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PUBMED FOR HANDHELDS

Journal Abstract Search


185 related items for PubMed ID: 19127092

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  • 3. Upper extremity deep vein thrombosis after suspension of progesterone-only oral treatment.
    Lapecorella M, Orecchioni A, Dell'Orso L, Mariani G.
    Blood Coagul Fibrinolysis; 2007 Jul; 18(5):513-7. PubMed ID: 17581329
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  • 9. Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.
    Altinisik J, Ates O, Ulutin T, Cengiz M, Buyru N.
    Clin Appl Thromb Hemost; 2008 Oct; 14(4):415-20. PubMed ID: 18160601
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  • 11. Ocular vascular thrombotic events: a diagnostic window to familial thrombophilia (compound factor V Leiden and prothrombin gene heterozygosity) and thrombosis.
    Glueck CJ, Wang P.
    Clin Appl Thromb Hemost; 2009 Feb; 15(1):12-8. PubMed ID: 18796459
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  • 15. Pregnancy-associated deep vein thrombosis in a double homozygous carrier of factor V Leiden and prothrombin G20210A.
    Beretta AL, Bianchi M, Norchi S, Martinelli I.
    Thromb Haemost; 2005 Dec; 94(6):1329-30. PubMed ID: 16411414
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  • 16. Recurrent thrombembolic risk in patients with multiple thrombophilic disorders.
    Agoşton-Coldea L, Rusu LD, Bobar C, Rusu ML, Mocan T, Procopciuc LM.
    Rom J Intern Med; 2008 Dec; 46(3):261-6. PubMed ID: 19366087
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  • 17. Prothrombin G20210A Gene Mutation-Induced Recurrent Deep Vein Thrombosis and Pulmonary Embolism: Case Report and Literature Review.
    Elkattawy S, Alyacoub R, Singh KS, Fichadiya H, Kessler W.
    J Investig Med High Impact Case Rep; 2022 Dec; 10():23247096211058486. PubMed ID: 35426321
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  • 20. Severe systemic thrombosis in a young COVID-19 patient with a rare homozygous prothrombin G20210A mutation.
    Fiore JR, Ciarallo M, Di Stefano M, Sica S, Scarale M, D'Errico M, Corallo F, Lo Caputo S, Margaglione M, Santantonio T.
    Infez Med; 2021 Jun 01; 29(2):259-262. PubMed ID: 34061792
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