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PUBMED FOR HANDHELDS

Journal Abstract Search

247 related items for PubMed ID: 11583311

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  • 3. Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism--pooled analysis of 8 case-control studies including 2310 cases and 3204 controls. Study Group for Pooled-Analysis in Venous Thromboembolism.
    Emmerich J, Rosendaal FR, Cattaneo M, Margaglione M, De Stefano V, Cumming T, Arruda V, Hillarp A, Reny JL.
    Thromb Haemost; 2001 Sep; 86(3):809-16. PubMed ID: 11583312
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  • 7. Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
    Torres JD, Cardona H, Alvarez L, Cardona-Maya W, Castañeda SA, Quintero-Rivera F, Cadavid A, Bedoya G, Tobón L.
    Am J Hematol; 2006 Dec; 81(12):933-7. PubMed ID: 16917913
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  • 9. Thrombophilia as a multigenic disease.
    Zöller B, García de Frutos P, Hillarp A, Dahlbäck B.
    Haematologica; 1999 Jan; 84(1):59-70. PubMed ID: 10091393
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  • 10. Effects of hereditary and acquired risk factors of venous thrombosis on a thrombin generation-based APC resistance test.
    Curvers J, Thomassen MC, Rimmer J, Hamulyak K, van der Meer J, Tans G, Preston FE, Rosing J.
    Thromb Haemost; 2002 Jul; 88(1):5-11. PubMed ID: 12152677
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  • 11. Intraindividual consistency of the activated protein C resistance phenotype.
    Tosetto A, Simioni M, Madeo D, Rodeghiero F.
    Br J Haematol; 2004 Aug; 126(3):405-9. PubMed ID: 15257714
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  • 12. Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery.
    Wåhlander K, Larson G, Lindahl TL, Andersson C, Frison L, Gustafsson D, Bylock A, Eriksson BI.
    Thromb Haemost; 2002 Apr; 87(4):580-5. PubMed ID: 12008938
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  • 13. Clinical evaluation of a functional prothrombin time-based assay for identification of factor V Leiden carriers in a group of Italian patients with venous thrombosis.
    Gessoni G, Valverde S.
    Blood Coagul Fibrinolysis; 2007 Oct; 18(7):603-10. PubMed ID: 17890946
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  • 16. The prothrombin G20210A mutation is a risk factor for sudden hearing loss in young patients.
    Patscheke JH, Arndt J, Dietz K, Zenner HP, Reuner KH.
    Thromb Haemost; 2001 Oct; 86(4):1118-9. PubMed ID: 11686335
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  • 19. Prothrombin 20210A mutation: a mild risk factor for venous thromboembolism but not for arterial thrombotic disease and pregnancy-related complications in a family study.
    Bank I, Libourel EJ, Middeldorp S, Van Pampus EC, Koopman MM, Hamulyák K, Prins MH, Van Der Meer J, Büller HR.
    Arch Intern Med; 2004 Sep 27; 164(17):1932-7. PubMed ID: 15451770
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  • 20. Phenotypic sensitivity to activated protein C in healthy families: importance of genetic components and environmental factors.
    Taralunga C, Gueguen R, Visvikis S, Regnault V, Sass C, Siest G, Lecompte T, Wahl D.
    Br J Haematol; 2004 Aug 27; 126(3):392-7. PubMed ID: 15257712
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