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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.

PMID:310585
Abstract
摘要

相似文献

1
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.
2
Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content.对血管性血友病中缺乏的、血小板聚集所必需的一种血浆因子进行定量测定。与凝血因子VIII促凝活性及抗原含量的关系。
J Clin Invest. 1973 Nov;52(11):2708-16. doi: 10.1172/JCI107465.
3
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。
J Clin Invest. 1973 Nov;52(11):2697-707. doi: 10.1172/JCI107464.
4
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。
J Lab Clin Med. 1981 Mar;97(3):332-44.
5
[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
Rinsho Byori. 1983 Nov;31(11):1176-85.
6
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
Thromb Haemost. 1983 Aug 30;50(2):509-12.
7
Studies of the human factor VIII/von Willebrand factor protein. III. Qualitative defects in von Willebrand's disease.人凝血因子VIII/血管性血友病因子蛋白的研究。III. 血管性血友病的定性缺陷。
J Clin Invest. 1975 Oct;56(4):814-27. doi: 10.1172/JCI108160.
8
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
J Lab Clin Med. 1983 Mar;101(3):411-25.
9
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
Wien Klin Wochenschr. 1982 Oct 15;94(19):509-14.
10
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
J Lab Clin Med. 1976 Jun;87(6):976-86.

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1
Factor VIII related antigen in the assessment of vasculitis.血管炎评估中的VIII因子相关抗原
Ann Rheum Dis. 1987 Jun;46(6):441-7. doi: 10.1136/ard.46.6.441.