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Journal Abstract Search

189 related items for PubMed ID: 10904101

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  • 3. Factor II G20210A and factor V G1691A gene mutations and peripheral arterial occlusive disease.
    Renner W, Köppel H, Brodmann M, Pabst E, Schallmoser K, Toplak H, Wascher TC, Pilger E.
    Thromb Haemost; 2000 Jan; 83(1):20-2. PubMed ID: 10669148
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  • 5. Risk of venous thrombosis in carriers of the prothrombin G20210A variant and factor V Leiden and their interaction with oral contraceptives.
    Aznar J, Vayá A, Estellés A, Mira Y, Seguí R, Villa P, Ferrando F, Falcó C, Corella D, España F.
    Haematologica; 2000 Dec; 85(12):1271-6. PubMed ID: 11114134
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  • 6. [Factor V Leiden (G1691A) and prothrombin-G20210A alleles among patients with deep venous thrombosis and in the general population from Spain].
    Francès F, Portolès O, Gabriel F, Corella D, Sorlí JV, Sabater A, Alfonso JL, Guillén M.
    Rev Med Chil; 2006 Jan; 134(1):13-20. PubMed ID: 16532157
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  • 7. Combined carrier status of prothrombin 20210A and factor XIII-A Leu34 alleles as a strong risk factor for myocardial infarction: evidence of a gene-gene interaction.
    Butt C, Zheng H, Randell E, Robb D, Parfrey P, Xie YG.
    Blood; 2003 Apr 15; 101(8):3037-41. PubMed ID: 12480694
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  • 8. Prevalence of factor V Leiden and prothrombin 20210 A variant in Bulgarian patients with pulmonary thromboembolism and deep venous thrombosis.
    Boyanovsky B, Russeva M, Ganev V, Penev M, Baleva M.
    Blood Coagul Fibrinolysis; 2001 Dec 15; 12(8):639-42. PubMed ID: 11734663
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  • 9. Factor V gene (1691A and 4070G) and prothrombin gene 20210A mutations in patients with Behçet's disease.
    Ateş A, Düzgün N, Ulu A, Tiryaki AO, Akar N.
    Pathophysiol Haemost Thromb; 2003 Dec 15; 33(3):157-63. PubMed ID: 15170396
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  • 11. Paternal endothelial protein C receptor 219Gly variant as a mild and limited risk factor for deep vein thrombosis during pregnancy.
    Galanaud JP, Cochery-Nouvellon E, Alonso S, Chauleur C, Mercier E, Lissalde-Lavigne G, Fabbro-Peray P, Reny JL, Mares P, Dauzat M, Quere I, Gris JC.
    J Thromb Haemost; 2010 Apr 15; 8(4):707-13. PubMed ID: 20141580
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  • 12. [Mutation frequencies of the thrombophilic state genes in Uzbekistan].
    Sadikova ShE, Karimov KhIa, Muminov ShM, Tulakov RP, Boboev KT.
    Tsitol Genet; 2008 Apr 15; 42(6):50-4. PubMed ID: 19253755
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  • 13. The G20210A mutation of the prothrombin gene in patients with previous first episodes of deep-vein thrombosis: prevalence and association with factor V G1691A, methylenetetrahydrofolate reductase C677T and plasma prothrombin levels.
    Cattaneo M, Chantarangkul V, Taioli E, Santos JH, Tagliabue L.
    Thromb Res; 1999 Jan 01; 93(1):1-8. PubMed ID: 10065893
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  • 14. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
    Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.
    Haematologica; 2008 May 01; 93(5):729-34. PubMed ID: 18387978
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  • 15. 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 01; 86(3):809-16. PubMed ID: 11583312
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  • 16. Prevalence of factor V Leiden, FII G20210A, FXIII Val34Leu and MTHFR C677T polymorphisms in cancer patients with and without venous thrombosis.
    Ramacciotti E, Wolosker N, Puech-Leao P, Zeratti EA, Gusson PR, del Giglio A, Franco RF.
    Thromb Res; 2003 Feb 15; 109(4):171-4. PubMed ID: 12757770
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  • 17. [Prevalence of Factor V Leiden and the G20210A mutation of the prothrombin gene in a random group of patients with thrombotic episodes].
    Alvarez A, Barroso A, Robledo M, Arranz E, Outeiriño J, Benítez J.
    Sangre (Barc); 1999 Feb 15; 44(1):7-12. PubMed ID: 10323090
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  • 18. 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 15; 19(3):189-96. PubMed ID: 16082606
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  • 19. Association of a common polymorphism in the factor XIII gene with venous thrombosis.
    Catto AJ, Kohler HP, Coore J, Mansfield MW, Stickland MH, Grant PJ.
    Blood; 1999 Feb 01; 93(3):906-8. PubMed ID: 9920839
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  • 20. The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and the G20210A prothrombin mutation.
    De Stefano V, Martinelli I, Mannucci PM, Paciaroni K, Chiusolo P, Casorelli I, Rossi E, Leone G.
    N Engl J Med; 1999 Sep 09; 341(11):801-6. PubMed ID: 10477778
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