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Presence of factor VIII-related antigen in blood platelets of patients with Von Willebrand's disease

VON WILLEBRAND'S disease (VWD) is an autosomally inherited disorder characterised by low factor VIII activity (antihaemophilic factor, AHF), prolonged bleeding time, reduced retention of platelets in a glass bead column and abnormal distocetin-induced platelet aggregation. The prolonged bleedin...

詳細記述

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書誌詳細
出版年:Nature
主要な著者: BOUMA, B. N., HORDIJK-HOS, J. M., DE GRAAF, S., SIXMA, J. J., VAN MOURIK, J. A.
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group UK 1975
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC7086501/
https://ncbi.nlm.nih.gov/pubmed/1080838
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/257510a0
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