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99 related items for PubMed ID: 9843165

  • 1. A mutation in the thrombomodulin gene, 127G to A coding for Ala25Thr, and the risk of myocardial infarction in men.
    Doggen CJ, Kunz G, Rosendaal FR, Lane DA, Vos HL, Stubbs PJ, Manger Cats V, Ireland H.
    Thromb Haemost; 1998 Nov; 80(5):743-8. PubMed ID: 9843165
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  • 4. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke, and venous thrombosis in apparently healthy men.
    Ridker PM, Hennekens CH, Lindpaintner K, Stampfer MJ, Eisenberg PR, Miletich JP.
    N Engl J Med; 1995 Apr 06; 332(14):912-7. PubMed ID: 7877648
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  • 6. A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.
    Norlund L, Holm J, Zöller B, Ohlin AK.
    Thromb Haemost; 1997 Feb 06; 77(2):248-51. PubMed ID: 9157575
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  • 8. Thrombin generation in first-degree relatives of patients with venous thromboembolism who have factor V Leiden. A pilot study.
    Couturaud F, Duchemin J, Leroyer C, Delahousse B, Abgrall JF, Mottier D, Groupe d'Etude de la Thrombose de Bretagne Occidentale (G.E.T.B.O).
    Thromb Haemost; 2008 Jan 06; 99(1):223-8. PubMed ID: 18217158
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  • 9. The frequency of 844ins68 mutation in the cystathionine beta-synthase gene is not increased in patients with venous thrombosis.
    Franco R, Maffei F, Lourenço D, Piccinato C, Morelli V, Thomazini I, Zago M.
    Haematologica; 1998 Nov 06; 83(11):1006-8. PubMed ID: 9864922
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  • 10. A common mutation in the gene for coagulation factor XIII-A (VAL34Leu): a risk factor for primary intracerebral hemorrhage is protective against atherothrombotic diseases.
    Gemmati D, Serino ML, Ongaro A, Tognazzo S, Moratelli S, Resca R, Moretti M, Scapoli GL.
    Am J Hematol; 2001 Jul 06; 67(3):183-8. PubMed ID: 11391716
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  • 11. Factor XIII val34leu and the risk of myocardial infarction.
    Franco RF, Pazin-Filho A, Tavella MH, Simões MV, Marin-Neto JA, Zago MA.
    Haematologica; 2000 Jan 06; 85(1):67-71. PubMed ID: 10629595
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  • 12. 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 06; 85(12):1271-6. PubMed ID: 11114134
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  • 15. Haemostatic gene polymorphisms in young indian asian subjects with acute myocardial infarction.
    Ranjith N, Pegoraro RJ, Rom L.
    Med Sci Monit; 2003 Oct 06; 9(10):CR417-21. PubMed ID: 14523329
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  • 16. Potential thrombophilic mutations/polymorphisms in patients with no flow-limiting stenosis after myocardial infarction.
    French JK, Van de Water NS, Sutton TM, Lund M, Gao W, McDowell J, Liu-Stratton Y, Pohorence J, Szymanski D, Goldschmidt-Clermont P, White HD, Browett PJ, Cooke G.
    Am Heart J; 2003 Jan 06; 145(1):118-24. PubMed ID: 12514663
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  • 17. Genetic variation in the human thrombomodulin promoter locus and prognosis after acute coronary syndrome.
    Ohlin AK, Holm J, Hillarp A.
    Thromb Res; 2004 Jan 06; 113(5):319-26. PubMed ID: 15183044
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  • 18. Variants in the coagulation factor 2 receptor (F2R) gene influence the risk of myocardial infarction in men through an interaction with interleukin 6 serum levels.
    Gigante B, Vikström M, Meuzelaar LS, Chernogubova E, Silveira A, Hooft FV, Hamsten A, de Faire U.
    Thromb Haemost; 2009 May 06; 101(5):943-53. PubMed ID: 19404549
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  • 19. A common polymorphism in the complement factor H gene is associated with increased risk of myocardial infarction: the Rotterdam Study.
    Kardys I, Klaver CC, Despriet DD, Bergen AA, Uitterlinden AG, Hofman A, Oostra BA, Van Duijn CM, de Jong PT, Witteman JC.
    J Am Coll Cardiol; 2006 Apr 18; 47(8):1568-75. PubMed ID: 16630992
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  • 20. Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty.
    Philipp CS, Dilley A, Saidi P, Evatt B, Austin H, Zawadsky J, Harwood D, Ellingsen D, Barnhart E, Phillips DJ, Hooper WC.
    Thromb Haemost; 1998 Dec 18; 80(6):869-73. PubMed ID: 9869151
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