555 related articles for article (PubMed ID: 29855758)
1. 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]
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. Evaluation of Factor V Leiden, Prothrombin G20210A, MTHFR C677T and MTHFR A1298C gene polymorphisms in retinopathy of prematurity in a Turkish cohort.
Aydin H; Gunay M; Celik G; Gunay BO; Aydin UT; Karaman A
Ophthalmic Genet; 2016 Dec; 37(4):415-418. PubMed ID: 27018927
[TBL] [Abstract][Full Text] [Related]
4. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
Salimi S; Saravani M; Yaghmaei M; Fazlali Z; Mokhtari M; Naghavi A; Farajian-Mashhadi F
Arch Gynecol Obstet; 2015 Jun; 291(6):1303-12. PubMed ID: 25480409
[TBL] [Abstract][Full Text] [Related]
5. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
Dölek B; Eraslan S; Eroğlu S; Kesim BE; Ulutin T; Yalçiner A; Laleli YR; Gözükirmizi N
Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
[TBL] [Abstract][Full Text] [Related]
6. MTHFR (C677T, A1298C), FV Leiden polymorphisms, and the prothrombin G20210A mutation in arterial ischemic stroke among young tunisian adults.
M'barek L; Sakka S; Meghdiche F; Turki D; Maalla K; Dammak M; Kallel C; Mhiri C
Metab Brain Dis; 2021 Mar; 36(3):421-428. PubMed ID: 33400068
[TBL] [Abstract][Full Text] [Related]
7. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.
Farahmand K; Totonchi M; Hashemi M; Reyhani Sabet F; Kalantari H; Gourabi H; Mohseni Meybodi A
J Matern Fetal Neonatal Med; 2016; 29(8):1269-73. PubMed ID: 26135458
[TBL] [Abstract][Full Text] [Related]
8. Clinical impact of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations among sickle cell disease patients of Central India.
Nishank SS; Singh MP; Yadav R
Eur J Haematol; 2013 Nov; 91(5):462-6. PubMed ID: 23992124
[TBL] [Abstract][Full Text] [Related]
9. Association of MTHFR C677T, MTHFR A1298C, and MTRR A66G Polymorphisms with Neural Tube Defects in Tunisian Parents.
Nasri K; Midani F; Kallel A; Ben Jemaa N; Aloui M; Boulares M; Lassoued M; Ben Halima M; Ben Wafi S; Soussi M; Mahjoubi I; Baara A; Ben Fradj MK; Omar S; Feki M; Jemaa R; Gaigi SS; Marrakchi R
Pathobiology; 2019; 86(4):190-200. PubMed ID: 31238314
[TBL] [Abstract][Full Text] [Related]
10. Deep venous thrombosis and thrombophilic mutations in western Iran: association with factor V Leiden.
Rahimi Z; Mozafari H; Shahriari-Ahmadi A; Alimogaddam K; Ghavamzadeh A; Aznab M; Mansouri K; Rezaei M; Parsian A
Blood Coagul Fibrinolysis; 2010 Jul; 21(5):385-8. PubMed ID: 20479641
[TBL] [Abstract][Full Text] [Related]
11. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
Sadikova ShE; Karimov KhIa; Muminov ShM; Tulakov RP; Boboev KT
Tsitol Genet; 2008; 42(6):50-4. PubMed ID: 19253755
[TBL] [Abstract][Full Text] [Related]
12. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
Toydemir PB; Elhan AH; Tükün A; Toydemir R; Gürler A; Tüzüner A; Bökesoy I
J Rheumatol; 2000 Dec; 27(12):2849-54. PubMed ID: 11128675
[TBL] [Abstract][Full Text] [Related]
13. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
Kader HA; Berman WF; Al-Seraihy AS; Ware RE; Ulshen MH; Treem WR
J Pediatr Gastroenterol Nutr; 2002 Nov; 35(5):629-35. PubMed ID: 12454577
[TBL] [Abstract][Full Text] [Related]
14. Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence.
Simsek E; Yesilyurt A; Pinarli F; Eyerci N; Ulus AT
Gene; 2014 Feb; 536(1):171-6. PubMed ID: 24334115
[TBL] [Abstract][Full Text] [Related]
15. The Contributions of Thrombophilic Mutations to Genetic Susceptibility to Deep Venous Thrombosis in Iraqi Patients.
Al-Allawi NA; Badi AI; Goran MA; Nerweyi FF; Ballo HM; Al-Mzury NT
Genet Test Mol Biomarkers; 2015 Sep; 19(9):500-4. PubMed ID: 26196588
[TBL] [Abstract][Full Text] [Related]
16. Genetic polymorphisms in venous thrombosis and pulmonary embolism after total hip arthroplasty: a pilot study.
Ringwald J; Berger A; Adler W; Kraus C; Pitto RP
Clin Orthop Relat Res; 2009 Jun; 467(6):1507-15. PubMed ID: 18800213
[TBL] [Abstract][Full Text] [Related]
17. Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
Ben Salem-Berrabah O; Fekih-Mrissa N; N'siri B; Ben Hamida A; Benammar-Elgaaied A; Gritli N; Mrissa R
J Clin Neurosci; 2012 Sep; 19(9):1326-7. PubMed ID: 22721898
[TBL] [Abstract][Full Text] [Related]
18. [Study on the association of polymorphisms in homocysteine metabolism related enzymes with deep venous thrombosis].
Yu HD; Zheng H; Qi H; Lian JH; He Y; Dong ZM
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Dec; 23(6):635-9. PubMed ID: 17160942
[TBL] [Abstract][Full Text] [Related]
19. Risk of recurrent venous thrombosis in patients with G20210A mutation in the prothrombin gene or factor V Leiden mutation.
González-Porras JR; García-Sanz R; Alberca I; López ML; Balanzategui A; Gutierrez O; Lozano F; San Miguel J
Blood Coagul Fibrinolysis; 2006 Jan; 17(1):23-8. PubMed ID: 16607075
[TBL] [Abstract][Full Text] [Related]
20. Association between MTHFR polymorphisms (MTHFR C677T, MTHFR A1298C) and recurrent implantation failure: a systematic review and meta-analysis.
Zeng H; He D; Zhao Y; Liu NG; Xie H
Arch Gynecol Obstet; 2021 Apr; 303(4):1089-1098. PubMed ID: 33128585
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
