正常、血友病及血管性血友病患者血小板组分中与凝血因子VIII相关的活性 - Suppr | 超能文献

Factor VIII-related activities in normal, haemophilic and von Willebrand's disease platelet fractions.

作者信息

Meucci P, Peake I R, Bloom A L

出版信息

Thromb Haemost. 1978 Oct 31;40(2):288-301.

Abstract

摘要

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Factor VIII-related activities in normal, haemophilic and von Willebrand's disease platelet fractions.正常、血友病及血管性血友病患者血小板组分中与凝血因子VIII相关的活性

Thromb Haemost. 1978 Oct 31;40(2):288-301.

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J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.

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Defective ristocetin-induced platelet aggregation in von Willebrand's disease and its correction by factor VIII.血管性血友病中瑞斯托霉素诱导的血小板聚集缺陷及其通过因子VIII的纠正。

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Survival of iodine-125-labeled factor VIII in patients with von Willebrand's disease.125碘标记的因子VIII在血管性血友病患者中的存活情况。

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[Pathophysiology of platelet anomalies and its analysis. (4). Abnormality of the platelet function in von Willebrand's disease].血小板异常的病理生理学及其分析。（4）血管性血友病中血小板功能异常

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Gel filtration patterns of factor VIII coagulant antigen and factor VIII related antigen in normal and von Willebrand's disease.正常人和血管性血友病患者中凝血因子VIII促凝抗原及因子VIII相关抗原的凝胶过滤模式

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Heterogeneous abnormalities in the multimeric structure, antigenic properties, and plasma-platelet content of factor VIII/von Willebrand factor in subtypes of classic (type I) and variant (type IIA) von Willebrand's disease.经典（I型）和变异型（IIA型）血管性血友病亚型中VIII因子/血管性血友病因子的多聚体结构、抗原特性及血浆-血小板含量的异质性异常

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Development and present status of concentrate therapy for hemophilia and von Willebrand's disease.血友病和血管性血友病浓缩物治疗的发展与现状

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Platelet-bound ristocetin aggregation factor in normal subjects and patients with von Willebrand's disease.正常受试者及血管性血友病患者血小板结合的瑞斯托菌素聚集因子

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