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400 related items for PubMed ID: 20008189

  • 1. Optimizing treatment of von Willebrand disease by using phenotypic and molecular data.
    Rodeghiero F, Castaman G, Tosetto A.
    Hematology Am Soc Hematol Educ Program; 2009; ():113-23. PubMed ID: 20008189
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  • 2. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio.
    Gadisseur A, Berneman Z, Schroyens W, Michiels JJ.
    Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359
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  • 3. Dominant von Willebrand disease type 2A groups I and II due to missense mutations in the A2 domain of the von Willebrand factor gene: diagnosis and management.
    Michiels JJ, van Vliet HH.
    Acta Haematol; 2009; 121(2-3):154-66. PubMed ID: 19506362
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  • 7. Diagnosis and management of von Willebrand disease in Australia.
    Favaloro EJ, Bonar R, Favaloro J, Koutts J.
    Semin Thromb Hemost; 2011 Jul; 37(5):542-54. PubMed ID: 22102198
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  • 8. Intravenous DDAVP and factor VIII-von Willebrand factor concentrate for the treatment and prophylaxis of bleedings in patients With von Willebrand disease type 1, 2 and 3.
    Michiels JJ, van Vliet HH, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van der Velden A, Budde U.
    Clin Appl Thromb Hemost; 2007 Jan; 13(1):14-34. PubMed ID: 17164493
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  • 18. How I treat patients with von Willebrand disease.
    Mannucci PM.
    Blood; 2001 Apr 01; 97(7):1915-9. PubMed ID: 11264151
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