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Journal Abstract Search

135 related items for PubMed ID: 11686335

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  • 22. Homozygotes for prothrombin gene 20210 A allele in a thrombophilic family without clinical manifestations of venous thromboembolism.
    Souto JC, Mateo J, Soria JM, Llobet D, Coll I, Borrell M, Fontcuberta J.
    Haematologica; 1999 Jul; 84(7):627-32. PubMed ID: 10406905
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  • 24. Prevalence of thrombophilia in women with severe ovarian hyperstimulation syndrome and cost-effectiveness of screening.
    Fábregues F, Tàssies D, Reverter JC, Carmona F, Ordinas A, Balasch J.
    Fertil Steril; 2004 Apr; 81(4):989-95. PubMed ID: 15066453
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  • 25. The impact of heterozygosity for the factor V Leiden and factor II G20210A mutations on the risk of thrombosis in Greek patients.
    Hatzaki A, Anagnostopoulou E, Metaxa-Mariatou V, Melissinos C, Philalithis P, Iliadis K, Kontaxis A, Liberatos K, Pangratis N, Nasioulas G.
    Int Angiol; 2003 Mar; 22(1):79-82. PubMed ID: 12771861
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  • 26. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
    Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.
    Laryngoscope; 2007 Mar; 117(3):547-51. PubMed ID: 17334320
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  • 27. Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery.
    Wåhlander K, Larson G, Lindahl TL, Andersson C, Frison L, Gustafsson D, Bylock A, Eriksson BI.
    Thromb Haemost; 2002 Apr; 87(4):580-5. PubMed ID: 12008938
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  • 28. Prothrombin G20210A mutation in Turkish children with thrombosis and the frequency of prothrombin C20209T.
    Gurgey A, Unal S, Okur H, Duru F, Gumruk F.
    Pediatr Hematol Oncol; 2005 Jun; 22(4):309-14. PubMed ID: 16020118
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  • 29. A preliminary study on the role of inherited prothrombotic risk factors in Taiwanese patients with sudden sensorineural hearing loss.
    Lan MY, Shiao JY, Hsu YB, Lin FY, Lin JC.
    Eur Arch Otorhinolaryngol; 2011 Jun; 268(6):817-22. PubMed ID: 21170721
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  • 30. Thrombosis-associated gene variants in sickle cell anemia.
    Romana M, Muralitharan S, Ramasawmy R, Nagel RL, Krishnamoorthy R.
    Thromb Haemost; 2002 Feb; 87(2):356-8. PubMed ID: 11858507
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  • 39. Deep vein thrombosis followed by internal jugular vein thrombosis as a complication of in vitro fertilization in a woman heterozygous for the prothrombin 3' UTR and factor V Leiden mutations.
    McGowan BM, Kay LA, Perry DJ.
    Am J Hematol; 2003 Aug; 73(4):276-8. PubMed ID: 12879433
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  • 40. Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
    Boinot C, Borgel D, Kitzis A, Guicheteau M, Aiach M, Alhenc-Gelas M.
    Blood Coagul Fibrinolysis; 2003 Feb; 14(2):191-6. PubMed ID: 12632031
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