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26. The C677T MTHFR variant and the risk of venous thrombosis. Salden A; Keeney S; Hay CR; Cumming AM Br J Haematol; 1997 Nov; 99(2):472. PubMed ID: 9375781 [No Abstract] [Full Text] [Related]
27. The homocysteine confusion: now, more is better? Canavese C; Messuerotti A; Fenoglio R; Mesiano P; Massarenti P; Pauletto D; Aimo G; Priolo G Kidney Int; 2002 May; 61(5):1907-8; author reply 1908-9. PubMed ID: 11967046 [No Abstract] [Full Text] [Related]
28. Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan. Gurgey A; Rustemov R; Parlak H; Balta G Thromb Haemost; 1998 Sep; 80(3):520-1. PubMed ID: 9759638 [No Abstract] [Full Text] [Related]
31. Prevalence of the 677C to T mutation in the methylenetetrahydrofolate reductase gene in Italian patients with venous thrombotic disease. De Stefano V; Chiusolo P; Paciaroni K; Serra FG; Voso MT; Casorelli I; Rossi E; Leone G Thromb Haemost; 1998 Mar; 79(3):686-7. PubMed ID: 9531064 [No Abstract] [Full Text] [Related]
32. Hyperhomocysteinaemia in a young woman presenting with stroke, associated with methylene tetrahydrofolate reductase C677T homozygosity. Saldana Chaparro R; Barron JL Ann Clin Biochem; 2004 May; 41(Pt 3):241-4. PubMed ID: 15117441 [TBL] [Abstract][Full Text] [Related]
33. Recurrent coronary events are not increased in postinfarction patients with methylenetetrahydrofolate reductase gene C677T polymorphism. Vulapalli R; Liang C; Zareba W; Moss AJ Am J Cardiol; 2001 Jun; 87(11):1289-92. PubMed ID: 11377358 [No Abstract] [Full Text] [Related]
34. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans]. Guo C; Guo Q; Gong Y; Chen B; Liu Q; Li J; Gao G; Zhou H Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465 [TBL] [Abstract][Full Text] [Related]
35. Reduced frequency of the thermolabile methylenetetrahydrofolate reductase genotype in the elderly. Kluijtmans LA; Whitehead AS Atherosclerosis; 1999 Oct; 146(2):395-7. PubMed ID: 10532696 [No Abstract] [Full Text] [Related]