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.
110 related articles for article (PubMed ID: 26215413)
21. Impact of thrombogenic mutations on clinical phenotypes of von Willebrand disease. Ahmad F; Kannan M; Yadav V; Biswas A; Saxena R Clin Appl Thromb Hemost; 2010 Jun; 16(3):281-7. PubMed ID: 19959486 [TBL] [Abstract][Full Text] [Related]
22. 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]
23. Frequency of thrombophilic genetic polymorphisms among Saudi subjects compared with other populations. Settin AA; Alghasham A; Ali A; Dowaidar M; Ismail H Hematology; 2012 May; 17(3):176-82. PubMed ID: 22664118 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. The role of FV 1691G>A, FII 20210G>A mutations and MTHFR 677C>T; 1298A>C and 103G>T FXIII gene polymorphisms in pathogenesis of intraventricular hemorrhage in infants born before 32 weeks of gestation. Szpecht D; Gadzinowski J; Seremak-Mrozikiewicz A; Kurzawińska G; Drews K; Szymankiewicz M Childs Nerv Syst; 2017 Jul; 33(7):1201-1208. PubMed ID: 28578513 [TBL] [Abstract][Full Text] [Related]
26. 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]
27. Thrombophilic polymorphisms in Israel. Zoossmann-Diskin A; Gazit E; Peleg L; Shohat M; Turner D Blood Cells Mol Dis; 2008; 41(2):230-3. PubMed ID: 18583164 [TBL] [Abstract][Full Text] [Related]
28. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians. Eid SS; Rihani G Clin Lab Sci; 2004; 17(4):200-2. PubMed ID: 15559724 [TBL] [Abstract][Full Text] [Related]
29. MTHFR polymorphic variant C677T is associated to vascular complications in sickle-cell disease. Hatzlhofer BL; Bezerra MA; Santos MN; Albuquerque DM; Freitas EM; Costa FF; Araújo AS; Muniz MT Genet Test Mol Biomarkers; 2012 Sep; 16(9):1038-43. PubMed ID: 22924497 [TBL] [Abstract][Full Text] [Related]
30. 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]
31. Association of folate metabolism gene polymorphisms and pulmonary embolism: A case-control study of West-Siberian population. Karmadonova NA; Shilova AN; Kozyreva VS; Subbotovskaya AI; Klevanets JE; Karpenko AA Thromb Res; 2015 May; 135(5):788-95. PubMed ID: 25754229 [TBL] [Abstract][Full Text] [Related]
32. Impact of thrombophilic genes mutations on thrombosis risk in Egyptian nonmetastatic cancer patients. Wahba MA; Ismail MA; Saad AA; Habashy DM; Hafeez ZM; Boshnak NH Blood Coagul Fibrinolysis; 2015 Apr; 26(3):309-15. PubMed ID: 25565385 [TBL] [Abstract][Full Text] [Related]
33. Improved real-time multiplex polymerase chain reaction detection of methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms using nearest neighbor model-based probe design. Agarwal RP; Peters SM; Shemirani M; von Ahsen N J Mol Diagn; 2007 Jul; 9(3):345-50. PubMed ID: 17591934 [TBL] [Abstract][Full Text] [Related]
34. [Molecular diagnostic tests for thrombophilia in patients referred to genetic counseling clinic because due to recurrent pregnancy failure. One center's experience]. Pasińska M; Soszyńska K; Runge A; Dabrowska A; Juraszek A; Janiszewska T; Olga H Ginekol Pol; 2012 Mar; 83(3):178-82. PubMed ID: 22568192 [TBL] [Abstract][Full Text] [Related]