133 related articles for article (PubMed ID: 26467879)
1. Methylenetetrahydrofolate Reductase C677T: Hypoplastic Left Heart and Thrombosis.
Spronk KJ; Olivero AD; Haw MP; Vettukattil JJ
World J Pediatr Congenit Heart Surg; 2015 Oct; 6(4):643-5. PubMed ID: 26467879
[TBL] [Abstract][Full Text] [Related]
2. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
Almawi WY; Tamim H; Kreidy R; Timson G; Rahal E; Nabulsi M; Finan RR; Irani-Hakime N
J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
[TBL] [Abstract][Full Text] [Related]
3. Possible Association Between the Methylenetetrahydrofolate Reductase Gene C677T Polymorphism and Preexisting Portal Vein Thrombosis in Liver Transplant Recipients.
Kamei H; Nakamura T; Nagai S; Ishigami M; Hamajima N
Exp Clin Transplant; 2016 Jun; 14(3):313-6. PubMed ID: 27221722
[TBL] [Abstract][Full Text] [Related]
4. [A common mutation C677T in the 5,10-methyltetrahydrofolate reductase gene is associated to idiopathic deep venous thrombosis].
Berrut G; Ghali A; Quere I; Ternisien C; Gallois I; Roy PM; Marre M; Fressinaud P
Rev Med Interne; 2003 Sep; 24(9):569-76. PubMed ID: 12951177
[TBL] [Abstract][Full Text] [Related]
5. Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease.
Junker R; Kotthoff S; Vielhaber H; Halimeh S; Kosch A; Koch HG; Kassenböhmer R; Heineking B; Nowak-Göttl U
Cardiovasc Res; 2001 Aug; 51(2):251-4. PubMed ID: 11470464
[TBL] [Abstract][Full Text] [Related]
6. Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran.
Ehsani M; Imani A; Moravveji A
Mol Biol Rep; 2018 Aug; 45(4):621-624. PubMed ID: 29855758
[TBL] [Abstract][Full Text] [Related]
7. [The C677T mutation in the methylenetetrahydrofolate reductase gene and its association with deep vein thrombophilia in Shandong Hans].
Guo C; Guo Q; Gong Y; Chen B; Liu Q; Li J; Gao G; Zhou H
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Aug; 19(4):295-7. PubMed ID: 12170465
[TBL] [Abstract][Full Text] [Related]
8. Recurrent cerebral venous thrombosis associated with heterozygote methylenetetrahydrofolate reductase C677T mutation and sickle cell trait without homocysteinemia: an autopsy case report and review of literature.
Ali Z; Troncoso JC; Fowler DR
Forensic Sci Int; 2014 Sep; 242():e52-e55. PubMed ID: 25074331
[TBL] [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
[TBL] [Abstract][Full Text] [Related]
10. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
D'Angelo A; Coppola A; Madonna P; Fermo I; Pagano A; Mazzola G; Galli L; Cerbone AM
Thromb Haemost; 2000 Apr; 83(4):563-70. PubMed ID: 10780318
[TBL] [Abstract][Full Text] [Related]
11. Frequency of prothrombotic risk factors in patients with deep venous thrombosis and controls: their implications for thrombophilia screening in Chilean subjects.
Guzmán N; Salazar LA
Genet Test Mol Biomarkers; 2010 Oct; 14(5):599-602. PubMed ID: 20707729
[TBL] [Abstract][Full Text] [Related]
12. MTHFR C677T mutations in liver cirrhosis with and without portal vein thrombosis.
Pasta L; Marrone C; D'amico M; Virdone R; D'amico G; Sammarco P; Fabiano C; Pagliaro L
Liver Int; 2006 Mar; 26(2):269-70. PubMed ID: 16448467
[No Abstract] [Full Text] [Related]
13. 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]
14. Hyperhomocysteinemia and the methylene tetrahydrofolate reductase C677T mutation in splanchnic vein thrombosis.
Vayá A; Plumé G; Bonet E; Carrasco P; Morales-Suárez-Varela MM
Eur J Haematol; 2011 Feb; 86(2):167-72. PubMed ID: 21070369
[TBL] [Abstract][Full Text] [Related]
15. Splenic thrombosis in three patients with moderate hyperhomocysteinemia, low folate and the C677T variant of the methylenetetrahydrofolate reductase (MTHFR) gene.
Starakis I; Mougiou A; Leonidou L; Siagris D; Karatza C
Thromb Haemost; 2005 Dec; 94(6):1333-4. PubMed ID: 16411416
[No Abstract] [Full Text] [Related]
16. The methylenetetrahydrofolate reductase C677T gene mutation is associated with hyperhomocysteinemia, cardiovascular disease and plasma B-type natriuretic peptide levels in Korea.
Cho SE; Hong KS; Shin GJ; Chung WS
Clin Chem Lab Med; 2006; 44(9):1070-5. PubMed ID: 16958597
[TBL] [Abstract][Full Text] [Related]
17. Methylenetetrahydrofolate reductase (MTHFR-677 and MTHFR-1298) genotypes and haplotypes and plasma homocysteine levels in patients with occlusive artery disease and deep venous thrombosis.
Spiroski I; Kedev S; Antov S; Arsov T; Krstevska M; Dzhekova-Stojkova S; Bosilkova G; Kostovska S; Trajkov D; Petlichkovski A; Strezova A; Efinska-Mladenovska O; Spiroski M
Acta Biochim Pol; 2008; 55(3):587-94. PubMed ID: 18800176
[TBL] [Abstract][Full Text] [Related]
18. 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
[TBL] [Abstract][Full Text] [Related]
19. Methylenetetrahydrofolate reductase (MTHFR) C677T polymorphism: epidemiology, metabolism and the associated diseases.
Liew SC; Gupta ED
Eur J Med Genet; 2015 Jan; 58(1):1-10. PubMed ID: 25449138
[TBL] [Abstract][Full Text] [Related]
20. C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.
Erdogan MO; Yildiz SH; Solak M; Eser O; Cosar E; Eser B; Koken R; Buyukbas S
Genet Mol Res; 2010 Jun; 9(2):1197-203. PubMed ID: 20589617
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]