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22. Mutations in the gene for methylenetetrahydrofolate reductase, homocysteine levels, and vitamin status in women with a history of preeclampsia. Lachmeijer AM; Arngrímsson R; Bastiaans EJ; Pals G; ten Kate LP; de Vries JI; Kostense PJ; Aarnoudse JG; Dekker GA Am J Obstet Gynecol; 2001 Feb; 184(3):394-402. PubMed ID: 11228493 [TBL] [Abstract][Full Text] [Related]
23. Genetic causes of mild hyperhomocysteinemia in patients with premature occlusive coronary artery diseases. Tsai MY; Welge BG; Hanson NQ; Bignell MK; Vessey J; Schwichtenberg K; Yang F; Bullemer FE; Rasmussen R; Graham KJ Atherosclerosis; 1999 Mar; 143(1):163-70. PubMed ID: 10208491 [TBL] [Abstract][Full Text] [Related]
24. [Prevalence of factor V Leiden, hyperhomocysteinemia, prothrombin G20210A, and methylene tetrahydrofolate reductase C677T mutations in obstetrical complications]. Verdy E; Berkane N; Magdelaine A; Soubrier F; Uzan S Ann Biol Clin (Paris); 1999; 57(5):539-44. PubMed ID: 10518055 [TBL] [Abstract][Full Text] [Related]
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26. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis. Brattström L; Wilcken DE; Ohrvik J; Brudin L Circulation; 1998 Dec; 98(23):2520-6. PubMed ID: 9843457 [TBL] [Abstract][Full Text] [Related]
28. Homocysteine, folate enzymes and neural tube defects. Molloy AM; Weir DG; Scott JM Haematologica; 1999 Jun; 84 Suppl EHA-4():53-6. PubMed ID: 10907468 [No Abstract] [Full Text] [Related]
29. Thrombophilia and adverse pregnancy outcome. Brenner B; Aharon A Clin Perinatol; 2007 Dec; 34(4):527-41, v. PubMed ID: 18063103 [TBL] [Abstract][Full Text] [Related]
30. Hyperhomocysteinemia in hemodialysis patients: effects of 12-month supplementation with hydrosoluble vitamins. Tremblay R; Bonnardeaux A; Geadah D; Busque L; Lebrun M; Ouimet D; Leblanc M Kidney Int; 2000 Aug; 58(2):851-8. PubMed ID: 10916110 [TBL] [Abstract][Full Text] [Related]
31. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease. Kadziela J; Janas J; Dzielińska Z; Szperl M; Gaździk D; Chotkowska E; Piotrowski W; Ruzyłło W Kardiol Pol; 2003 Jul; 59(7):17-26; discussion 26. PubMed ID: 14560345 [TBL] [Abstract][Full Text] [Related]
32. Hyperhomocysteinemia in high-aged subjects: relation of B-vitamins, folic acid, renal function and the methylenetetrahydrofolate reductase mutation. Herrmann W; Quast S; Ullrich M; Schultze H; Bodis M; Geisel J Atherosclerosis; 1999 May; 144(1):91-101. PubMed ID: 10381282 [TBL] [Abstract][Full Text] [Related]
33. Combined heterozygosity for methylenetetrahydrofolate reductase (MTHFR) mutations C677T and A1298C is associated with abruptio placentae but not with intrauterine growth restriction. Gebhardt GS; Scholtz CL; Hillermann R; Odendaal HJ Eur J Obstet Gynecol Reprod Biol; 2001 Aug; 97(2):174-7. PubMed ID: 11451544 [TBL] [Abstract][Full Text] [Related]
34. Plasma homocysteine levels related to interactions between folate status and methylenetetrahydrofolate reductase: a study in 52 healthy subjects. Zittoun J; Tonetti C; Bories D; Pignon JM; Tulliez M Metabolism; 1998 Nov; 47(11):1413-8. PubMed ID: 9826223 [TBL] [Abstract][Full Text] [Related]