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114 related items for PubMed ID: 14523329

  • 1. Haemostatic gene polymorphisms in young indian asian subjects with acute myocardial infarction.
    Ranjith N, Pegoraro RJ, Rom L.
    Med Sci Monit; 2003 Oct; 9(10):CR417-21. PubMed ID: 14523329
    [Abstract] [Full Text] [Related]

  • 2. Synergistic effect of thrombomodulin promoter -33G/A polymorphism and smoking on the onset of acute myocardial infarction.
    Li YH, Chen JH, Tsai WC, Chao TH, Guo HR, Tsai LM, Wu HL, Shi GY.
    Thromb Haemost; 2002 Jan; 87(1):86-91. PubMed ID: 11848462
    [Abstract] [Full Text] [Related]

  • 3. Genetic risk factors in myocardial infarction at young age.
    Incalcaterra E, Hoffmann E, Averna MR, Caimi G.
    Minerva Cardioangiol; 2004 Aug; 52(4):287-312. PubMed ID: 15284679
    [Abstract] [Full Text] [Related]

  • 4. 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; 93(5):729-34. PubMed ID: 18387978
    [Abstract] [Full Text] [Related]

  • 5. 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; 145(1):118-24. PubMed ID: 12514663
    [Abstract] [Full Text] [Related]

  • 6. Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis.
    Silingardi M, Salvarani C, Boiardi L, Accardo P, Iorio A, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Ciccia F, Ghirarduzzi A, Filippini D, Paolazzi G, Iori I.
    Arthritis Rheum; 2004 Apr 15; 51(2):177-83. PubMed ID: 15077257
    [Abstract] [Full Text] [Related]

  • 7. Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction.
    Motovska Z, Kvasnicka J, Widimsky P, Petr R, Hajkova J, Bobcikova P, Osmancik P, Odvodyova D, Katina S.
    Thromb Res; 2010 Feb 15; 125(2):e61-4. PubMed ID: 19786296
    [Abstract] [Full Text] [Related]

  • 8. Age as a risk factor for myocardial infarction in Leiden mutation carriers.
    Baranovskaya S, Kudinov S, Fomicheva E, Vasina V, Solovieva D, Khavinson V, Schwartz E.
    Mol Genet Metab; 1998 Jun 15; 64(2):155-7. PubMed ID: 9705241
    [Abstract] [Full Text] [Related]

  • 9. Coagulation gene polymorphisms as risk factors for myocardial infarction in young Indian Asians.
    Pegoraro RJ, Ranjith N, Rom L.
    Cardiovasc J S Afr; 2005 Jun 15; 16(3):152-7. PubMed ID: 16049588
    [Abstract] [Full Text] [Related]

  • 10. Role of factor V Leiden and prothrombin 20210A in patients with retinal artery occlusion.
    Weger M, Renner W, Pinter O, Stanger O, Temmel W, Fellner P, Schmut O, Haas A.
    Eye (Lond); 2003 Aug 15; 17(6):731-4. PubMed ID: 12928685
    [Abstract] [Full Text] [Related]

  • 11. No association between the 20210 G/A prothrombin gene mutation and premature coronary artery disease.
    Eikelboom JW, Baker RI, Parsons R, Taylor RR, van Bockxmeer FM.
    Thromb Haemost; 1998 Dec 15; 80(6):878-80. PubMed ID: 9869153
    [Abstract] [Full Text] [Related]

  • 12. The HR2 haplotype of factor V is not associated with the risk of myocardial infarction.
    Doggen CJ, de Visser MC, Vos HL, Bertina RM, Cats VM, Rosendaal FR.
    Thromb Haemost; 2000 Nov 15; 84(5):815-8. PubMed ID: 11127862
    [Abstract] [Full Text] [Related]

  • 13. Plasminogen activator inhibitor type 1 (PAI-1) and platelet glycoprotein IIIa (PGIIIa) polymorphisms in young Asian Indians with acute myocardial infarction.
    Pegoraro RJ, Ranjith N.
    Cardiovasc J S Afr; 2005 Nov 15; 16(5):266-70. PubMed ID: 16307159
    [Abstract] [Full Text] [Related]

  • 14. A common thrombomodulin amino acid dimorphism is associated with myocardial infarction.
    Norlund L, Holm J, Zöller B, Ohlin AK.
    Thromb Haemost; 1997 Feb 15; 77(2):248-51. PubMed ID: 9157575
    [Abstract] [Full Text] [Related]

  • 15. Lack of association between factor V Leiden and prothrombin G20210A polymorphisms in Tunisian subjects with a history of myocardial infarction.
    Berredjeb Ben Slama D, Fekih-Mrissa N, Haggui A, Nsiri B, Baraket N, Haouala H, Gritli N.
    Cardiovasc Pathol; 2013 Feb 15; 22(1):39-41. PubMed ID: 22483732
    [Abstract] [Full Text] [Related]

  • 16. The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolism.
    Oguzulgen IK, Yilmaz E, Demirtas S, Erkekol FO, Ekim N, Demir N, Numanoglu N, Ozel D, Ulu A, Akar N.
    Clin Appl Thromb Hemost; 2009 Feb 15; 15(1):73-7. PubMed ID: 18160588
    [Abstract] [Full Text] [Related]

  • 17. The prothrombin 20210A allele and its association with myocardial infarction.
    Croft SA, Daly ME, Steeds RP, Channer KS, Samani NJ, Hampton KK.
    Thromb Haemost; 1999 Jun 15; 81(6):861-4. PubMed ID: 10404757
    [Abstract] [Full Text] [Related]

  • 18. The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.
    Said JM, Brennecke SP, Moses EK, Walker SP, Monagle PT, Campbell J, Bryant VJ, Borg AJ, Higgins JR.
    Aust N Z J Obstet Gynaecol; 2008 Dec 15; 48(6):536-41. PubMed ID: 19133039
    [Abstract] [Full Text] [Related]

  • 19. Thrombophilic gene polymorphisms in puerperal cerebral veno-sinus thrombosis.
    Dindagur N, Kruthika-Vinod TP, Christopher R.
    J Neurol Sci; 2006 Nov 01; 249(1):25-30. PubMed ID: 16839569
    [Abstract] [Full Text] [Related]

  • 20. 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 01; 80(5):743-8. PubMed ID: 9843165
    [Abstract] [Full Text] [Related]

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