Discrepancies between von Willebrand factor multimeric composition and other tests in some von Willebrand's disease variants.

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作者信息

Casonato A, Fabris F, De Marco L, Girolami A

出版信息

Blut. 1987 Jul;55(1):61-2. doi: 10.1007/BF00319645.

DOI:10.1007/BF00319645

PMID:3496930

Abstract

摘要

相似文献

Discrepancies between von Willebrand factor multimeric composition and other tests in some von Willebrand's disease variants.

Blut. 1987 Jul;55(1):61-2. doi: 10.1007/BF00319645.

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von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma: a new subtype.血管性血友病，其特征为瑞斯托霉素敏感性增加且血浆中存在所有血管性血友病因子多聚体：一种新的亚型。

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Heterogeneity in von Willebrand's disease.血管性血友病的异质性。

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Variant forms of von Willebrand's disease: type IIA, type IIB and platelet-type von Willebrand's disease.血管性血友病的变异型：IIA型、IIB型和血小板型血管性血友病。

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Ristocetin in the diagnosis of von willebrand's disease: a comparison of rate and percent of aggregation with levels of the plasma factor(s) necessary for ristocetin aggregation.瑞斯托霉素在血管性血友病诊断中的应用：瑞斯托霉素诱导聚集率和聚集百分比与瑞斯托霉素诱导聚集所需血浆因子水平的比较。

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Sulfatide-binding assay for von Willebrand factor. Detection of von Willebrand's disease without discrimination of vWD subtypes.血管性血友病因子的硫脂结合测定。无需区分血管性血友病（vWD）亚型即可检测血管性血友病。

Thromb Res. 2000 Apr 15;98(2):213-9. doi: 10.1016/s0049-3848(99)00232-7.

Laboratory diagnosis of von Willebrand's disease.血管性血友病的实验室诊断

Clin Lab Med. 1994 Dec;14(4):781-94.

Heightened interaction between platelets and factor VIII/von Willebrand factor in a new subtype of von Willebrand's disease.血管性血友病新亚型中血小板与凝血因子VIII/血管性血友病因子之间的相互作用增强。

N Engl J Med. 1980 May 8;302(19):1047-51. doi: 10.1056/NEJM198005083021902.

von Willebrand's variant (type II Buffalo). Thrombocytopenia after desmopressin but absence of in vitro hypersensitivity to ristocetin.

Am J Clin Pathol. 1990 Apr;93(4):522-5. doi: 10.1093/ajcp/93.4.522.

本文引用的文献

Pseudo-von Willebrand's disease. An intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high-molecular-weight multimers.假性血管性血友病。一种血小板内在缺陷，其表现为未修饰的人凝血因子VIII/血管性血友病因子可引起血小板聚集，且其高分子量多聚体的吸附增强。

N Engl J Med. 1982 Feb 11;306(6):326-33. doi: 10.1056/NEJM198202113060603.

Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets.血管性血友病：通过分析血浆和血小板中因子VIII/血管性血友病因子的多聚体组成来鉴定两种亚型

J Clin Invest. 1980 Jun;65(6):1318-25. doi: 10.1172/JCI109795.

N Engl J Med. 1980 May 8;302(19):1047-51. doi: 10.1056/NEJM198005083021902.

The evaluation of factor VIII antigen by means of a simple slide test.通过简单玻片试验评估因子 VIII 抗原。

Am J Clin Pathol. 1985 Jul;84(1):107-11. doi: 10.1093/ajcp/84.1.107.

A new von Willebrand variant (type I, New York): increased ristocetin-induced platelet aggregation and plasma von Willebrand factor containing the full range of multimers.一种新的血管性血友病变异型（I型，纽约型）：瑞斯托霉素诱导的血小板聚集增加，血浆血管性血友病因子包含完整范围的多聚体。

Blood. 1986 Jul;68(1):149-56.

Abnormalities of von Willebrand factor in myeloproliferative disease: a relationship with bleeding diathesis.

Br J Haematol. 1986 May;63(1):75-83. doi: 10.1111/j.1365-2141.1986.tb07497.x.

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