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Role of factor VIII-binding capacity of endogenous von Willebrand factor in the development of factor VIII inhibitors in patients with severe hemophilia A

机译：内源性血管性假血友病因子的因子VIII结合能力在重度A型血友病患者中因子VIII抑制剂发展中的作用

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期刊名称 Haematologica
作者
Yohann Repessé; Catherine Costa; Roberta Palla; Elika Farrokhi Moshai; Annie Borel-Derlon; Roseline D’Oiron; Chantal Rothschild; Amal El-Beshlawy; Mohsen Elalfy; Vijay Ramanan; Peyman Eshghi; Johannes Oldenburg; Anna Pavlova; Frits R Rosendaal; Flora Peyvandi; Srinivas V. Kaveri; Sébastien Lacroix-Desmazes;
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年(卷),期 2019(104),8
年度 2019
页码 e369–e372
总页数 4
原文格式 PDF
正文语种
中图分类血液学检验;
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专利

1. Combined hemophilia A and type 2 von Willebrand's disease: defect of both factor VIII level and factor VIII binding capacity of von Willebrand factor | Haematologica [J] . A Casonato, E Pontara, F Sartorello, Haematologica . 2001,第10期

机译：合并的血友病A和2型冯·威勒布兰德病：von Willebrand因子的VIII因子水平和VIII因子结合能力均存在缺陷|血液学
2. Factor VIII-von Willebrand factor binding defects in autosomal recessive von Willebrand disease type Normandy and in mild hemophilia A. New insights into factor VIII-von Willebrand factor interactions. [J] . Jacquemin M Acta Haematologica . 2009,第2a3期

机译：常染色体隐性隐性冯·威勒布兰德病类型诺曼底和轻度血友病A中的因子VIII-冯·威勒布兰德因子结合缺陷。因子VIII-von Willebrand因子相互作用的新见解。
3. The pro-polypeptide of von Willebrand factor is required for the formation of a functional factor VIII-binding site on mature von Willebrand factor [J] . A Leyte, B Duim, H B Van Schijndel, The biochemical journal . 1991,第1期

机译：在成熟的von Willebrand因子上形成功能性因子VIII结合位点需要von Willebrand因子的原多肽
4. Inactiwatlon of Animal Factor VIII by human Factor VIII Inhibitors: Inwestigation of Plasma from Patients with Inhibitors in congenital Hemophilia I and from Patients with acquired Hemophilia A [C] . V. Aumann, G. Lutze (Jr.), G. Lutze (Sen.), Hemophilie-Symposion . 2003

机译：人为因子VIII抑制剂的动物因子VIII的乙酰丁酮：先天性血友病药中抑制剂患者的血浆中的预防
5. Satisfaction, Adherence, and Recombinant Factor VIII Choice of Patients with Moderate to Severe Hemophilia A [D] . Strickland, Kimberly. 2020

机译：满意度，依从性和重组因素VIII患者中度至重度血友病的患者
6. Alloantibodies to therapeutic factor VIII in hemophilia A: the role of von Willebrand factor in regulating factor VIII immunogenicity [O] . Johannes Oldenburg, Sébastien Lacroix-Desmazes, David Lillicrap 2015

机译：血友病A中治疗因子VIII的同种抗体：血管性血友病因子在调节因子VIII免疫原性中的作用
7. Role of factor VIII-binding capacity of endogenous von Willebrand factor in the development of factor VIII inhibitors in patients with severe hemophilia A [O] . Yohann Repessé, Catherine Costa, Roberta Palla, 2019

机译：因子VIII结合能力的作用在严重血友病患者A患者因子VIII抑制剂发展中的作用
8. Cooperative Study of Spontaneously-Occurring Factor VIII Inhibitors in Patients with Hemophilia A [R] . Shapiro, S. S. 1981

机译：血友病a患者自发性因子VIII抑制剂的合作研究

Role of factor VIII-binding capacity of endogenous von Willebrand factor in the development of factor VIII inhibitors in patients with severe hemophilia A

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