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Natural Co-Enzyme-Q10

 
$9.10
Sample
q10 photo
10 Count Bottle
250mg Capsules
$54.30
1 Month Supply
30 count bottle 350 mg capsules
60 Count Bottle
250mg Capsules
  • Overview
  • Ingredients
  • Directions
  • Side Effects
Co-Enzyme Q10 (CoQ10) is a compound found naturally in the energy-producing center of the cell known as the mitochondria. Co-Enzyme Q10 is involved in the making of an important molecule known as adenosine triphosphate (ATP). ATP serves as the cell's major energy source and drives a number of biological processes including muscle contraction and the production of protein. Co-Enzyme Q10 also works as an antioxidant.
Co-Enzyme Q10..............................250mg

This product is pure nutrition; no fillers, additives or synthetic chemicals.  

The gelatin capsule complies with the requirements published in:

The United States Pharmacopoeia (USP); XXIV / National Formulary (NF) 19
The European Pharmacopoeia (EP); 3rd Edition

Kosher and Halal certified

Suggested Intake:
Dietary Supplement: 1 Capsule per day.
Theraputic Supplement: 2-10 capsules per day.

Natural Co-Enzyme Q10: Keep in a cool dry place below 75 Degrees Fahrenheit.

In spring, summer and fall Co-Enzyme Q10 should allways be shipped second day and next day air. All Co-Enzyme Q10 is shipped from Georgia, U.S.A.

No side effects in the majority of cases.

Occasional stomach upset, increased energy when taken late in evening, one should consume before 1:00PM

 

 



TumorX BioEnerGenics Co-Enzyme Q10

Co-Enzyme Q10: Squamous cell carcinoma can be reversed and cured using this natural substance. In fact, a deficiency induces cancer and allows viruses that promote cancer inside the human body to go unchecked! 2 Co-Enzyme Q10 is Dose Dependent...1 * Ninety mg of Co-Enzyme Q10 was administered daily for 3 months, 6 of 32 patients had partial cancer regression. * When 300 & 390 mg of Co-Enzyme Q10 were given daily for 4 months, 2 of 2 patients had complete cancer regression. *

In other studies, a 49-year-old patient had complete disappearance of lung-area tumor after 6 months of daily doses of 390mg Co-Enzyme Q10. * A 75-year-old patient had complete remission with no metastasis of single breast cancer after lumpectomy and taking 390 mg Co-Enzyme Q10 daily for 4 months. From our experience, 500-1000mg daily is the ideal dosage to destroy cancer cells inside the human body. The article below discusses the correlation between viruses and cancers as well as how TumorX BioEnerGenics Co-Enzyme Q10 can help you prevent and/or cure cancer in your body. 2

The National Cancer Institute on the Effectiveness of Co-Q10...1 A study conducted in Denmark followed 32 breast cancer patients for 18 months. The disease in these patients had metastasized to other areas of the body. The patients received Co-Q10 in addition to standard therapy. The survival rate of these patients was 100%. Six were shown to have evidence of remission, none of the six showed further signs of metastasis. One of the 6 patients and a new patient were treated for several months with higher doses of Co-Q10. Surgical removal of the primary breast tumor had been performed in these patients with residual cancer cells still remaining. After 3 to 4 months of supplementation with Co-Q10, both patients experienced complete regression of residual breast tumors. All 32 patients from the original study were alive at 24 months of observation. This same report also states evidence that coenzyme Q10 lengthens the survival of patients with pancreatic, lung, rectal, laryngeal, colon, and prostate cancers (this information also exist in peer-reviewed, scientific literature).

Cancer needlessly claims the lives of about 560,000 americans each year!1 This article explores the use of TumorX™ BioEnerGetics CoQ-10™, an immune stimulant that has been proven to defeat cancers.

My intent is to educate, inspire, and show unprecedented hope to you and your loved ones. When the immune system is compromised, gene damaging viruses are able to invade the DNA of healthy cells, thus creating cancerous cells.

Viruses Attack DNA

One largely unspoken cause of cancer is viral related. Viruses attack DNA, which cause the immune system to weaken, thus resulting in different types of cancer.3 Breast4 and prostate5 cancer, two of the most prevalent cancers, are two examples of viral related cancers. In a study of human breast cancer, 38.5% of the cancerous tissues examined contained a rodent-transmitted virus:3 mouse mammary tumor virus.

Viruses have contributed to the world-wide cancer epidemic. Aging and malnutrition weaken the body’s immune system and consequently leave the body vulnerable to harmful viruses. In the U.S., 77% of all cancer patients are 55 years and older.1 As of 2007, there were over 186,000 cases of cancer resulting from malnutrition, and the rates continue to grow!1

Some known viruses that cause cancer include: hepatitis B virus (HBV),1 human immunodeficiency virus (HIV),1 human papilloma virus (HPV),1 and heli­cobacter pylori (H. pylori).1 Studies have shown that 75% of liver cancer is caused by Hepatitis B or C.4 The Epstein Barr virus (EBV) infects more than 90% of the world population.9 EBV has been linked to: breast cancer, gastric cancer, nasopharyngeal carcinoma, lymphomas, Hodgkin’s disease/lymphoma, Non-Hodgkin’s lymphomas, and African Burkitt’s lymphoma.2,9

The fundamental difference between cancerous and non-cancerous cells is that cancerous cells do not respond to adjacent cell commands.6 Cancer is a metabolic parasite which destroys the body’s bio-energy6 and invades functioning organs. BioEnerGetics Q-10™ promotes the body’s creation of bio-energy by rebuilding and repairing the immune system. Co-Enzyme Q10 is required in all human cells, in fact, low blood levels of Co-Enzyme Q10 have been detected in patients with cancer.13

Healthy Immune System Cures Cancer

A study reviewed the relation of Co-Enzyme Q10 to the regression of breast cancer.7,10 When 90 mg of Co-Enzyme Q10 was administered daily for 3 months, 6 of 32 patients had partial cancer regression.7,10 When 300 & 390 mg of Co-Enzyme Q10 were given daily for 4 months, 2 of 2 patients had complete cancer regression.7,10 In other studies, a 49-year-old patient had complete disappearance of lung-area tumor after 6 months of daily doses of 390mg Co-Enzyme Q10.8,10 A 75-year-old patient had complete remission with no metastases of single breast cancer after lumpectomy and taking 390 mg Co-Enzyme Q10 daily8 for 4 months.

The National Cancer Institute peer-reviewed studies & anecdotal evidence10 and reported that patients who supplemented with Co-Q10 outlive the statistical mortality rate for patients with pancreatic, lung, rectal, laryngeal, colon, and prostate cancers.10

Conclusion

Persons with cancer should take a multi-function approach to repairing their body. Using Pancreatic Enzyme Therapy: TumorX™ Formulas (103X, 303X, & 403X) to destroy cancer cells.12 One must detoxify the body (303X) and impart metabolic energy where it is needed. Formula Apoptosis™Full Strength, & Easy Digest are herbal antioxidants that have been proven to destroy cancer cells.11 The addition of Formula Pure Energy ATP™ to the body will convert the poisonous waste of the cancer into energy. And BioEnerGetics Q-10™ is an antioxidant scavenger which stimulates the immune system and helps cells produce energy.

Coenzyme Q10 (CoQ10) is a compound found naturally in the energy-producing center of the cell known as the mitochondria. Co-Enzyme Q10 is involved in the making of an important molecule known as adenosine triphosphate (ATP). ATP serves as the cell's major energy source and drives a number of biological processes including muscle contraction and the production of protein. Co-Enzyme Q10 also works as an antioxidant.

Antioxidants are substances that scavenge free radicals, damaging compounds in the body that alter cell membranes, tamper with DNA, and even cause cell death. Free radicals occur naturally in the body, but environmental toxins (including ultraviolet light, radiation, cigarette smoking, and air pollution) can also increase the number of these damaging particles. Free radicals are believed to contribute to the aging process as well as the development of a number of health problems including heart disease and cancer. Antioxidants such as Co-Enzyme Q10 can neutralize free radicals and may reduce or even help prevent some of the damage they cause.

Uses:

Co-Enzyme Q10 boosts energy, enhances the immune system, and acts as an antioxidant. Clinical research suggests that using coenzyme Q10 supplements alone or in combination with other drug therapies and nutritional supplements may help prevent or treat some of the following conditions:

Heart disease

Researchers believe that the beneficial effect of Co-Enzyme Q10 in the prevention and treatment of heart disease is due to its ability to improve energy production in cells, inhibit blood clot formation, and act as an antioxidant. One important clinical study, for example, found that people who received daily Co-Enzyme Q10 supplements within 3 days of a heart attack were significantly less likely to experience subsequent heart attacks and chest pain. In addition, these same patients were less likely to die of heart disease than those who did not receive the supplements.

Heart failure (HF)

Levels of Co-Enzyme Q10 are low in people with congestive heart failure (HF), a debilitating disease that occurs when the heart is not able to pump blood effectively. This can cause blood to pool in parts of the body, such as the lungs and legs. Information from several clinical studies suggests that Co-Enzyme Q10 supplements help reduce swelling in the legs, enhance breathing by reducing fluid in the lungs, and increase exercise capacity in people with HF. Not all clinical studies agree, however. As a result, some experts conclude that Co-Enzyme Q10 supplements do not contribute any benefit to the usual conventional treatment for HF. More conclusive research will help resolve the debate.

High blood pressure

Several clinical studies involving small numbers of people suggest that Co-Enzyme Q10 may lower blood pressure. However, it may take 4 - 12 weeks before any beneficial effect is observed.

High cholesterol

Levels of Co-Enzyme Q10 tend to be lower in people with high cholesterol compared to healthy individuals of the same age. In addition, certain cholesterol-lowering drugs called statins (such as atorvastatin, cerivastatin, lovastatin, pravastatin, simvastatin) appear to deplete natural levels of Co-Enzyme Q10 in the body. Taking Co-Enzyme Q10 supplements can correct the deficiency caused by statin medications without affecting the medication's positive effects on cholesterol levels.

Diabetes

Co-Enzyme Q10 supplements may improve heart health and blood sugar and help manage high cholesterol and high blood pressure in individuals with diabetes. High blood pressure, high cholesterol, and heart disease are all common problems associated with diabetes. Despite some concern that Co-Enzyme Q10 may cause a sudden and dramatic drop in blood sugar (called hypoglycemia), two recent clinical studies of people with diabetes given Co-Enzyme Q10, 200 mg 2 times daily, showed no hypoglycemic response. If you have diabetes, talk to your doctor or registered dietitian before using Co-Enzyme Q10.

Heart damage caused by chemotherapy

Several clinical studies suggest that Co-Enzyme Q10 may help prevent heart damage caused by certain chemotherapy drugs (namely adriamycin or other athracycline medications). More clinical studies are needed to further evaluate the effectiveness of Co-Enzyme Q10 in preventing heart damage in cancer patients undergoing chemotherapy.

Heart surgery

Clinical research indicates that introducing Co-Enzyme Q10 prior to heart surgery, including bypass surgery and heart transplantation, can reduce damage caused by free radicals, strengthen heart function, and lower the incidence of irregular heart beat (arrhythmias) during the recovery phase.

Breast cancer

Studies of women with breast cancer suggest that Co-Enzyme Q10 supplements (in addition to conventional treatment and a nutritional regimen including other antioxidants and essential fatty acids) may shrink tumors, reduce pain associated with the condition, and cause partial remission in some individuals. It is important to recognize that the beneficial effects these women experienced cannot be attributed to Co-Enzyme Q10 alone. Additional antioxidants used in these studies include vitamins C, E, and selenium.

Periodontal (gum) disease

Gum disease is a widespread problem that is associated with swelling, bleeding, pain, and redness of the gums. Clinical studies have reported that people with gum disease tend to have low levels of Co-Enzyme Q10 in their gums. In a few clinical studies involving small numbers of subjects, Co-Enzyme Q10 supplements caused faster healing and tissue repair. Co-Enzyme Q10 is used in mouth rinse products for this condition. Additional studies in humans are needed to evaluate the effectiveness of Co-Enzyme Q10 when used together with traditional therapy for periodontal disease.

Other

Preliminary clinical studies also suggest that Co-Enzyme Q10 may:

  • Improve immune function in individuals with immune deficiencies (such as acquired immunodeficiency syndrome or AIDS) and chronic infections (such as yeast, bacteria, and viral infections)
  • Increase sperm motility leading to enhanced fertility
  • Be used as part of the treatment for Alzheimer's disease and Parkinson's disease
  • Reduce damage from stroke
  • Boost athletic performance
  • Enhance physical activity in people with fatigue syndromes
  • Improve exercise tolerance in individuals with muscular dystrophy
  • Improve symptoms of tinnitus, or ringing in the ears
  • Be beneficial in cosmetics for healthy skin
  • Delay the aging process and increase longevity

Clinical research in all of these areas is underway to determine whether Co-Enzyme Q10 can be safely and effectively used in people with these health problems and needs.

Dietary Sources:

Primary dietary sources of Co-Enzyme Q10 include oily fish (such as salmon and tuna), organ meats (such as liver), and whole grains. Most individuals obtain sufficient amounts of Co-Enzyme Q10 through a balanced diet, but supplementation may be useful for individuals with particular health conditions (see Uses section) or those taking certain medications (see Interactions section).

Available Forms:

Coenzyme Q10 is available as a supplement in several forms, including soft gel capsules, oral spray, hardshell capsules, and tablets. Co-Enzyme Q10 is also added to various cosmetics.

How to Take It:

Pediatric

Use of coenzyme Q10 in children under 18 years of age is only recommended under the supervision of a health care provider.

Adult

For adults 19 years and older: The recommended dose for Co-Enzyme Q10 supplementation is 30 - 200 mg daily.

Coenzyme Q10 is fat-soluble so should be taken with a meal containing fat for optimal absorption. Also, taking coenzyme Q10 at night may help with the body's ability to use it.

Coenzyme Q10 may be used as an oral mouth rinse for gum disease (periodontal). Rinse with 1 teaspoonful (5 mL), 1 - 2 times daily.

Possible Interactions:

If you are currently being treated with any of the following medications, you should not use Co-Enzyme Q10 without first talking to your health care provider.

Daunorubicin and doxorubicin -- Coenzyme Q10 may help to reduce the toxic effects on the heart caused by daunorubicin (Cerubidin) and doxorubicin (Adriamycin), two chemotherapy medications that are commonly used to treat several kinds of cancer. Always speak to your oncologist before taking antioxidants along with chemotherapy.

Blood pressure medications -- In a clinical study of individuals taking blood pressure medications, including diltiazem (Cardizem), metoprolol (Lopressor or Toprol), enalapril (Vasotec), and nitroglycerin (Nitrostat or Nitrobid), Co-Enzyme Q10 supplementation allowed the individuals to take lower dosages of these drugs. This suggests that Co-Enzyme Q10 may enhance the effectiveness of certain blood pressure medications, but more research is needed to verify these results.

Blood-thinning medications -- There have been reports that coenzyme Q10 may decrease the effectiveness of blood-thinning medications such as warfarin (Coumadin) or clopidigrel (Plavix), leading to the need for increased doses. Therefore, given that this medication must be monitored very closely for maintenance of appropriate levels and steady blood thinning, Co-Enzyme Q10 should be used with warfarin only under careful supervision by your health care provider.

Timolol -- Co-Enzyme Q10 supplementation may reduce the heart-related side effects of timolol drops (Betoptic), a beta-blocker medication used to treat glaucoma, without decreasing the effectiveness of the medication.

Other -- Medications that can lower the levels of coenzyme Q10 in the body include statins for cholesterol , including atorvastatin (Lipitor), lovastatin (Mevacor), pravastatin (Pravachol, and simvastatin (Zocor), fibric acid derivatives for cholesterol, including gemfibrozil (Lopid), beta-blockers for high blood pressure, such as atenolol (Tenormin), labetolol (Normodyne), metoprolol (Lopressor or Toprol), and propranolol (Inderal), and tricyclic antidepressant medications, including amitriptyline (Elavil), doxepin (Sinequan), and imipramine (Tofranil).

Alternative Names (Synonyms):

Co-Enzyme Q10; Co-Q10, Vitamin Q, Tumorx Q10, CoenzymeQ, Co-enzyme Q10, CoQ, CoQ10, , dimethoxy-5 methyl-6-decaprenyl benzoquinone, ubidecarenone, ubiquinone, ubiquinone-10, ubiquinone-Q10, vitamin q10, vitamin Q10,

Supporting Research

Aberg F, Appelkvist EL, Broijersen A, et al. Gemfibrozil-induced decrease in serum ubiquinone and alpha- and gamma-tocopherol levels in men with combined hyperlipidaemia. Eur J Clin Invest. 1998;28:235-242.

Aguilaniu H, Durieux J, Dillin A. Metabolism, ubiquinone synthesis, and longevity. Genes Dev. 2005;19(20):2399-406.

Al-Hasso. Coenzyme Q10: a review. Hosp Pharm. 2001;36(1):51-66.

Alleva R, Scaraarmucci A, Mantera F, Bompandre S, Leoni L, Linarro GP. The protective role of ubiquinol—10 against formation of lipid hydroperoxdes in human seminal fluids. Mol Asp Med. 1997;18:221-228.

Baggio E, Gandini R, Plancher AC, Passeri M, Carmosino G. Italian multicenter study on the safety and efficacy of coenzyme Q10 as adjunctive therapy in heart failure. CoQ10 Drug Surveillance Investigators. Mol Aspects Med. 1994;15(Suppl):s287-294.

Beal MF. Therapeutic effects of coenzyme Q10 in neurodegenerative diseases. Methods Enzymol. 2004;382:473-87.

Belardinelli R, Mucaj A, Lacalaprice F, et al., Coenzyme Q10 and exercise training in chronic heart failure. Eur Heart J. 2006;27(22):2675-81.

Berthold HK, Naini A, Di Mauro S, Hallikainen M, Gylling H, Krone W, Gouni-Berthold I. Effect of ezetimibe and/or simvastatin on coenzyme Q10 levels in plasma: a randomised trial. Drug Saf. 2006;29(8):703-12.

Chello M, Mastroroberto P, Romano R, et al. Protection by coenzyme Q10 from myocardial reperfusion injury during coronary artery bypass grafting. Ann Thorac Surg. 1994;58(5):1427-1432.

Chopra RK, Goldman R, Sinatra ST, Bhagavan HN. Relative bioavailability of coenzyme Q10 formulations in human subjects. Int J Vitam Nutr Res. 1998;68:109-113.

Dhanasekaran M, Ren J. The emerging role of coenzyme Q-10 in aging, neurodegeneration, cardiovascular disease, cancer and diabetes mellitus. Curr Neurovasc Res. 2005;2(5):447-59.

de Bustos F, Molina JA, Jimenez-Jimenz FJ, Garcia-Redondo A, Gomez-Escalonilla C, Porta-Etessam J, et al. Serum levels of coenzyme Q10 in patients with Alzheimer's disease. J Neural Transm. 2000;107(2):233-239.

Eriksson JG. The effects of coenzyme Q10 administration on metabolic control in patients with type 2 diabetes mellitus. Biofactors. 1999;9(2-4):315-318.

Folkers K, Langsjoen P, Nara Y, et al. Biochemical deficiencies of coenzyme Q10 in HIV infection and exploratory treatment. Biochem Biophys Res Commun. 1988;153:888-896.

Hanioka T, Tanaka M, Ojima M, Shizukuishi S, Folkers K. Effect of topical application of coenzyme Q10 on adult periodontitis. Mol Aspects Med. 1994;15 Suppl:s241-248.

Heck AM, DeWitt BA, Lukes AL. Potential interactions between alternative therapies and warfarin. Am J Health-System Pharm. 2000;57(13):1221-1227.

Henriksen J, Andersen CB, Hother-Nielsen O, Vaag A, Mortensen SA, Beck-Nielsen H. Impact of ubiquinone (coenzyme Q10) treatment on glycaemic control, insulin requirement and well-being in patients with type 1 diabetes mellitus. Diabet Med. 1999; 16:312-8.

Human JA, Ubbink JB, Jerling JJ, et al. The effect of simvastatin on the plasma antioxidant concentrations in patients with hypercholesterolemia. Clin Chim Acta. 1997;263(1):67-77.

Iarussi D, Auricchio U, Agretto A, et al. Protective effect of coenzyme Q on anthracylines cardiotoxicity: control study in children with acute lymphoblastic leukemia and non-hodgkin lymphoma. Molec Aspects Med. 1994;15(Suppl):S207-S212.

Jolliet P, Simon N, Barre J, et al. Plasma coenzyme Q10 concentrations in breast cancer: prognosis and therapeutic consequences. Int J Clin Pharmacol Ther. 1998;36:506-509.

Judy WV, Hall JH, Dugan W, et al. Coenzyme Q10 reduction of adriamycin cardiotoxicity. In: Folkes K, Yamamura Y, Eds. Biomedical and clinical aspects of coenzyme Q10, Vol. 4. Amsterdam: Elsevier. 1984:231-241.

Khan M, Gross J, Haupt H, et al., A pilot clinical trial of the effects of coenzyme Q10 on chronic tinnitus aurium. Otolaryngol Head Neck Surg. 2007;136(1):72-7.

Kendler BS. Recent nutritional approaches to prevention and therapy of cardiovascular disease. Prog Cardiovasc Nurs. 1997;12(3):3-23.

Khatta M, Alexander BS, Krichten CM, Fisher ML, Freudenberger R, Robinson SW et al. The effect of conenzyme Q10 in patients with congestive heart failure. Ann Int Med. 2000;132(8):636-640.

Langsjoen P, Langsjoen A. Overview of the use of CoQ10 in cardiovascular disease. BioFactors. 1999;9:273-284.

Langsjoen PH, Langsjoen JO, Langsjoen AM, Lucas LA. Treatment of statin adverse effects with supplemental Coenzyme Q10 and statin drug discontinuation. Biofactors. 2005;25(1-4):147-52.

Langsjoen P, Langsjoen A, Willis R, Folkers K. Treatment of Essential Hypertension with Coenzyme Q10. Molec Aspects Med. 1994;15:s265-s272.

Levy G, Kaufmann P, Buchsbaum R, et al., A two-stage design for a phase II clinical trial of coenzyme Q10 in ALS. Neurology. 2006;66(5):660-3.

Lewin A, Loron M. The effect of coenzyme Q10 on sperm mobility and function. Mol Asp Med. 1997;18:213-219.

Lockwood K, Moesgaard S, Folkers K. Partial and complete regression of breast cancer in patients in relation to dosage of coenzyme Q10. Biochem Biophys Res Commun. 1994;199(3):1504-1508.

Lockwood K, Moesgaard S, Hanioka T, Folkers K. Apparent partial remission of breast cancer in "high risk" patients supplemented with nutritional antioxidants, essential fatty acids, and coenzyme Q10. Mol AspMed. 1994;15 Suppl:s231-s240.

Lockwood K, Moesgaard S, Yamamoto T, Folkers K. Progress in therapy of breast cancer with vitamin Q10 and the regression of metastases. Biochem Biophys Res Commun. 1995;212(1):172-177.

Matthews RT, Yang L, Browne S, Baik M, Beal MF. Coenzyme Q10 administration increases brain mitochondrial concentrations and exerts neuroprotective effects. Proc Natl Acad Sci USA. July 21, 1998; 95:8892-8897.

McCarty MF. Coenzyme Q versus hypertension: does CoQ decrease endothelial superoxide generation? Med Hypotheses. 1999;53:300-304.

McCarty MF. Toward practical prevention of type 2 diabetes. Med Hypotheses. 2000;54(5):786-793.

Miyake Y, Shouza A, Nishikawa M, Yonemoto T, Shimizu H, Omoto S, Hayakawa T, Inada M. Effect of treatment with 3-hydroxy-3methylglutaryl coenzyme A reductase inhibitors on serum coenzyme Q10 in diabetic patients. Arzneimittelforschung. 1999;49(4):324-329.

Mortensen SA, Leth A, Agner E, Rohde M. Dose-related decrease of serum coenzyme Q10 during treatment with HMG-CoA reductase inhibitors. Mol Aspects Med. 1997;18Suppl:S137-S144.

Musumeci O, Naini A, Slonim AE, Skavin N, Hadjigeorgiou GL, Krawiecki N, et al. Familial cerebellar ataxia with muscle coenzyme Q10 deficiency. Neurol. 2001;56(7):849-855.

Niibori K, Yokoyama H, Crestanello JA, Whitman GJ. Acute administration of liposomal coenzyme Q10 increases myocardial tissue levels and improves tolerance to ischemia reperfusion injury. J Surg Res. 1998;79:141-145.

Ostrowski RP. Effect of coenzyme Q(10) on biochemical and morphological changes in experimental ischemia in the rat brain. Brain Res Bull. 2000;53(4):399-407.

Ott BR, Owens NJ. Complementary and alternative medicines for Alzheimer's disease. J Geriatr Psychiatry Neurol. 1998;11:163-173.

Overvad K, Diamant B, Holm L, Holmer G, Mortensen SA, Stender S. Review coenzyme Q10 in health and disease. Eur J Clin Nut. 1999;53:764-770.

Palan PR, Connell K, Ramirez E, Inegbenijie C, Gavara RY, Ouseph JA, Mikhail MS. Effects of menopause and hormone replacement therapy on serum levels of coenzyme Q10 and other lipid-soluble antioxidants. Biofactors. 2005;25(1-4):61-6.

Quinzii CM, Dimauro S, Hirano M. Human coenzyme q(10) deficiency. Neurochem Res. 2007;32(4-5):723-7.

Raitakari OT, McCredie RJ, Witting P, Griffiths KA, Letter J, Sullivan D, Stocker R, Celermajer DS. Coenzyme Q improves LDL resistance to ex vivo oxidation but does not enhance endothelial function in hypercholesterolemic young adults. Free Radic Biol Med. 2000;28(7):1100-1105.

Rosenfeldt F, Hilton D, Pepe S, Krum H. Systematic review of effect of coenzyme Q10 in physical exercise, hypertension and heart failure. Biofactors. 2003;18(1-4):91-100.

Salles JE, Moises VA, Almeida DR, Chacra AR, Moises RS. Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10. Diabetes Res Clin Pract. 2006;72(1):100-3.

Sander S, Coleman CI, Patel AA, Kluger J, White CM. The impact of coenzyme Q10 on systolic function in patients with chronic heart failure. J Card Fail. 2006;12(6):464-72.

Serebruany VL, Ordonez JV, Herzog WR, et al. Dietary coenzyme Q10 supplementation alters platelet size and inhibits human vitronectin (CD51/CD61) receptor expression. J Cardiovasc Pharmacol. 1997;29:16-22.

Shils ME, Olson JA, Shike M, Ross AC. Modern Nutrition in Health and Disease. 9th ed. Baltimore, Md: Williams & Wilkins; 1999:90-92: 1377-1378.

Shinozawa S, Kawasaki H, Gomita Y. [Effect of biological membrane stabilizing drugs (coenzyme Q10, dextran sulfate and reduced glutathione) on adriamycin (doxorubicin)-induced toxicity and microsomal lipid peroxidation in mice]. Gan To Kagaku Ryoho. 1996;23(1):93-98.

Shults CW, Haas R. Clinical trials of coenzyme Q10 in neurological disorders. Biofactors. 2005;25(1-4):117-26.

Shults CW. Therapeutic role of coenzyme Q(10) in Parkinson's disease. Pharmacol Ther. 2005;107(1):120-30.

Sinclair S. Male infertility: nutritional and environmental considerations. Alt Med Rev. 2000;5(1):28-37.

Singh RB, Niaz MA, Rastogi SS, Shukla PK, Thakur AS. Effect of hydrosoluble coenzyme Q10 on blood pressures and insulin resistance in hypertensive patients with coronary artery disease. J Hum Hypertens. 1999;13(3):203-208.

Singh RB, Wander GS, Rastogi A, et al. Randomized, double-blind placebo-controlled trial of coenzyme Q10 in patients with acute myocardial infarction. Cardiovasc Drugs Ther. 1998;12:347-353.

Spigset O. Reduced effect of warfarin caused by ubidecarenone. Lancet. 1994;344:1372-1373.

Takahashi N, Iwasaka T, Sugiura T, et al. Effect of coenzyme Q10 on hemodynamic response to ocular timolol. J Cardiovasc Pharmacol. 1989;14:462-468.

Torkos S. Drug-nutrient interactions: A focus on cholesterol-lowering agents. Int J Integrative Med. 2000;2(3):9-13.

Tsukahara Y, Wakatsuki A, Okatani Y. Antioxidant role of endogenaous coenzyme Q against the iscemic and reperfusion-induced lipid peroxidation in fetal rat brain. Acta Obstet Gynecol Scand. 1999;78(8):669-674.

Weant KA, Smith KM. The role of coenzyme Q10 in heart failure. Ann Pharmacother. 2005;39(9):1522-6.

Wilkinson EG, Arnold RM, Folkers K. Treatment of periodontal and other soft tissue diseases in the oral cavity with coenzyme Q10. In: Folker K, Yamamura Y, eds. Biomedical and Clinical Aspects of Coenzyme Q10, Vol 1. Elsevier/North-Holland Biomedical Press;Amsterdam, 1977:251-265.

Witte KK, Clark AL, Cleland JG. Chronic heart failure and micronutrients. J Am Coll Cardiol. 2001;37(7):1765-1774.

Zhou Q, Chan E. Accuracy of repeated blood sampling in rats: A new technique applied in pharmacokinetic/pharmacodynamic studies of the interaction between warfarin and Co-enzyme Q10. J Pharmacol Toxicol Methods. 1998;40(4):191-199.

 

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