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PUBMED FOR HANDHELDS

Journal Abstract Search


235 related items for PubMed ID: 9833534

  • 1. [Variant type von Willebrand disease with defective binding to factor VIII].
    Shima M.
    Ryoikibetsu Shokogun Shirizu; 1998; (21 Pt 2):430-3. PubMed ID: 9833534
    [No Abstract] [Full Text] [Related]

  • 2. Update on the management of von Willebrand disease.
    Federici AB.
    Clin Adv Hematol Oncol; 2008 Jan; 6(1):29-30. PubMed ID: 18322438
    [No Abstract] [Full Text] [Related]

  • 3. [Acquired von Willebranol syndrome--its pathophysiology, diagnosis and treatment].
    Mohri H.
    Rinsho Ketsueki; 2001 Jul; 42(7):525-36. PubMed ID: 11524842
    [No Abstract] [Full Text] [Related]

  • 4. Prophylaxis in von Willebrand disease.
    Franchini M, Targher G, Lippi G.
    Ann Hematol; 2007 Oct; 86(10):699-704. PubMed ID: 17634944
    [Abstract] [Full Text] [Related]

  • 5. [Willebrand disease].
    Lequièvre V.
    Rev Infirm; 2006 Oct; (122):22-4. PubMed ID: 16881452
    [No Abstract] [Full Text] [Related]

  • 6. Identification of a His54Gln substitution in von Willebrand factor from a patient with defective binding of factor VIII.
    Rick ME, Krizek DM.
    Am J Hematol; 1996 Apr; 51(4):302-6. PubMed ID: 8602631
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  • 9. Post-DDAVP thrombocytopenia in type 2B von Willebrand disease is not associated with platelet consumption: failure to demonstrate glycocalicin increase or platelet activation.
    Casonato A, Steffan A, Pontara E, Zucchetto A, Rossi C, De Marco L, Girolami A.
    Thromb Haemost; 1999 Feb; 81(2):224-8. PubMed ID: 10063996
    [Abstract] [Full Text] [Related]

  • 10. Von Willebrand factor/factor VIII concentrates in the treatment of von Willebrand disease.
    Batlle J, López-Fernández MF, Fraga EL, Trillo AR, Pérez-Rodríguez MA.
    Blood Coagul Fibrinolysis; 2009 Mar; 20(2):89-100. PubMed ID: 19786936
    [Abstract] [Full Text] [Related]

  • 11. 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
    [No Abstract] [Full Text] [Related]

  • 12. Diagnosis and management of von Willebrand disease in Iran.
    Cohan N, Karimi M.
    Semin Thromb Hemost; 2011 Jul; 37(5):602-6. PubMed ID: 22102206
    [Abstract] [Full Text] [Related]

  • 13. Assessment of primary haemostasis with a new recombinant von Willebrand factor in patients with von Willebrand disease.
    Trossaërt M, Flaujac C, Jeanpierre E, Drillaud N, Sigaud M, Fouassier M, Ternisien C, de Raucourt E.
    Haemophilia; 2020 Mar; 26(2):e44-e48. PubMed ID: 31865618
    [No Abstract] [Full Text] [Related]

  • 14. [Importance of the study of the binding of factor VIII to von Willebrand factor in hemophilia A].
    Batlle J, Blanco-López MJ, Castiñeira MP, López-Fernández MF.
    Sangre (Barc); 1992 Jun; 37(3):211-24. PubMed ID: 1359656
    [No Abstract] [Full Text] [Related]

  • 15. Managing patients with von Willebrand disease type 1, 2 and 3 with desmopressin and von Willebrand factor-factor VIII concentrate in surgical settings.
    Michiels JJ, van Vliet HH, Berneman Z, Schroyens W, Gadisseur A.
    Acta Haematol; 2009 Jun; 121(2-3):167-76. PubMed ID: 19506363
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  • 17. 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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