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...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
Main Authors: Van Genderen, P. J., Papatsonis, D. N., Michiels, J. J., Wielenga, J. J., Stibbe, J., Huikeshoven, F. J.
Format: Artigo
Jezik:Inglês
Izdano: BMJ Group 1994
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC2398043/
https://ncbi.nlm.nih.gov/pubmed/7532860
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki