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Journal Abstract Search

136 related items for PubMed ID: 16244770

  • 21. The 4G/4G polymorphism of the hypofibrinolytic plasminogen activator inhibitor type 1 gene: an independent risk factor for serious pregnancy complications.
    Glueck CJ, Phillips H, Cameron D, Wang P, Fontaine RN, Moore SK, Sieve-Smith L, Tracy T.
    Metabolism; 2000 Jul; 49(7):845-52. PubMed ID: 10909993
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  • 27. Role of inherited thrombophilic profile on survival of patients with sepsis.
    Georgakopoulou A, Papadimitriou-Olivgeris M, Karakantza M, Marangos M.
    J Investig Med; 2019 Dec; 67(8):1131-1135. PubMed ID: 31300468
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  • 30. The role of hypercoagulability in ischemic colitis.
    Tsimperidis AG, Kapsoritakis AN, Linardou IA, Psychos AK, Papageorgiou AA, Vamvakopoulos NC, Kyriakou DS, Potamianos SP.
    Scand J Gastroenterol; 2015 Jul; 50(7):848-55. PubMed ID: 25656775
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  • 32. Thrombophilia and unexplained pregnancy loss in Indian patients.
    Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K.
    Natl Med J India; 2008 Jul; 21(3):116-9. PubMed ID: 19004141
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  • 36. Thrombophilia as a cause for central and branch retinal artery occlusion in patients without an apparent embolic source.
    Salomon O, Huna-Baron R, Moisseiev J, Rosenberg N, Rubovitz A, Steinberg DM, Davidson J, Sela BA, Seligsohn U.
    Eye (Lond); 2001 Aug; 15(Pt 4):511-4. PubMed ID: 11767028
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  • 37. Venous thromboembolism in young patients from western India: a study.
    Ghosh K, Shetty S, Madkaikar M, Pawar A, Nair S, Khare A, Pathare A, Jijina F, Mohanty D.
    Clin Appl Thromb Hemost; 2001 Apr; 7(2):158-65. PubMed ID: 11292195
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  • 38. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
    Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.
    Ann Otol Rhinol Laryngol; 2006 Mar; 115(3):195-200. PubMed ID: 16572609
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