High-dose intravenous gammaglobulin therapy for acquired von Willebrand disease.

Patients with acquired von Willebrand disease may present with severe bleeding, which is usually difficult to manage. Adequate haemostasis in acquired von Willebrand disease may be achieved with the infusion of factor VIII/von Willebrand factor concentrates or with the administration of desmopressin...

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Autori principali: Van Genderen, P. J., Papatsonis, D. N., Michiels, J. J., Wielenga, J. J., Stibbe, J., Huikeshoven, F. J.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 1994
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2398043/
https://ncbi.nlm.nih.gov/pubmed/7532860
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