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| Medical Science Journal Reports |
| These journal articles are how research Doctors communicate with each other to share their knowledge gained from experimental successes. They are the gold standard of scientific advance. |
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| Some of the nutraceuticals mentioned in the articles are not ever recommended by Alcoholism Cure. To avoid unwise use by consumers, specific ingredient names have been replaced with (AC). Warnings Our legal advice also supports these disclosure as being helpful for legitimate research doctors and maintaining trade secrets. We are happy to exchange information with legitimate research doctors who agree to protect our rights. |
recently declared superior to most common MD practice.
We have been validated by a $35 million study reports American Journal of Psychiatry
(the most respected independent source of information for MDs who “treat” alcoholism) and Wall
Street Journal on January 3, 2006.
It concluded patient by patient experimentation with a variety of molecules until you
are cured is the best way to work in the pleasure centers of the brain, where alcohol
causes its highs. That is one of the cornerstones of Alcoholism Cure. Contrast our 50
molecules that work in 15 different ways to your MD. He mostly uses 10 that work in
3 ways, and none that permanently cure you.
Such major studies with conclusive results are usually adopted by MDs still in
medical school and by others 5-10 years later.
The study directly applies to prescription antidepressants. These are the only molecules MDs
use to permanently cure alcohol abuse. The cure rate is so bad, and they further damage
your weakened liver, many doctors won’t rely on them. However, even more dramatic, the
logic of the study endorses use of multiple molecule antidepressants that MDs do
not, and our many other non-antidepressants he doesn't even know about.
Especially if you think we are too hard on MDs, look for yourself.
We have been validated by a $35 million study reports American Journal of Psychiatry
(the most respected independent source of information for MDs who “treat” alcoholism) and Wall
Street Journal on January 3, 2006.
It concluded patient by patient experimentation with a variety of molecules until you
are cured is the best way to work in the pleasure centers of the brain, where alcohol
causes its highs. That is one of the cornerstones of Alcoholism Cure. Contrast our 50
molecules that work in 15 different ways to your MD. He mostly uses 10 that work in
3 ways, and none that permanently cure you.
Such major studies with conclusive results are usually adopted by MDs still in
medical school and by others 5-10 years later.
The study directly applies to prescription antidepressants. These are the only molecules MDs
use to permanently cure alcohol abuse. The cure rate is so bad, and they further damage
your weakened liver, many doctors won’t rely on them. However, even more dramatic, the
logic of the study endorses use of multiple molecule antidepressants that MDs do
not, and our many other non-antidepressants he doesn't even know about.
Especially if you think we are too hard on MDs, look for yourself.
| One Traffic Crash Death or DWI is Too Late! JOIN NOW |
Many Pages of Journal Articles Supporting our technology.
Abraham, A.S., Brooks, B.A., and Eyiath, U. 1992. The effects of (AC) supplementation on
serum glucose and lipids in patients with and without non-insulin-dependent diabetes.
Metabolism 41:768-771.
Anderson, R.A., Polansky, M.M. Bryden, N.A., Roginski, E.E.., Mertz, W., and Glinsmann, W.H.
1983. (AC) supplementation of human subjects: effects on glucose, insulin and lipid
parameters. Metabolism 32:894-899.
Anderson, R.A., Bryden, N.A., Polanky, M.M., and Thorp, J.W. 1991a. Effect of carbohydrate
loading and underwater exercise on circulating cortisol, insulin and urinary losses of (AC) and
(AC). Eur. J. Appl. Physiol. 63:146-150.
Anderson, R.A., Polansky, M.M., Bryden, N.A., and Canary, JJ. 199 Ib. Supplemental-(AC)
effects on glucose, insulin, glucagon, and urinary (AC) losses in subjects consuming
controlled low-(AC) diets. Am. J. Clin. Nutr. 54:909-916.
Anderson, R.A. 1997a. Nutritional factors influencing the glucose/insulin system: (AC). J.
Am. Coll. Nutr. 16(5):404-410.
Anderson, R.A., Cheng, N., Bryden, N.A., Polansky, M.M., Cheng, N., Chi, J., and Feng, J.
1997b. Elevated intakes of supplemental (AC) improve glucose and insulin variables in
individuals with type 2 diabetes. Diabetes 46:1786-1791.
Anderson, R.A., Bryden, N.A., and Polansky, M.M. 1997c. Lack of toxicity of (AC) chloride and
(AC) picolinate in rats. J. Am. Coll. Nutr. 16(3):273-279.
Anderson, R.A., Polansky, M.M., Bryden, N.A., Bhathena, S.J., and Canary, J. 1987. Effects of
supplemental (AC) on patients with symptoms of reactive hypoglycemia. Metabolism
36:351-355 (as cited in Anderson 1997).
Anonymous. An adverse reaction to the herbal medication (AC). 1999. Med.J.Aust.
170:218-219.
Bardo, M.T. 1998. Neuropharmacological mechanisms of drug reward: Beyond dopamine in
the nucleus accumbens. Crit. Rev. Neurobiol. 12(1&2):37-67.
Bensky, D. and Gamble, A. (translators). 1993. Chinese Herbal Medicine: Materia Medica. Pp.
47-49.
Bombardelli, E. and Morazzone, P. 1995. (HH). Fitoterapia 66:43-68 (as cited in Josey et al.).
Abraham, A.S., Brooks, B.A., and Eyiath, U. 1992. The effects of (AC) supplementation on
serum glucose and lipids in patients with and without non-insulin-dependent diabetes.
Metabolism 41:768-771.
Anderson, R.A., Polansky, M.M. Bryden, N.A., Roginski, E.E.., Mertz, W., and Glinsmann, W.H.
1983. (AC) supplementation of human subjects: effects on glucose, insulin and lipid
parameters. Metabolism 32:894-899.
Anderson, R.A., Bryden, N.A., Polanky, M.M., and Thorp, J.W. 1991a. Effect of carbohydrate
loading and underwater exercise on circulating cortisol, insulin and urinary losses of (AC) and
(AC). Eur. J. Appl. Physiol. 63:146-150.
Anderson, R.A., Polansky, M.M., Bryden, N.A., and Canary, JJ. 199 Ib. Supplemental-(AC)
effects on glucose, insulin, glucagon, and urinary (AC) losses in subjects consuming
controlled low-(AC) diets. Am. J. Clin. Nutr. 54:909-916.
Anderson, R.A. 1997a. Nutritional factors influencing the glucose/insulin system: (AC). J.
Am. Coll. Nutr. 16(5):404-410.
Anderson, R.A., Cheng, N., Bryden, N.A., Polansky, M.M., Cheng, N., Chi, J., and Feng, J.
1997b. Elevated intakes of supplemental (AC) improve glucose and insulin variables in
individuals with type 2 diabetes. Diabetes 46:1786-1791.
Anderson, R.A., Bryden, N.A., and Polansky, M.M. 1997c. Lack of toxicity of (AC) chloride and
(AC) picolinate in rats. J. Am. Coll. Nutr. 16(3):273-279.
Anderson, R.A., Polansky, M.M., Bryden, N.A., Bhathena, S.J., and Canary, J. 1987. Effects of
supplemental (AC) on patients with symptoms of reactive hypoglycemia. Metabolism
36:351-355 (as cited in Anderson 1997).
Anonymous. An adverse reaction to the herbal medication (AC). 1999. Med.J.Aust.
170:218-219.
Bardo, M.T. 1998. Neuropharmacological mechanisms of drug reward: Beyond dopamine in
the nucleus accumbens. Crit. Rev. Neurobiol. 12(1&2):37-67.
Bensky, D. and Gamble, A. (translators). 1993. Chinese Herbal Medicine: Materia Medica. Pp.
47-49.
Bombardelli, E. and Morazzone, P. 1995. (HH). Fitoterapia 66:43-68 (as cited in Josey et al.).
antidepressant efficacy and adverse effects. J. Clin. Psychopharmacology. 7(3): 127-137.
Clausen, J. 1988. (AC) induced clinical improvement in symptomatic hypoglycemia. Biol.
Trace Elem. Res. 17:229-236.
Cott, J.M. 1997. In vitro receptor binding and enzyme inhibition by (AC) extract.
Pharmacopsychiatry 30(Suppl.2): 108-112 (as cited in Cupp 1999).
Cupp, M.J. 1999. Herbal remedies: Adverse effects and drug interactions. Am. Fam. Phys.
59(5): 1239-1244.
Dahchour, A. and De Witte, P. 2000. Ethanol and amino acids in the central nervous system:
assessment of the pharmacological actions of acamprosate. Prog. Neurobiol.
60(2000):343-362.
Dahchour, A., Durbin, P., De Witte, P. 1995. Ethanol and acamprosate increase the
extracellular (AC) in the nucleus accumbens: a microdialysis study. Alcohol Alcohol. 30:483.
De Mentis, M.G., Olianas, M.C., Haber, B., and Tagliamonte, A. 1978. Increase in large neutral
amino acid transport into brain by insulin. J. Neurochem. 30:121-124.
Elizarova, E.P. and Nedosugova, L.V. 1996. First experiments in (AC) administration for
diabetes mellitus. The effect on erythrocyte membranes. Adv. Exp. Med. Biol. 403:583-8.
Ernst, E., Rand, J.I., Bames, J., and Stevinson, C. 1998. Adverse effects profile of the herbal
antidepressant (AC) L.). Eur. J. Clin. Pharmacol. 54:589-594.
Facts and Comparisons. 1998. The Review of Natural Products. [(AC) monograph].
Feher, J., Lengyel, G., and Blazovics, A. 1998. Oxidative stress in the liver and biliary tract
diseases. Scand. J. Gastroenterol. 33(Suppl.228):38-46.
Flora, K., Hahn, M., Rosen, H., and Benner, K. 1998. (AC) for the therapy of liver disease. Am.
J. Gastroenterol. 93(2): 139-143.
Franconi, F., Bennardini, F., Mattana, A., Miceli, M., Ciuti, M., Mian, M., Gironi, A., Anichini, R.,
Seghieri, G. 1995. Plasma and platelet (AC) are reduced in subjects with insulin-dependent
diabetes mellitus: effects of (AC) supplementation. Am. J. Clin. Nutr. 61(5):1115-9.
Franconi, F., Miceli, M., Fazzini, A., Seghieri, G., Caputo, S., DiLeo, M.A., Lepore, D., Ghirlanda,
G. 1996. (AC) and diabetes. Humans and experimental models. Adv. Exp. Med.Biol.
403:579-82.
Clausen, J. 1988. (AC) induced clinical improvement in symptomatic hypoglycemia. Biol.
Trace Elem. Res. 17:229-236.
Cott, J.M. 1997. In vitro receptor binding and enzyme inhibition by (AC) extract.
Pharmacopsychiatry 30(Suppl.2): 108-112 (as cited in Cupp 1999).
Cupp, M.J. 1999. Herbal remedies: Adverse effects and drug interactions. Am. Fam. Phys.
59(5): 1239-1244.
Dahchour, A. and De Witte, P. 2000. Ethanol and amino acids in the central nervous system:
assessment of the pharmacological actions of acamprosate. Prog. Neurobiol.
60(2000):343-362.
Dahchour, A., Durbin, P., De Witte, P. 1995. Ethanol and acamprosate increase the
extracellular (AC) in the nucleus accumbens: a microdialysis study. Alcohol Alcohol. 30:483.
De Mentis, M.G., Olianas, M.C., Haber, B., and Tagliamonte, A. 1978. Increase in large neutral
amino acid transport into brain by insulin. J. Neurochem. 30:121-124.
Elizarova, E.P. and Nedosugova, L.V. 1996. First experiments in (AC) administration for
diabetes mellitus. The effect on erythrocyte membranes. Adv. Exp. Med. Biol. 403:583-8.
Ernst, E., Rand, J.I., Bames, J., and Stevinson, C. 1998. Adverse effects profile of the herbal
antidepressant (AC) L.). Eur. J. Clin. Pharmacol. 54:589-594.
Facts and Comparisons. 1998. The Review of Natural Products. [(AC) monograph].
Feher, J., Lengyel, G., and Blazovics, A. 1998. Oxidative stress in the liver and biliary tract
diseases. Scand. J. Gastroenterol. 33(Suppl.228):38-46.
Flora, K., Hahn, M., Rosen, H., and Benner, K. 1998. (AC) for the therapy of liver disease. Am.
J. Gastroenterol. 93(2): 139-143.
Franconi, F., Bennardini, F., Mattana, A., Miceli, M., Ciuti, M., Mian, M., Gironi, A., Anichini, R.,
Seghieri, G. 1995. Plasma and platelet (AC) are reduced in subjects with insulin-dependent
diabetes mellitus: effects of (AC) supplementation. Am. J. Clin. Nutr. 61(5):1115-9.
Franconi, F., Miceli, M., Fazzini, A., Seghieri, G., Caputo, S., DiLeo, M.A., Lepore, D., Ghirlanda,
G. 1996. (AC) and diabetes. Humans and experimental models. Adv. Exp. Med.Biol.
403:579-82.
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