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Journal Abstract Search

261 related items for PubMed ID: 15377463

  • 1. Molecular basis of von Willebrand disease and its clinical implications.
    Haematologica; 2004 Sep; 89(9):1036. PubMed ID: 15377463
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  • 2. [Willebrand disease].
    Lequièvre V.
    Rev Infirm; 2006 Sep; (122):22-4. PubMed ID: 16881452
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  • 5. Recombinant von Willebrand factor.
    Schwarz HP, Turecek PL, Pichler L, Mitterer A, Mundt W, Dorner F, Roussi J, Drouet L.
    Thromb Haemost; 1997 Jul; 78(1):571-6. PubMed ID: 9198218
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  • 9. [Inborn and acquired von Willebrand disease].
    Schneppenheim R, Budde U.
    Hamostaseologie; 2008 Dec; 28(5):312-9. PubMed ID: 19132162
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  • 11. Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families.
    Castaman G, Giacomelli S, Rodeghiero F.
    Acta Haematol; 2009 Dec; 121(2-3):106-10. PubMed ID: 19506356
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  • 12. Treatment of von Willebrand's disease.
    Logan LJ.
    Hematol Oncol Clin North Am; 1992 Oct; 6(5):1079-94. PubMed ID: 1400073
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  • 13. Prophylaxis in von Willebrand disease.
    Franchini M, Targher G, Lippi G.
    Ann Hematol; 2007 Oct; 86(10):699-704. PubMed ID: 17634944
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  • 19. Type 1 von Willebrand disease: application of emerging data to clinical practice.
    Collins PW, Cumming AM, Goodeve AC, Lillicrap D.
    Haemophilia; 2008 Jul; 14(4):685-96. PubMed ID: 18510569
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