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Journal Abstract Search

311 related items for PubMed ID: 8584987

  • 21. Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.
    Ireland H, Thompson E, Lane DA.
    Thromb Haemost; 1996 Dec; 76(6):867-73. PubMed ID: 8972002
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  • 22. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S, Keskin N, Keskin A, Atalay E.
    Clin Appl Thromb Hemost; 2007 Apr; 13(2):166-71. PubMed ID: 17456626
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  • 23. Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients.
    Eid SS.
    Clin Lab Sci; 2002 Apr; 15(4):196-9. PubMed ID: 12776777
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  • 24. 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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  • 25. [Activated C protein resistance: laboratory study and prevalence of the defect in the Chilean population].
    Pereira J, Quiroga T, Goycoolea M, Muñoz B, Hidalgo P, Kaltwasser G, Mezzano D.
    Rev Med Chil; 1996 Jun; 124(6):663-8. PubMed ID: 9041721
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  • 29. Prevalence of factor V leiden mutation in patients with thrombosis in Tunisia.
    Ajem A, Slama A, Slama FB, Mehjoub T.
    East Mediterr Health J; 2009 Jun; 15(6):1483-8. PubMed ID: 20218141
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  • 30. Inherited resistance to activated protein C, a major basis of venous thrombosis, is caused by deficient anticoagulant cofactor function of factor V.
    Dahlbäck B.
    Haematologica; 1995 Jun; 80(2 Suppl):102-13. PubMed ID: 7628762
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  • 32. [Activated protein C resistance as a cause of thrombophilia].
    Ruiz-Argüelles GJ.
    Rev Invest Clin; 1996 Jun; 48(3):223-9. PubMed ID: 8966383
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  • 38. Activated protein C resistance in anterior ischaemic optic neuropathy.
    Nagy V, Facsko A, Takacs L, Balazs E, Berta A, Balogh I, Edes I, Czuriga I, Pfliegler G.
    Acta Ophthalmol Scand; 2004 Apr; 82(2):140-3. PubMed ID: 15043529
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  • 39. Coexistence of hereditary homocystinuria and factor V Leiden--effect on thrombosis.
    Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U.
    N Engl J Med; 1996 Mar 21; 334(12):763-8. PubMed ID: 8592550
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  • 40. Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V leiden.
    Beauchamp NJ, Daly ME, Cooper PC, Makris M, Preston FE, Peake IR.
    Blood; 1996 Sep 01; 88(5):1700-7. PubMed ID: 8781426
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