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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...

詳細記述

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書誌詳細
主要な著者: Van Genderen, P. J., Papatsonis, D. N., Michiels, J. J., Wielenga, J. J., Stibbe, J., Huikeshoven, F. J.
フォーマット: Artigo
言語:Inglês
出版事項: BMJ Group 1994
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2398043/
https://ncbi.nlm.nih.gov/pubmed/7532860
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