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PUBMED FOR HANDHELDS

Journal Abstract Search


162 related items for PubMed ID: 2148653

  • 1. Hereditary protein S deficiency in young adults with arterial occlusive disease.
    Allaart CF, Aronson DC, Ruys T, Rosendaal FR, van Bockel JH, Bertina RM, Briët E.
    Thromb Haemost; 1990 Oct 22; 64(2):206-10. PubMed ID: 2148653
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  • 3. A Dutch family with hereditary protein S deficiency.
    Petersen EJ, Allaart RC, Meuwissen OJ.
    Neth J Med; 1989 Jun 22; 34(5-6):243-50. PubMed ID: 2528077
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  • 6. Difference in absolute risk of venous and arterial thrombosis between familial protein S deficiency type I and type III. Results from a family cohort study to assess the clinical impact of a laboratory test-based classification.
    Brouwer JL, Veeger NJ, van der Schaaf W, Kluin-Nelemans HC, van der Meer J.
    Br J Haematol; 2005 Mar 22; 128(5):703-10. PubMed ID: 15725093
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  • 8. Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients.
    Eid SS.
    Clin Lab Sci; 2002 Mar 22; 15(4):196-9. PubMed ID: 12776777
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  • 10. [Familial deficiency of protein S associated with thrombophilia].
    Velasco F, Rojas R, Torres A.
    Med Clin (Barc); 1989 Apr 08; 92(13):484-7. PubMed ID: 2526275
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  • 11. Arterial thrombosis and the role of thrombophilia.
    Boekholdt SM, Kramer MH.
    Semin Thromb Hemost; 2007 Sep 08; 33(6):588-96. PubMed ID: 17768691
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  • 16. Contribution of the cystathionine beta-synthase gene (844ins68) polymorphism to the risk of early-onset venous and arterial occlusive disease and of fasting hyperhomocysteinemia.
    de Franchis R, Fermo I, Mazzola G, Sebastio G, Di Minno G, Coppola A, Andria G, D'Angelo A.
    Thromb Haemost; 2000 Oct 08; 84(4):576-82. PubMed ID: 11057853
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  • 19. Severe arterial cerebral thrombosis in a patient with protein S deficiency (moderately reduced total and markedly reduced free protein S): a family study.
    Girolami A, Simioni P, Lazzaro AR, Cordiano I.
    Thromb Haemost; 1989 Feb 28; 61(1):144-7. PubMed ID: 2526383
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  • 20. Hereditary deficiency of antithrombin III, protein C and protein S: prevalence in patients with a history of venous thrombosis and criteria for rational patient screening.
    Pabinger I, Brücker S, Kyrle PA, Schneider B, Korninger HC, Niessner H, Lechner K.
    Blood Coagul Fibrinolysis; 1992 Oct 28; 3(5):547-53. PubMed ID: 1450321
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