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Journal Abstract Search

1493 related items for PubMed ID: 9599650

  • 1. Molecular genetics of von Willebrand disease.
    Mazurier C, Ribba AS, Gaucher C, Meyer D.
    Ann Genet; 1998; 41(1):34-43. PubMed ID: 9599650
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  • 6. Dominant von Willebrand disease type 2M and 2U are variable expressions of one distinct disease entity caused by loss-of-function mutations in the A1 domain of the von Willebrand factor gene.
    Gadisseur A, van der Planken M, Schroyens W, Berneman Z, Michiels JJ.
    Acta Haematol; 2009; 121(2-3):145-53. PubMed ID: 19506361
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  • 13. Platelet activation and aggregation induced by recombinant von Willebrand factors reproducing four type 2B von Willebrand disease missense mutations.
    de Romeuf C, Hilbert L, Mazurier C.
    Thromb Haemost; 1998 Jan; 79(1):211-6. PubMed ID: 9459349
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  • 18. Type 2M vWD resulting from a lysine deletion within a four lysine residue repeat in the A1 loop of von Willebrand factor.
    Hilbert L, Jenkins PV, Gaucher C, Meriane E, Collins PW, Pasi KJ, Mazurier C.
    Thromb Haemost; 2000 Aug; 84(2):188-94. PubMed ID: 10959688
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  • 20. Diagnosis of inherited von Willebrand disease: a clinical perspective.
    Federici AB.
    Semin Thromb Hemost; 2006 Sep; 32(6):555-65. PubMed ID: 16977566
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