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

A Casonato; E Pontara; F Sartorello; D Gemmati; MG Cattini; A Girolami

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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

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

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《Haematologica》 |2001年第10期|共2页
作者
A Casonato; E Pontara; F Sartorello; D Gemmati; MG Cattini; A Girolami;
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中图分类血液及淋巴系疾病;
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1. 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。
2. Hemophilia A, von Willebrand disease, and atherosclerosis of abdominal aorta and leg arteries: factor VIII and von Willebrand factor defects appear to protect abdominal aorta and leg arteries from atherosclerosis. [J] . Bilora F, Boccioletti V, Zanon E, Clinical and applied thrombosis/hemostasis . 2001,第4期

机译：甲型血友病，von Willebrand病和腹主动脉和下肢动脉粥样硬化：VIII因子和von Willebrand因子缺陷似乎可以保护腹主动脉和下肢动脉免受动脉硬化。
3. Von Willebrand Factor (VWF) Propeptide and Factor VIII (FVIII) Levels Identify the Contribution of Decreased Synthesis and/or Increased Clearance Mechanisms in the Pathogenesis of Type 1 Von Willebrand Disease (VWD) in the Zimmerman Program [J] . Haberichter Sandra L., Christopherson Pamela A., Flood Veronica H., Blood: The Journal of the American Society of Hematology . 2016,第22期

机译：冯·威勒布兰德（VWF）肽和因子VIII（FVIII）水平在Zimmerman计划中确定了1型冯·威勒布兰德病（VWD）发病机理中合成减少和/或清除机制增加的贡献
4. IMMUNATE S/D - A new Factor VIII - von-Willebrand Factor Complex Concentrate [C] . P.L. Turecek, W. Schonhofer, T.R. Kreil, Hemophilie-Symposion . 2004

机译：免疫S / D - 一种新因子VIII - von-Willebrand系数复合浓缩物
5. The effect of biomechanical and biochemical regulators on the expression of Factor VIII and von Willebrand Factor in endothelial cells [D] . Leonard, Jacqueline Marianna Morello. 2016

机译：生物力学和生化调节剂对内皮细胞中VIII因子和von Willebrand因子表达的影响
6. 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：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
7. Hemophilia A, von Willebrand Disease, and Atherosclerosis of Abdominal Aorta and Leg Arteries: Factor VIII and von Willebrand Factor Defects Appear to Protect Abdominal Aorta and Leg Arteries From Atherosclerosis [O] . F. Bilora, V. Boccioletti, E. Zanon, 2001

机译：血友病A，von Willebrand疾病和腹主动脉和腿部动脉的动脉粥样硬化：因素VIII和von Willebrand因子缺陷似乎保护动脉粥样硬化的腹部主动脉和腿部动脉
8. Influence of Factor VIII/von Willebrand Factor Protein (F VIII/vWF) and F VIII/vWF-Poor Cryoprecipitate on Post-Ischemic Microvascular Reperfusion in the Central Nervous System [R] . Hallenbeck, J. M., Furlow, T. W., Gralnick, H. R. 1980

机译：因子VIII / von Willebrand因子蛋白（F VIII / vWF）和F VIII / vWF-差冷沉淀物对中枢神经系统缺血后微血管再灌注的影响

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

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