Buchvarova V, Samama M, Lecrubier C
Vutr Boles. 1976;15(3):92-4.
Certain new data about the nature of Willebrand factors are discussed, its activity being considered as part of the activity of the antihemolytic factor VIII. An one-stage method for its determination is described based on the absence of thrombocytic aggregation in the presence of ristocetin in the patients with Willebrand disease as well as the illustration of one case.
讨论了关于血管性血友病因子性质的某些新数据,其活性被视为抗溶血因子VIII活性的一部分。描述了一种基于血管性血友病患者在存在瑞斯托霉素时血小板聚集缺失的一步法测定方法,并举例说明了一个病例。