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Journal Abstract Search

192 related items for PubMed ID: 10775032

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  • 2. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
    Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.
    Am J Hematol; 2001 Jan; 66(1):28-31. PubMed ID: 11426488
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  • 4. 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
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  • 6. Factor V Leiden and antiphospholipid antibodies are significant risk factors for ischemic stroke in children.
    Kenet G, Sadetzki S, Murad H, Martinowitz U, Rosenberg N, Gitel S, Rechavi G, Inbal A.
    Stroke; 2000 Jun; 31(6):1283-8. PubMed ID: 10835445
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  • 8. Inherited thrombophilia genes in minorities.
    Mack R, Chowdary D, Streck D, Dermody J.
    Genet Test; 1999 Jun; 3(4):371-3. PubMed ID: 10627946
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  • 9. Prevalence of three prothrombotic polymorphisms. Factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase (MTHFR) C 677T in Argentina. On behalf of the Grupo Cooperativo Argentino de Hemostasia y Trombosis.
    Genoud V, Castañon M, Annichino-Bizzacchi J, Korin J, Kordich L.
    Thromb Res; 2000 Nov 01; 100(3):127-31. PubMed ID: 11108898
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  • 10. 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 01; 19(3):189-96. PubMed ID: 16082606
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  • 11. Inherited thrombophilia as a risk factor for the development of ischemic stroke in young adults.
    Voetsch B, Damasceno BP, Camargo EC, Massaro A, Bacheschi LA, Scaff M, Annichino-Bizzacchi JM, Arruda VR.
    Thromb Haemost; 2000 Feb 01; 83(2):229-33. PubMed ID: 10739378
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  • 12. Factor V gene G1691A mutation, prothrombin gene G20210A mutation, and MTHFR gene C677T mutation are not risk factors for pulmonary thromboembolism in Chinese population.
    Lu Y, Zhao Y, Liu G, Wang X, Liu Z, Chen B, Hui R.
    Thromb Res; 2002 Apr 01; 106(1):7-12. PubMed ID: 12165282
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  • 14. Factor V leiden and prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages.
    Foka ZJ, Lambropoulos AF, Saravelos H, Karas GB, Karavida A, Agorastos T, Zournatzi V, Makris PE, Bontis J, Kotsis A.
    Hum Reprod; 2000 Feb 01; 15(2):458-62. PubMed ID: 10655323
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  • 17. Prevalence of genetic markers for thrombophilia in recurrent pregnancy loss.
    Carp H, Salomon O, Seidman D, Dardik R, Rosenberg N, Inbal A.
    Hum Reprod; 2002 Jun 01; 17(6):1633-7. PubMed ID: 12042290
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  • 19. Frequency of factor V, prothrombin and methylenetetrahydrofolate reductase gene variants in preeclampsia.
    D'Elia AV, Driul L, Giacomello R, Colaone R, Fabbro D, Di Leonardo C, Florio P, Petraglia F, Marchesoni D, Damante G.
    Gynecol Obstet Invest; 2002 Jun 01; 53(2):84-7. PubMed ID: 11961379
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  • 20. Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran.
    Rahimi Z, Vaisi-Raygani A, Mozafari H, Kharrazi H, Rezaei M, Nagel RL.
    J Thromb Thrombolysis; 2008 Jun 01; 25(3):280-3. PubMed ID: 17700999
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