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.
5. A common mutation in methylenetetrahydrofolate reductase gene is not a major risk of coronary artery disease or myocardial infarction. Brugada R; Marian AJ Atherosclerosis; 1997 Jan; 128(1):107-12. PubMed ID: 9051203 [TBL] [Abstract][Full Text] [Related]
6. Homocysteine and coronary heart disease: how great is the hazard? Wilson PW JAMA; 2002 Oct 23-30; 288(16):2042-3. PubMed ID: 12387658 [No Abstract] [Full Text] [Related]
7. 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]
10. The TT genotype of the methylenetetrahydrofolate reductase C677T gene polymorphism is associated with the extent of coronary atherosclerosis in patients at high risk for coronary artery disease. Gardemann A; Weidemann H; Philipp M; Katz N; Tillmanns H; Hehrlein FW; Haberbosch W Eur Heart J; 1999 Apr; 20(8):584-92. PubMed ID: 10337543 [TBL] [Abstract][Full Text] [Related]
12. [Genetic polymorphisms of methylenetetrahydrofolate reductase and methionine synthase: association with homocysteine metabolism and late-onset vascular diseases in the Japanese population]. Morita H; Kurihara H; Sugiyama T; Kitamura K; Suzuki S; Sumiyoshi T; Yazaki Y J Cardiol; 1999 Feb; 33(2):106-7. PubMed ID: 10087483 [No Abstract] [Full Text] [Related]
13. MTHFR 677C-->T mutation, folate intake, neural-tube defect, and risk of cardiovascular disease. Wilcken DE Lancet; 1997 Aug; 350(9078):603-4. PubMed ID: 9288038 [No Abstract] [Full Text] [Related]
14. Genetic predisposition to hyperhomocysteinemia: deficiency of methylenetetrahydrofolate reductase (MTHFR). Rozen R Thromb Haemost; 1997 Jul; 78(1):523-6. PubMed ID: 9198208 [No Abstract] [Full Text] [Related]
15. [Relationship between methylenetetrahydrofolate reductase gene polymorphism and coronary heart disease]. Chen B; Wang X; Yu J; Zhang G; Chen F; Den J; Fu S; Li P; Cao W; Yu H Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Oct; 15(5):300-2. PubMed ID: 9758879 [TBL] [Abstract][Full Text] [Related]
16. C677T gene mutation in methylenetetrahydrofolate reductase as a risk factor for cardiac allograft vasculopathy. Elstein E; Huan C; Fitchett D; Cantarovitch M; Marpole D Transplant Proc; 1999; 31(1-2):99. PubMed ID: 10083027 [No Abstract] [Full Text] [Related]
17. Methylenetetrahydrofolate reductase gene and coronary artery disease. van Bockxmeer FM; Mamotte CD; Vasikaran SD; Taylor RR Circulation; 1997 Jan; 95(1):21-3. PubMed ID: 8994411 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Hyperhomocysteinemia, MTHFR C677T genotype and low folate levels: a risk combination for acute coronary disease in a Portuguese population. Araújo F; Lopes M; Gonçalves L; Maciel MJ; Cunha-Ribeiro LM Thromb Haemost; 2000 Mar; 83(3):517-8. PubMed ID: 10744169 [No Abstract] [Full Text] [Related] [Next] [New Search]