Treatment of erectile dysfunction due to C677T mutation of the MTHFR gene with vitamin B6 and folic acid in patients non responders to PDE5i. J Sex Med 2010; 7:216-223.Lombardo F, Tsamatropoulos P, Piroli E, Culasso F, Jannini EA, Dondero F, Lenzi A, Gandini L. Treatment of ...
MTHFR Doctors provides resources and information on treatments for methylation, DNA, COMT and MTHFR mutation. Genetic home test kits.
The woman was found to be wild type for both MTHFR SNPs with a serum homocysteine 10.5 µM, slightly higher than our accepted normal value of 8.5 µM. The man was found to be a carrier of a triple mutation for 677C < T and 1298 A < C, with an elevated homocysteine ...
Not all MTHFR mutations are similar, and many do not even cause any noticeable side effects. There are two main MTHFR mutations — the C677T and the A1298C mutation. At least one C677T mutation is present in up to 40 percent of Americans. In fact, up to 15 percent of people have ...
C677T mutation in the methylenetetrahydrofolate reductase gene (MTHFR) on the change in plasma homocysteine levels during MTX treatment, and (iii) the ... EAE Van,RFJM Laan,HJ Blom,... - 《Rheumatology》 被引量: 257发表: 2002年 Supplementation with [6S]-5-methyltetrahydrofolate or folic...
L. C. Jordan has acted as a consultant for Berlin Heart. A. E. Hillis declares no competing interests. Rights and permissions Reprints and permissions About this article Cite this article Jordan, L., Hillis, A. Challenges in the diagnosis and treatment of pediatric stroke.Nat Rev Neurol7, ...
C677T polymorphism of the methylenetetrahydrofolate reductase gene is a risk factor of adverse events after coronary revascularization Background: A common point mutation (C677T) in the gene for 5,10-methylenetetrahydrofolate reductase (MTHFR) is associated with hyperhomocysteinemia, an in... N ...
Cui, L. H.et al. Influence of Polymorphisms in Mthfr 677 C–>T, Tyms 3R–>2R and Mtr 2756 a–>G On Nsclc Risk and Response to Platinum-Based Chemotherapy in Advanced Nsclc.Pharmacogenomics12, 797–808 (2011). ArticleCASPubMedGoogle Scholar ...
Role of homocysteine & MTHFR C677T gene polymorphism as risk factors for coronary artery disease in young Indians. Background & objectives: Hyperhomocysteinaemia (HCA) either due to mutation of MTHFR gene or deficiency of vitamin B12 and folic acid, has been reported as... Gupta,S Kumar -...
et al. “Methylenetetrahydrofolate Reductase (MTHFR): The Incidence of Mutations C677T and A1298C in the Ashkenazi Jewish Population” American Journal of Medical Genetics, 1999, pp. 380-384, vol. 86, No. 4. Rao, S. S. C. et al. “Symptoms and stool patterns in patients with ...