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Journal Abstract Search

609 related items for PubMed ID: 10073951

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  • 4. Prospective evaluation of the thrombotic risk in children with acute lymphoblastic leukemia carrying the MTHFR TT 677 genotype, the prothrombin G20210A variant, and further prothrombotic risk factors.
    Nowak-Göttl U, Wermes C, Junker R, Koch HG, Schobess R, Fleischhack G, Schwabe D, Ehrenforth S.
    Blood; 1999 Mar 01; 93(5):1595-9. PubMed ID: 10029588
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  • 6. 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 01; 41(5):808-15. PubMed ID: 15886665
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  • 7. Methylenetetrahydrofolate reductase C677T genotype and venous thromboembolic disease.
    Couturaud F, Oger E, Abalain JH, Chenu E, Guias B, Floch HH, Mercier B, Mottier D, Leroyer C.
    Respiration; 2000 May 01; 67(6):657-61. PubMed ID: 11124649
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  • 8. Impact of environmental and hereditary risk factors on the clinical manifestation of thrombophilia in homozygous carriers of factor V:G1691A.
    Ehrenforth S, Nemes L, Mannhalter C, Rosendaal FR, Koder S, Zoghlami-Rintelen C, Scharrer I, Pabinger I.
    J Thromb Haemost; 2004 Mar 01; 2(3):430-6. PubMed ID: 15009459
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  • 13. 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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  • 14. 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 01; 91(5):462-6. PubMed ID: 23992124
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  • 15. Prothrombin and factor V mutations in women with a history of thrombosis during pregnancy and the puerperium.
    Gerhardt A, Scharf RE, Beckmann MW, Struve S, Bender HG, Pillny M, Sandmann W, Zotz RB.
    N Engl J Med; 2000 Feb 10; 342(6):374-80. PubMed ID: 10666427
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  • 16. 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 10; 14(5):599-602. PubMed ID: 20707729
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  • 17. Prothrombotic risk factors in children with spontaneous venous thrombosis and their asymptomatic parents: a family study.
    Kosch A, Junker R, Kurnik K, Schobess R, Günther G, Koch H, Nowak-Göttl U.
    Thromb Res; 2000 Sep 15; 99(6):531-7. PubMed ID: 10974337
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  • 18. 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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