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264 related items for PubMed ID: 12384649
1. 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 [Abstract] [Full Text] [Related]
2. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients. Gemmati D, Serino ML, Trivellato C, Fiorini S, Scapoli GL. Haematologica; 1999 Sep; 84(9):824-8. PubMed ID: 10477457 [Abstract] [Full Text] [Related]
4. Venous thromboembolic disease and the prothrombin, methylene tetrahydrofolate reductase and factor V genes. Alhenc-Gelas M, Arnaud E, Nicaud V, Aubry ML, Fiessinger JN, Aiach M, Emmerich J. Thromb Haemost; 1999 Apr; 81(4):506-10. PubMed ID: 10235429 [Abstract] [Full Text] [Related]
7. Methylenetetrahydrofolate reductase (MTHFR). Incidence of the C677T mutation in a Siberian female population. Belkovets AV, Kurilovich SA, Agarwal DP. Anthropol Anz; 2001 Mar; 59(1):19-25. PubMed ID: 11360806 [Abstract] [Full Text] [Related]
8. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome. Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ. Am J Hematol; 2002 Sep; 71(1):11-4. PubMed ID: 12221667 [Abstract] [Full Text] [Related]
9. Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population. Ghaznavi H, Soheili Z, Samiei S, Soltanpour MS. Blood Coagul Fibrinolysis; 2015 Dec; 26(8):869-73. PubMed ID: 26083986 [Abstract] [Full Text] [Related]
10. Common C677T polymorphism of the methylenetetrahydrofolate reductase gene and the risk of venous thromboembolism: meta-analysis of 31 studies. Ray JG, Shmorgun D, Chan WS. Pathophysiol Haemost Thromb; 2002 Dec; 32(2):51-8. PubMed ID: 12214149 [Abstract] [Full Text] [Related]
11. Serum homocysteine, thermolabile variant of methylene tetrahydrofolate reductase (MTHFR), and venous thromboembolism: Longitudinal Investigation of Thromboembolism Etiology (LITE). Tsai AW, Cushman M, Tsai MY, Heckbert SR, Rosamond WD, Aleksic N, Yanez ND, Psaty BM, Folsom AR. Am J Hematol; 2003 Mar; 72(3):192-200. PubMed ID: 12605391 [Abstract] [Full Text] [Related]
12. Case-control Study of methylenetetrahydrofolate reductase mutations and hyperhomocysteinemia and risk of stroke. Almawi WY, Khan A, Al-Othman SS, Bakhiet M. J Stroke Cerebrovasc Dis; 2009 Mar; 18(5):407-8. PubMed ID: 19717029 [Abstract] [Full Text] [Related]
13. 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 12; 167(5):497-501. PubMed ID: 17353498 [Abstract] [Full Text] [Related]
15. Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease. Couturaud F, Oger E, Abalain JH, Chenu E, Guias B, Floch HH, Mercier B, Mottier D, Leroyer C. Respiration; 2000 Mar 12; 67(6):657-61. PubMed ID: 11124649 [Abstract] [Full Text] [Related]
16. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism]. Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS. Ter Arkh; 2006 Mar 12; 78(6):70-6. PubMed ID: 16881367 [Abstract] [Full Text] [Related]
18. Protective effect against alcohol dependence of the thermolabile variant of MTHFR. Saffroy R, Benyamina A, Pham P, Marill C, Karila L, Reffas M, Debuire B, Reynaud M, Lemoine A. Drug Alcohol Depend; 2008 Jul 01; 96(1-2):30-6. PubMed ID: 18328637 [Abstract] [Full Text] [Related]
19. Hyperhomocysteinemia and methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations in patients with inflammatory bowel disease. Fernández-Miranda C, Martínez Prieto M, Casis Herce B, Sánchez Gómez F, Gómez González P, Martínez López J, Sáenz-López Pérez S, Gómez de la Cámara A. Rev Esp Enferm Dig; 2005 Jul 01; 97(7):497-504. PubMed ID: 16262529 [Abstract] [Full Text] [Related]