These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
655 related articles for article (PubMed ID: 19717029)
21. Common genetic markers and prediction of recurrent events after ischemic stroke in young adults. Pezzini A; Grassi M; Del Zotto E; Lodigiani C; Ferrazzi P; Spalloni A; Patella R; Giossi A; Volonghi I; Iacoviello L; Magoni M; Rota LL; Rasura M; Padovani A Neurology; 2009 Sep; 73(9):717-23. PubMed ID: 19720979 [TBL] [Abstract][Full Text] [Related]
22. No interaction between factor V Leiden and hyperhomocysteinemia or MTHFR 677TT genotype in venous thrombosis. Results of a meta-analysis of published studies and a large case-only study. Keijzer MB; Borm GF; Blom HJ; Bos GM; Rosendaal FR; den Heijer M Thromb Haemost; 2007 Jan; 97(1):32-7. PubMed ID: 17200768 [TBL] [Abstract][Full Text] [Related]
23. Hyperhomocysteinemia and polymorphisms of the methylenetetrahydrofolate gene in hemodialysis and peritoneal dialysis patients. Domenici FA; Vannucchi MT; Simões-Ambrósio LM; Vannucchi H Mol Nutr Food Res; 2007 Nov; 51(11):1430-6. PubMed ID: 17966140 [TBL] [Abstract][Full Text] [Related]
24. MTHFR C677T mutation in central retinal vein occlusion: a case-control study in Chinese population. Gao W; Wang YS; Zhang P; Wang HY Thromb Res; 2008; 121(5):699-703. PubMed ID: 17719079 [TBL] [Abstract][Full Text] [Related]
25. Methylenetetrahydrofolate reductase C677T polymorphism and Factor V Leiden variant in Mexican women with preeclampsia/eclampsia. Dávalos IP; Moran MC; Martínez-Abundis E; González-Ortiz M; Flores-Martínez SE; Machorro V; Sandoval L; Figuera LE; Mena JP; Oliva JM; Tlacuilo-Parra JA; Sánchez-Corona J; Salazar-Páramo M Blood Cells Mol Dis; 2005; 35(1):66-9. PubMed ID: 15905108 [TBL] [Abstract][Full Text] [Related]
26. Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease. Kerkeni M; Addad F; Chauffert M; Myara A; Gerhardt M; Chevenne D; Trivin F; Farhat MB; Miled A; Maaroufi K Ann Clin Biochem; 2006 May; 43(Pt 3):200-6. PubMed ID: 16704755 [TBL] [Abstract][Full Text] [Related]
27. Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children. Aléssio AC; Höehr NF; Siqueira LH; Bydlowski SP; Annichino-Bizzacchi JM Thromb Res; 2007; 119(5):571-7. PubMed ID: 16820193 [TBL] [Abstract][Full Text] [Related]
28. Lack of association between the C677T mutation in the 5,10-methylenetetrahydrofolate reductase gene and venous thromboembolism in Northwestern Greece. Zalavras ChG; Giotopoulou S; Dokou E; Mitsis M; Ioannou HV; Tzolou A; Kolaitis N; Vartholomatos G Int Angiol; 2002 Sep; 21(3):268-71. PubMed ID: 12384649 [TBL] [Abstract][Full Text] [Related]
29. Association of MTHFR A1298C polymorphism (but not of MTHFR C677T) with elevated homocysteine levels and placental vasculopathies. Klai S; Fekih-Mrissa N; El Housaini S; Kaabechi N; Nsiri B; Rachdi R; Gritli N Blood Coagul Fibrinolysis; 2011 Jul; 22(5):374-8. PubMed ID: 21577095 [TBL] [Abstract][Full Text] [Related]
30. Intermediate and severe hyperhomocysteinemia with thrombosis: a study of genetic determinants. Gaustadnes M; Rüdiger N; Rasmussen K; Ingerslev J Thromb Haemost; 2000 Apr; 83(4):554-8. PubMed ID: 10780316 [TBL] [Abstract][Full Text] [Related]
31. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients. Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197 [TBL] [Abstract][Full Text] [Related]
32. No association between the common MTHFR 677C->T polymorphism and venous thrombosis: results from the MEGA study. Bezemer ID; Doggen CJ; Vos HL; Rosendaal FR Arch Intern Med; 2007 Mar; 167(5):497-501. PubMed ID: 17353498 [TBL] [Abstract][Full Text] [Related]
33. Evaluation of the interactions of common genetic mutations in stroke subtypes. Szolnoki Z; Somogyvári F; Kondacs A; Szabó M; Fodor L J Neurol; 2002 Oct; 249(10):1391-7. PubMed ID: 12382154 [TBL] [Abstract][Full Text] [Related]
34. Hyperhomocysteinemia, C677T MTHFR polymorphism and ischemic stroke in Tunisian patients. Salem-Berrabah OB; Mrissa R; Machghoul S; Hamida AB; N'siri B; Mazigh C; Aouni Z; Louati I; Layouni S; El Oudi M; Fekih-Mrissa N; Gritli N Tunis Med; 2010 Sep; 88(9):655-9. PubMed ID: 20812180 [TBL] [Abstract][Full Text] [Related]
36. The common mutations C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients. Haviv YS; Shpichinetsky V; Goldschmidt N; Atta IA; Ben-Yehuda A; Friedman G Nephron; 2002 Sep; 92(1):120-6. PubMed ID: 12187094 [TBL] [Abstract][Full Text] [Related]
37. The coagulation factor V Leiden, MTHFRC677T variant and eNOS 4ab polymorphism in young Chinese population with ischemic stroke. Shi C; Kang X; Wang Y; Zhou Y Clin Chim Acta; 2008 Oct; 396(1-2):7-9. PubMed ID: 18602910 [TBL] [Abstract][Full Text] [Related]
38. Methylenetetrahydrofolate reductase gene polymorphisms in essential hypertension relation: with the development of hypertensive end-stage renal disease. Tylicki L; Födinger M; Puttinger H; Rutkowski P; Strozecki P; Tyszko S; Rutkowski B; Hörl WH Am J Hypertens; 2005 Nov; 18(11):1442-8. PubMed ID: 16280279 [TBL] [Abstract][Full Text] [Related]
39. Mild hyperhomocysteinemia, C677T polymorphism on methylenetetrahydrofolate reductase gene and the risk of macroangiopathy in type 2 diabetes: a prospective study. Russo GT; Di Benedetto A; Magazzù D; Giandalia A; Giorda CB; Ientile R; Previti M; Di Cesare E; Cucinotta D Acta Diabetol; 2011 Jun; 48(2):95-101. PubMed ID: 19937354 [TBL] [Abstract][Full Text] [Related]
40. Two cousins with neonatal stroke, PAI-1 4G variant and MTHFR A1298C mutation. Golomb MR; Heiny M; Garg BP J Child Neurol; 2007 Jun; 22(6):753-5. PubMed ID: 17641264 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]