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.
4. Methylene tetrahydrofolate reductase (MTHFR) 677T-->C mutation and unexplained early pregnancy loss. Grandone E; Margaglione M; Colaizzo D; d'Addedda M; D'Andrea G; Pavone G; Di Minno G Thromb Haemost; 1998 May; 79(5):1056-7. PubMed ID: 9609248 [No Abstract] [Full Text] [Related]
5. The mutation C677T in the methylene tetrahydrofolate reductase gene as a risk factor for myocardial infarction in the Portuguese population. Ferrer-Antunes C; Palmeiro A; Morais J; Lourenço M; Freitas M; Providência L Thromb Haemost; 1998 Sep; 80(3):521-2. PubMed ID: 9759639 [No Abstract] [Full Text] [Related]
6. Mutation in the methylenetetrahydrofolate reductase gene might be a risk factor for cerebrovascular disease in peripartum and under oral contraceptive use. Korn-Lubetzki I; Gillis S; Steiner I Eur Neurol; 2001; 45(3):171-3. PubMed ID: 11306861 [TBL] [Abstract][Full Text] [Related]
7. The relationship between MTHFR genotype, serum homocysteine and folate levels. Ali NS; Powell J; Swaminathan R; Markus HS Biochem Soc Trans; 1997 Aug; 25(3):386S. PubMed ID: 9388616 [No Abstract] [Full Text] [Related]
8. C677T mutation in the methylene tetrahydrofolate reductase gene as a risk factor for venous thrombotic disease in Austrian patients. Seinost G; Renner W; Brodmann M; Winkler M; Köppel H; Pilger E Thromb Res; 2000 Dec; 100(5):405-7. PubMed ID: 11150582 [No Abstract] [Full Text] [Related]
9. Premature closure of foramen ovale and renal vein thrombosis in a stillborn twin homozygous for methylene tetrahydrofolate reductase gene polymorphism: a clinicopathologic case study. Stanek J; Bove KE; Bofinger M; Needham D; Saldana LR; Mutema GK; Meyer R J Perinat Med; 2000; 28(1):61-8. PubMed ID: 10765516 [TBL] [Abstract][Full Text] [Related]
10. Methylene tetrahydrofolate reductase gene and coronary artery disease. Iqbal MP; Frossard PM J Pak Med Assoc; 2003 Jan; 53(1):33-6. PubMed ID: 12666851 [No Abstract] [Full Text] [Related]
11. The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism. Tosetto A; Missiaglia E; Frezzato M; Rodeghiero F Br J Haematol; 1997 Jun; 97(4):804-6. PubMed ID: 9217179 [TBL] [Abstract][Full Text] [Related]
12. The 677C-->T mutation of the methylene-tetrahydrofolate reductase gene in the pathogenesis of osteonecrosis of the femoral head. Zalavras CG; Malizos KN; Dokou E; Vartholomatos G Haematologica; 2002 Jan; 87(1):111-2. PubMed ID: 11801474 [No Abstract] [Full Text] [Related]
13. [Hyperhomocysteinemia and C677T mutation of methylenetetrahydrofolate reductase]. Grasa Ullrich JM; Torres Gómez M; Sánchez Marín B; Calvo Martín MT; García Erce JA; Giralt Raichs M An Med Interna; 2002 May; 19(5):269. PubMed ID: 12108010 [No Abstract] [Full Text] [Related]
14. Molecular biology of 5,10-methylenetetrahydrofolate reductase. Födinger M; Hörl WH; Sunder-Plassmann G J Nephrol; 2000; 13(1):20-33. PubMed ID: 10720211 [TBL] [Abstract][Full Text] [Related]
15. The methylenetetrahydrofolate reductase gene C677T mutant and ischemic stroke in sickle cell disease. Driscoll MC; Prauner R Thromb Haemost; 1999 Dec; 82(6):1780-1. PubMed ID: 10613678 [No Abstract] [Full Text] [Related]
16. Worldwide distribution of a common methylenetetrahydrofolate reductase mutation. Schneider JA; Rees DC; Liu YT; Clegg JB Am J Hum Genet; 1998 May; 62(5):1258-60. PubMed ID: 9545406 [No Abstract] [Full Text] [Related]