145 related articles for article (PubMed ID: 25264994)
1. Hereditary Thrombophilic Factors in Glaucoma.
Sekeroglu MA; Irkec M; Mocan MC; Orhan M
J Glaucoma; 2016 Feb; 25(2):203-7. PubMed ID: 25264994
[TBL] [Abstract][Full Text] [Related]
2. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study.
Koylu MT; Kucukevcilioglu M; Erdurman FC; Durukan AH; Sobacı G; Torun D; Tunca Y; Ayyildiz O
Ophthalmic Genet; 2017; 38(4):352-356. PubMed ID: 28085519
[TBL] [Abstract][Full Text] [Related]
3. Plasma homocysteine, MTHFR gene mutation, and open-angle glaucoma.
Clement CI; Goldberg I; Healey PR; Graham SL
J Glaucoma; 2009 Jan; 18(1):73-8. PubMed ID: 19142139
[TBL] [Abstract][Full Text] [Related]
4. Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?
Chatterjee T; Gupta N; Choudhry VP; Behari M; Saxena R; Ashraf MZ
Blood Coagul Fibrinolysis; 2013 Jun; 24(4):449-53. PubMed ID: 23337710
[TBL] [Abstract][Full Text] [Related]
5. Thrombophilia in young patients with acute myocardial infarction.
Celik M; Altintas A; Celik Y; Karabulut A; Ayyildiz O
Saudi Med J; 2008 Jan; 29(1):48-54. PubMed ID: 18176672
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Single and combined prothrombotic factors in patients with idiopathic venous thromboembolism: prevalence and risk assessment.
Salomon O; Steinberg DM; Zivelin A; Gitel S; Dardik R; Rosenberg N; Berliner S; Inbal A; Many A; Lubetsky A; Varon D; Martinowitz U; Seligsohn U
Arterioscler Thromb Vasc Biol; 1999 Mar; 19(3):511-8. PubMed ID: 10073951
[TBL] [Abstract][Full Text] [Related]
8. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
Rahimi Z; Nomani H; Mozafari H; Vaisi-Raygani A; Madani H; Malek-Khosravi S; Parsian A
Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
[TBL] [Abstract][Full Text] [Related]
9. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
Kabukcu S; Keskin N; Keskin A; Atalay E
Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
[TBL] [Abstract][Full Text] [Related]
10. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
Mueller T; Marschon R; Dieplinger B; Haidinger D; Gegenhuber A; Poelz W; Webersinke G; Haltmayer M
J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
[TBL] [Abstract][Full Text] [Related]
11. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
Cadoni G; Scipione S; Rocca B; Agostino S; La Greca C; Bonvissuto D; Paludetti G
Ann Otol Rhinol Laryngol; 2006 Mar; 115(3):195-200. PubMed ID: 16572609
[TBL] [Abstract][Full Text] [Related]
12. Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease.
Almawi WY; Ameen G; Tamim H; Finan RR; Irani-Hakime N
J Thromb Thrombolysis; 2004 Jun; 17(3):199-205. PubMed ID: 15353918
[TBL] [Abstract][Full Text] [Related]
13. Venous Thromboembolism After Knee Arthroscopy in Undiagnosed Familial Thrombophilia.
Jetty V; Glueck CJ; Freiberg RA; Wang P
Orthopedics; 2016 Nov; 39(6):e1052-e1057. PubMed ID: 27459142
[TBL] [Abstract][Full Text] [Related]
14. Thrombophilic gene mutations in cirrhotic patients with portal vein thrombosis.
Erkan O; Bozdayi AM; Disibeyaz S; Oguz D; Ozcan M; Bahar K; Karayalcin S; Ozden A; Bozkaya H; Yurdaydin C; Uzunalimoglu O
Eur J Gastroenterol Hepatol; 2005 Mar; 17(3):339-43. PubMed ID: 15716659
[TBL] [Abstract][Full Text] [Related]
15. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
Yasa MH; Bolaman Z; Yukselen V; Kadikoylu G; Karaoglul AO; Batun S
Hepatogastroenterology; 2007; 54(77):1438-42. PubMed ID: 17708272
[TBL] [Abstract][Full Text] [Related]
16. Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India.
Bhattacharyya M; Makharia G; Kannan M; Ahmed RP; Gupta PK; Saxena R
Am J Clin Pathol; 2004 Jun; 121(6):844-7. PubMed ID: 15198356
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
Cruciani F; Moramarco A; Curto T; Labate A; Recupero V; Conti L; Gandolfo GM; Balacco Gabrieli C
Clin Ter; 2003; 154(5):299-303. PubMed ID: 14994919
[TBL] [Abstract][Full Text] [Related]
19. Thrombophilic mutations in pre-eclampsia and pregnancy-induced hypertension.
Omar SZ; Qvist R; Khaing SL; Muniandy S; Bhalla S
J Obstet Gynaecol Res; 2008 Apr; 34(2):174-8. PubMed ID: 18412778
[TBL] [Abstract][Full Text] [Related]
20. The association of factor V G1961A (factor V Leiden), prothrombin G20210A, MTHFR C677T and PAI-1 4G/5G polymorphisms with recurrent pregnancy loss in Bosnian women.
Jusić A; Balić D; Avdić A; Pođanin M; Balić A
Med Glas (Zenica); 2018 Aug; 15(2):158-163. PubMed ID: 29703881
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
