health Nutrition Examination Survey (NHANES) finding that while inorganic mercury was detected in the blood of 2 percent of women aged 18 to 49 in the 1999-2000 NHANES survey, that level rose to 30 percent of women by 2005-2006. Surveys in all states using hair tests have found dangerous levels of mercury in an average of 22 % of the population, with over 30% in some states like Florida and New York(543c).

II.    Oral Health Effects of Mercury from Amalgam

    A large study of 20,000 subjects at a German university found a significant relation between the number of amalgam fillings with periodontal problems (199).    Some of the oral effects documented in the literature to be caused by amalgam  include gingivitis, oral gum tissue inflammation, bleeding gums, bone loss, mouth sores, oral lesions, pain and discomfort, burning mouth(89), metallic taste, chronic sore throat, chronic inflammatory response, lichen planus autoimmune response, oral keratosis, oral cancer (251,252) , bad breath, mouth dryness, tender teeth,  trigeminal neuralgia, sinusitis, TMJ,  orafacial  granulomatosis, oral lichen planus (86-90,95) , leukoplakia, amalgam tattoos,  etc.  (27,29,48a,86-90,95,192a, 303,341,525a,582,5). Amalgams are also a factor in periodontal disease (303, etc.).      Removal of amalgam fillings led to cure or significant improvement for most of such oral health problems  (8,27,56,57,75,82,86,87,90,94,95,101,115,133,145, 167,168, 192abcf,212,222,233,303,313,317,320,321, 341,525a,582, etc.) and oral keratosis (pre cancer) (87,251,252). For example, in one clinic (95) that replaced amalgams for a large number of such patients, there was cure or significant improvement in over 90% of cases for metallic taste, tender teeth, mouth sores, and bad breath  and  in  over 80% of cases for bleeding gums and throat irritation.  A Jerome meter was used to measure mercury vapor level in the mouth, and many had over 50 micrograms mercury per cubic meter of air, far above the Government health guideline for  mercury( 217).

Mercury accumulates in the trigeminal ganglia (325,329ab,303) and can cause trigeminal neuralgia from which most recover after amalgam replacement(525a,192a,35d,222,437b,303).  Temporomandibular joint disorder (TMJ) is a common type of joint pain which can be caused by accumulation of mercury in the joint due to the high amount of mercury in the mouth area of those with amalgam fillings and due to inflammation, similar to arthritic effects on other joints caused by mercury (303).  Accumulation of mercury in the cranial nerves is a common cause of tinnitus, TMJ, cataracts, loss of smell, etc. (303). 

Cavitations  from improperly healed tooth extractions also commonly cause trigeminal neuralgia and most such recover after cavitation surgery(437b,35a).   The periodontal ligament of extracted teeth is often not fully removed and results in incomplete jawbone regrowth resulting in a pocket (cavitation) where mouth bacteria in anaerobic conditions along with similar conditions in the dead tooth produce extreme toxins similar to botulism which like mercury are extremely toxic and disruptive to necessary body enzymatic processes at the cellular level, comparable to the similar enzymatic disruptions caused by mercury and previously discussed(35,437ab). 

Extremely toxic anaerobic bacteria from root canals or  cavitations  formed at incompletely healed tooth extraction  sites  have  also been found to be common factors in Fibromyalgia and other chronic neurological conditions such as Parkinson�s and ALS, with condensing osteitis which must be removed with a surgical burr along with 1 mm of bone around it(35,200,437ab).   Cavitationshave been found in 80% of sites from wisdom tooth extractions tested and 50% of molar extraction sites  tested( 35,200,437ab).  The incidence is likely somewhat less in the general population. 

.        The interruption of the ATP energy chemistry results in high levels of porphyrins in the  urine( 260).   Mercury, lead, and other toxics have different patterns of high levels for the 5 types of porphyrins, with pattern indicating likely source and the level extent of damage.   The average for those with amalgams is over 3 time that of those without, and is over 20 times normal for some severely poisoned  people( 232,260). The FDA has approved a  test measuring porphyrins  as a test for mercury poisoning.     However  some other dental problems such as nickel crowns,  cavitations , and root canals also can cause high porphyrins.   Cavitations  are diseased areas in bone under teeth or extracted teeth usually caused by lack of adequate blood supply to the area. Tests by special equipment ( Cavitat ) found  cavitations  in over 80% of areas under root canals or extracted wisdom teeth that have been tested, and toxins such as anaerobic bacteria and other toxics which significantly inhibit body enzymatic processes in virtually all  cavitations  (200,437ab).  These toxins have been found to have serious systemic health effects in many cases, and significant health problems to be related such as arthritis, MCS, and CFS.  These have been found to be factors along with amalgam in serious chronic conditions such as MS, ALS, Alzheimer�s , MCS, CFS, etc. (35,200,204,222,292,437).  The problem occurs in extractions that  are  not  cleaned out properly after extraction.  Supplements such as glucosamine sulfate and avoidance of orange juice and caffeine have been found to be beneficial in treating arthritic conditions as well (35).


          Nickel and beryllium are 2 other metals commonly used in dentistry that are very carcinogenic, toxic, and cause DNA malformations (35,456).  Nickel ceramic crowns, root canals and  cavitations  have also been found to be a factor in some breast cancer and other cancers and some have recovered after TDR, which includes amalgam replacement, replacement of metal crowns over amalgam, nickel crowns, extraction of root canaled teeth, and treatment of  cavitations  where necessary (35,200,228a,486,530).  Similarly nickel crowns and gold crowns over amalgam have been found to be a factor in lupus (456,35,229) and  Belle�s  Palsy from which some have recovered after TDR and  Felderkrais  exercises (35).  An analysis of the large U.S. NHANESIII population found that the age-adjusted geometric mean urine Cadmium concentration was significantly higher among participants with periodontal disease (241.)  Smoking is known to be a common source of elevated cadmium level. 

     Toxic/allergic reactions to toxic metals such as mercury/amalgam often result in autoimmune conditions such as lichen planus lesions in oral mucosa or gums, eczema, pustulosis, dermatitis and play a  roll  in pathogenesis of periodontal disease (85-88,90,313, 314,303, etc.). A high percentage of patients with oral mucosal problems along with other autoimmune problems such as chronic fatigue (CFS) have significant immune reactions to mercury, palladium, gold, and nickel (313,118,369).  94% of such patients had significant immune reactions to inorganic mercury (MELISA test) and 72% had immune reactions to low concentrations of HgCl2(<0.5 ug/ml). 61% also had immune reaction to  phenylHg , which has been commonly used in root canals and cosmetics (313).  Removal of amalgam fillings usually results in cure of such lesions. [75,82,86,87,90,94,101,118,133, 145,167,168,313].  Patients with other systemic neurological or immune symptoms such as arthritis, myalgia, eczema, CFS, MS, diabetes, etc. also often recover after amalgam replacement (313,118,369,86,600, etc.)  10% of controls had significant immune reactions to  HgCl  and 8.3% to palladium.

        In a recent study of patients with OLP, 60 % showed sensitization to 1 or more allergens using a patch test (85). The greatest frequency of positive reactions was to dental metals.  The order of tested metals according to frequency of positive reactions was mercury, amalgam, nickel, palladium, cobalt, gold, chrome, and indium. However, patch tests have been found to not be a reliable indicator of mercury immune reactivity or allergy (303, etc.).  In large number of clinical trials by doctors treating OLP, between 39 and 53% of patients tested by patch tests were indicated to be reactive to mercury.  However, when patients had amalgams replaced, the majority recovered or significantly improved in a relatively short time period-  irregardless  of patch test results. Thus, the authors recommend replacement of amalgam in all cases of OLP and similar conditions.  The MELISA blood lymphocyte immune reactivity test appears to be a more accurate indicator of immune reactivity than the patch test.  When patch tests are to be used it should be noted that the clinical trials found that mercury immune reactivity is often a delayed reaction, with positive patch test observed only later on the 10th or 17 th  day of the test.  Patients with OLP also commonly have been found to be immune reactive to gold or nickel so that replacement of gold or nickel crowns may be beneficial in such patients when amalgam replacement is not sufficient to resolve the problem (85). 

        Oral lichen planus and oral lesions, caused most commonly by reactivity to mercury, are inflammatory pre-cancerous conditions that have been well documented in the literature to often develop into oral squamous cell carcinoma (OSCC )( 85).   Infection and chronic inflammation have been found to contribute to carcinogenesis through inflammation-related mechanisms (85).  Inflammatory bowel diseases are associated with colon carcinogenesis and inflammatory oral conditions such as oral lichen planus (OLP) and leukoplakia are associated with OSCC. 


    Mercury (as well as toxins from root canals and  cavitations ) interact with brain tubulin and disassembles microtubules that maintain neurite structure (207b,258,35,200,303,437).  Thus, chronic exposure to low level mercury vapor can inhibit polymerization of brain tubulin and creatinine kinase which are essential to formation of microtubules.  Reviews of mercury studies on animals give results similar to that found the Alzheimer brain.  The effects of mercury with other toxic metals have also been found to be  synergistic , having much more effect than with individual exposure (35).

Teeth are living tissue and have massive communication with the rest of the body via blood, lymph, and nerves. Mercury vapor (and bacteria in teeth) have paths to the rest of the body. (34,325, etc.)  Mercury has direct routes from the teeth and gums to the brain and CNS, where it accumulates to high levels in those with a large number of amalgam fillings (34,327,329).  Cytotoxic effects of dental amalgam, measured by  the frequency of micronuclei (MN) in oral mucosal cells, as it is a promising tool for studying the genotoxic effect of clastogenic agents on them, were significantly higher than for composite restorations, and higher for multiple restorations than for single restorations (59). 


        Due to galvanism of mixed metals, amalgam fillings produce electrical currents which increase mercury vapor release and may have other harmful effects (14,19,27-30,35,47, 100,192, 600).   These currents are measured in micro amps, with some measured at over 4 micro amps. The central nervous system operates on signals in the range of nana-amps, which is 1000 times less than a micro amp (28). The metals also have electrical potentials which can be measured in millivolts(mV).  One clinical study determined that electrical potential differences of over 50 mV were pathological(48b), causing galvanism, leukoplakia, oral lichen planus, or toxic or allergic reactions to restorations (48a, etc.). In most subjects with amalgam fillings, potential differences of more than 50 mV are present between restorations(48a), with potentials ranging from -417 mV to +150 mV. Negative potentials may be more pathological than positive ones.   The average potential for metal crowns and bridges was 154 mV and for brace brackets was 74 mV(48a). 

       Negatively charged fillings or crowns push electrons into the oral cavity since saliva is a good electrolyte and cause higher mercury vapor losses (35,192).   Patients with autoimmune conditions like MS, or epilepsy, depression, etc. are often found to have a lot of high negative current fillings (35).  The Huggins total dental revision (TDR) protocol calls for teeth with the highest negative charge to be replaced first (35).  Other protocols for amalgam removal are available from international dental associations like IAOMT (153) and mercury poisoned patient�s organizations like  DAMS (447).    For these reasons it is important that no new gold dental work be placed in the mouth until at least 6 months after replacement.    Some studies have also found persons with chronic exposure to electromagnetic fields (EMF) to have higher levels of mercury exposure and excretion (28).  The post MRI saliva mercury levels for a sample of patients was on average 31% higher after MRI than before(28e).

    In a large German study of MS patients after amalgam revision, extraction resulted in 80% recovery rate versus only 16% for filling replacement alone (302,308). Other cases have found that recovery from serious autoimmune diseases, dementia, or cancer may require more aggressive mercury removal techniques than simple filling replacement due to body burden. This appears to be due to  migration of mercury into roots and gums that is not eliminated by simple amalgam replacement. , providing a lasting residue for chronic mercury exposure.  That such mercury (and similarly bacteria) in the teeth and gums have direct routes to the brain and CNS has been documented by several medical studies (34,325, etc.). 


       Periodontal offices also often are a source of exposure to mercury for staff and patients. Both dental hygienists and patients get high doses of mercury vapor when dental hygienists polish or use ultrasonic scalars on amalgam surfaces (240).   Pregnant women or pregnant hygienist especially should avoid these practices during pregnancy or while nursing since maternal mercury exposure has been shown to affect the fetus and to be related to birth defects, SIDS, etc. (38,61,272), and breast milk contains up to 6 times higher mercury than in the mother's blood (20,186). There is considerable exposure as well when polishing amalgam fillings and hygienists are generally advised not to polish amalgam fillings. 


    The component mix in amalgams has also been found to be an important factor in mercury vapor emissions.  The level of mercury and copper released from high copper amalgam is as much as 50 times that of low copper amalgams (191).  Studies have consistently found modern high copper  non gamma -two amalgams have greater release of mercury vapor than conventional silver amalgams (298).   While the  non gamma -two amalgams were developed to be less corrosive and less prone to marginal fractures than conventional silver amalgams, they have been found to be unstable in a different mechanism when subjected to wear/polishing/ chewing/ brushing/bleaching, etc. they form droplets of mercury on the surface of the amalgams (297,136,182,192).  This has been found to be a factor in the much higher release of mercury vapor by the modern  non gamma -two amalgams.   Recent studies have concluded that because of the high mercury release levels of modern amalgams, mercury levels higher than Government health guidelines are being transferred to the lungs, blood, brain, CNS, kidneys, liver, etc. of large numbers of people with amalgam fillings and widespread neurological, immune system, and endocrine system effects are  occurring( 34,35,199,212,222,313,118,600). 


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(308) Max  DaundererHandbuch  der  AmalgamvergiftungEcomed  Verlag, Landsberg,1998, ISBN 3‑609‑71750‑5 (in German)

(313) �Mercury-specific Lymphocytes: an indication of    mercury allergy in man�, J. Of Clinical Immunology, 1996, Vol 16(1);31-40  V.D. M.Stejskal  et al;  ; & Perioral dermatitis after dental filling in a 12-year-old girl: involvement of cholinergic system in skin neuroinflammation?   ScientificWorldJournal . 2008 Feb 6;8: 157-63, Guarneri F, Marini H.

(314) Acute generalized  exanthematous  pustulosis, a clue to neutrophil-mediated inflammatory processes orchestrated by T cells.   Britschgi M, Pichler  WJ,    Curr Opin  Allergy Clin Immunol. 2002 Aug;2(4):325-31;   [ Allergic contact dermatitis][Article in Polish]   Pol  Merkur   Lekarski . 2003, Jun;14(84):605-8.   Gliński  W; & Acute generalized  exanthematous  pustulosis, a clue to neutrophil-mediated inflammatory processes orchestrated by T cells.    Curr   Opin  Allergy Clin Immunol. 2002 Aug;2(4):325-31 Britschgi  M, Pichler WJ; & A case of immediate hypersensitivity reaction associated with an amalgam  restoration,   Kal  BI,  Evcin  O,  Dundar  N, Tezel H,  UnalI .   Br Dent J. 2008 Nov 22;205(10):547-50

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(325) C.R. Adams et al, �Hg & ALS�, JAMA, 1983, 250(5):642-5; & M. Su et  al,      J Neurol Sci, 1998, 156(1):12-7;          & B.  Arvidson (Sweden), Muscle Nerve, 1992,   15(10);1089-94, 

(327) G.  Danscher  et al, Environ Res, �Localization of mercury in the CNS �,        1986, 41:29-43; & Exp Mol  Pathol , 1990, 52: 291-299; & �Ultrastructural         localization of mercury after exposure to mercury vapor�, Prog  Histochem   Cytochem , 1991, 23:249-255.   (rats & primates)

( 329)( a)  Arvidson  B; Arvidsson J; Johansson K, "Mercury Deposits in Neurons of the Trigeminal Ganglia After Insertion of Dental Amalgam in Rats",  Biometals ; 7 (3) p261-263 1994; & (b) Arvidson  B. Inorganic mercury is transported from muscular nerve terminals to spinal and brainstem motor neurons.  Muscle Nerve 1992, 15:1089-94; & B.  Arvidson  et al, Acta Neurol  Scand , �Retrograde axonal transport  of  mercury  in primary sensory neurons� 1990,82:324-237 &  Neurosci  Letters, 1990, 115:29-32; & Arvidson  B, Arvidsson J.  Retrograde axonal transport of mercury in primary sensory neurons innervating the tooth pulp in the rat.   Neurosci  Lett. 1990 Jul 17;115(1):29-32

(334) Univ. of Kentucky Dept. Of Chemistry web page,

(341)  A.Tosti  et al, �Contact stomatitis�, Semin  Cutan  Med Surg, 1997, 16(4):314-9; &  T.Nakada  et al, �Patch test materials for mercury allergic contact dermatitis�, Dermatitis, 1997, 36(5):237-9; & Guttman- Yassky  E,  Weltfriend  S, Bergman R.  Resolution of orofacial granulomatosis with amalgam removal.  J Eur  Acad  Dermatol  Venereol . 2003 May;17(3):344-7; &  Lazarov  A, Kidron D,  Tulchinsky  Z,  Minkow  B. Contact orofacial granulomatosis caused by delayed hypersensitivity to gold and mercury.  J Am  Acad  Dermatol. 2003 Dec;49(6):1117-20. 

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see research web pages on amalgam toxicity, root canals,  cavitations .;  

&(b)  Thomas E. Levy , MD, FACC, and Hal A. Huggins, DDS, MS; Routine Dental Extractions Routinely Produce  Cavitations , Journal of Advancement in Medicine Volume 9, Number 4, Winter 1996 &   ; &

(447) Amalgam/mercury poisoned  patients  organizations, DAMS: Assoc. Of Dental Mercury Patients-U.S.,   ;             

(486) Dr.  Hulda  Clark, The Cure for All Cancers, 1998, ; & Gerson         


 Dr.  Hulda  Clark,  The Cure for all Diseases , New Century Press,2000, (amalgam replacement and treatment for parasites/ bacteria)( U.S. CDC confirms parasites common in those with chronic immune conditions)

(525) Cheshire, William P., Jr. The shocking tooth about trigeminal neuralgia. New England Journal of  Medicine,       Vol. 342, June 29, 2000, p. 2003, &   Bergman M,  Ginstrup  O, Nilsson B. Potentials of and currents between dental metallic restorations.  Scand  J Dent Res  1982;90:404 -8; &  Hugoson  A. Results obtained from patients referred for the investigation of complaints related to oral galvanism.  Swed  Dent J  1986;10:15 -28 & Johann Lechner, "Dental Materials and Psychoneuroimmunology      Conference".  Danderyd  Hospital, 14-16 August,1998;

(530)  Cancer case histories followed by  doctors,

(543) U.S. Centers for Disease Control, National Center for Health  Statistics,  NHANES  III 

study( thousands of people� s health monitored), l ;  &   & Review: cancer related to mercury 

exposure, B. Windham (Ed)     ;  & (b)  Laks , Dan R. Assessment 

of chronic mercury exposure within the U.S. population, National Health and Nutrition 

Examination Survey, 1999�2006.  Biometals . August 2009; &  Laks , D.R. et al, Mercury has 

an affinity for pituitary hormones, Medical Hypotheses, Dec 2009; & (c)  An Investigation of 

Factors Related to Levels of Mercury in Human  Hair,    Environmental Quality Institute, 

October 01, 2005,

(582) Surgical treatment of amalgam fillings causing iatrogenic sinusitis.    Selmani  Z,  Ashammakhi  N.    J  Craniofac  Surg. 2006 Mar;17(2):363- 5;  & (b) Chronic maxillary sinusitis of dental origin and  nasosinusal  aspergillosis.    Fligny  I, Lamas G, Rouhani  FSoudant  J.    Ann  Otolaryngol   Chir   Cervicofac . 1991;108(8):465-8; & (c) Chronic unilateral maxillary sinusitis caused by foreign bodies in the maxillary  sinus,   Tingsgaard  PK, Larsen   PL.    UgeskrLaeger . 1997 Jul 7;159(28):4402-4

(600) B.  Windham,Ed .Anotated  Bibliography: Exposure Levels and Health Effects of Mercury from Amalgam  Fillings and Results of  Filling Replacement, 2000,(over 4000 Medical  Studies & scientific  journal  references and 60,000 clinical cases of replacement followed by doctors),

note:  etc  in a  list  denotes  that author is aware of more references on this subject, generally available in (600).

(601) B.  Windham( Ed), Annotated bibliography: Level of Exposure to mercury from dental amalgam, 2005,

(602) B.  Windham( Ef ), Occupational exposure to mercury in dental staff: exposure levels and effects, 2003,