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瑞斯托霉素-血管性血友病因子检测及瑞斯托霉素诱导的血小板聚集评估。

Evaluation of ristocetin-Willebrand factor assay and ristocetin-induced platelet aggregation.

作者信息

Olson J D, Brockway W J, Fass D N, Magnuson M A, Bowie E J

出版信息

Am J Clin Pathol. 1975 Feb;63(2):210-8. doi: 10.1093/ajcp/63.2.210.

DOI:10.1093/ajcp/63.2.210
PMID:1078748
Abstract

Normal subjects, patients with various bleeding disorders, and patients with von Willebrand's disease were studied. All patients with von Willebrand's disease had decreased levels of ristocetin-Willebrand factor (range, 0 to 41%) as compared with all other subjects (range, 79 to 202%). Ristocetin-induced platelet aggregation of platelet-rich plasma was abnormal in all patients with von Willebrand's disease tested, and it was possible to correct this abnormal response by addition of normal platelet-poor plasma. Abnormal ristocetin-induced platelet aggregation was seen in patients with intrinsic platelet disorders or, on some occasions, in normal patients who had ingested aspirin. Ristocetin-induced platelet aggregation is not diagnostic, but it may be useful as a simple screening test for patients with possible von Willebrand's disease. In conjunction with other tests, the assay for ristocetin-Willebrand factor will be useful in diagnosis and evaluation of these patients.

摘要

对正常受试者、患有各种出血性疾病的患者以及患有血管性血友病的患者进行了研究。与所有其他受试者(范围为79%至202%)相比,所有血管性血友病患者的瑞斯托霉素-血管性血友病因子水平均降低(范围为0至41%)。在所有接受测试的血管性血友病患者中,富含血小板血浆的瑞斯托霉素诱导的血小板聚集均异常,并且通过添加正常的乏血小板血浆有可能纠正这种异常反应。在患有血小板内在疾病的患者中,或者在某些情况下,在摄入阿司匹林的正常患者中,可见瑞斯托霉素诱导的血小板聚集异常。瑞斯托霉素诱导的血小板聚集不具有诊断性,但它可能作为对可能患有血管性血友病的患者的一种简单筛查试验有用。与其他测试相结合,瑞斯托霉素-血管性血友病因子检测将有助于这些患者的诊断和评估。

相似文献

1
Evaluation of ristocetin-Willebrand factor assay and ristocetin-induced platelet aggregation.瑞斯托霉素-血管性血友病因子检测及瑞斯托霉素诱导的血小板聚集评估。
Am J Clin Pathol. 1975 Feb;63(2):210-8. doi: 10.1093/ajcp/63.2.210.
2
Dissociation between factor VIII (activity and antigen) and ristocetin-induced platelet aggregation in von Willebrand's disease.血管性血友病中因子VIII(活性与抗原)及瑞斯托霉素诱导的血小板聚集之间的解离
Acta Haematol. 1975;53(1):44-8. doi: 10.1159/000208154.
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Diagnosis of von Willebrand's disease. A comparative study of diagnostic tests on nine families with von Willebrand's disease and its differential diagnosis from hemophilia and thrombocytopathy.血管性血友病的诊断。对九个血管性血友病家族的诊断试验及其与血友病和血小板病的鉴别诊断的比较研究。
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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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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.
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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.
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Abnormalities of factor VIII and platelet aggregation--use of ristocetin in diagnosing the von Willebrand syndrome.因子VIII异常与血小板聚集——瑞斯托菌素在血管性血友病诊断中的应用。
Blood. 1975 Mar;45(3):403-12.
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[The laboratory diagnosis of von Willebrand's disease (author's transl)].血管性血友病的实验室诊断(作者译)
Wien Klin Wochenschr. 1976 Apr 2;88(7):221-31.
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Relationship between ristocetin-induced platelet aggregation and factor VIII (activity and antigen) in v. Willebrand's disease.血管性血友病中瑞斯托霉素诱导的血小板聚集与因子VIII(活性和抗原)之间的关系。
Blut. 1974 Oct;29(4):260-4. doi: 10.1007/BF01635547.
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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.

引用本文的文献

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A Comparative Evaluation of an Automated Functional Assay for Von Willebrand Factor Activity in Type 1 Von Willebrand Disease.1型血管性血友病中血管性血友病因子活性自动功能检测的比较评估
Int J Gen Med. 2021 Sep 2;14:5167-5174. doi: 10.2147/IJGM.S321605. eCollection 2021.
2
von Willebrand factor antigen compared with other factors in vasculitic syndromes.血管炎综合征中血管性血友病因子抗原与其他因子的比较。
Arch Dis Child. 1994 Jan;70(1):40-3. doi: 10.1136/adc.70.1.40.
3
von Willebrand protein facilitates platelet incorporation in polymerizing fibrin.
血管性血友病因子促进血小板掺入正在聚合的纤维蛋白中。
J Clin Invest. 1986 Oct;78(4):1112-9. doi: 10.1172/JCI112668.
4
Transplantation of normal bone marrow into a pig with severe von Willebrand's disease.将正常骨髓移植到患有严重血管性血友病的猪体内。
J Clin Invest. 1986 Jul;78(1):26-30. doi: 10.1172/JCI112560.
5
Structural basis of von Willebrand factor binding to platelet glycoprotein Ib and collagen. Effects of disulfide reduction and limited proteolysis of polymeric von Willebrand factor.血管性血友病因子与血小板糖蛋白 Ib 及胶原蛋白结合的结构基础。聚合物血管性血友病因子的二硫键还原及有限蛋白酶解的影响。
J Clin Invest. 1986 Mar;77(3):743-9. doi: 10.1172/JCI112369.
6
Binding and covalent cross-linking of purified von Willebrand factor to native monomeric collagen.纯化的血管性血友病因子与天然单体胶原蛋白的结合及共价交联。
J Clin Invest. 1986 Aug;78(2):551-6. doi: 10.1172/JCI112608.
7
A monoclonal antibody to von Willebrand factor (vWF) inhibits factor VIII binding. Localization of its antigenic determinant to a nonadecapeptide at the amino terminus of the mature vWF polypeptide.一种针对血管性血友病因子(vWF)的单克隆抗体可抑制因子VIII的结合。其抗原决定簇定位于成熟vWF多肽氨基末端的一个十九肽上。
J Clin Invest. 1989 Jul;84(1):56-61. doi: 10.1172/JCI114169.
8
Resistance to arteriosclerosis in pigs with von Willebrand's disease. Spontaneous and high cholesterol diet-induced arteriosclerosis.血管性血友病猪对动脉粥样硬化的抵抗作用。自发性及高胆固醇饮食诱导的动脉粥样硬化。
J Clin Invest. 1978 Mar;61(3):722-30. doi: 10.1172/JCI108985.
9
Bleeding in renal failure: is von Willebrand factor implicated?肾衰竭中的出血:血管性血友病因子是否与之有关?
Br Med J. 1977 Aug 6;2(6083):359-61. doi: 10.1136/bmj.2.6083.359.
10
Studies on the altered electrophoretic type of the factor VIII related antigen.
Hum Genet. 1976 Dec 29;35(1):71-7. doi: 10.1007/BF00295620.