The Association of Elevated Factor VIII and von Willebrand Factor (vWF) Levels with SYNTAX Score in Patients with Chronic Coronary Syndrome [0.03%]
慢性冠脉综合征患者FXIII和vWF水平升高与SYNTAX评分的关系研究
Predrag Djuric,Zorica Mladenovic,Zoran Jovic et al.
Predrag Djuric et al.
Background and Objectives: Factor VIII (FVIII) and the von Willebrand factor (vWF) are key components of hemostatic balance. Disruption of the vWF-ADAMTS13 axis, characterized by elevated vWF and reduced ADAMTS13 activity has been implicate...
Managing Anesthesia for a Patient With Von Willebrand Disease: A Case Report [0.03%]
1例血管性血友病患者麻醉管理的病例报告
Joshua Singavarapu,Galina Borodulina
Joshua Singavarapu
Von Willebrand disease (vWD) is a common inherited bleeding disorder caused by a deficiency of von Willebrand factor (vWF), a glycoprotein involved in hemostasis. The two major roles of vWF are platelet adhesion and the stabilization of fac...
Case Reports
Cureus. 2025 Aug 24;17(8):e90876. DOI:10.7759/cureus.90876 2025
Managing High Risk Pregnancy in Single Ventricle Physiology with Acquired von Willebrand Disease: A Case Report [0.03%]
单心室解剖合并获得性13型血管性血友病妊娠期管理一例报告
Yash Nagpal,Nisha Chachad,Paola Andrea Benito et al.
Yash Nagpal et al.
Background and Clinical Significance: Left ventricular hypoplasia is often repaired surgically in sequence to a Fontan circulation, which is a physiologic state that presents unique challenges during pregnancy. Although women with Fontan ph...
Case Reports
Reports (MDPI). 2025 Aug 26;8(3):157. DOI:10.3390/reports8030157 2025
Corrigendum to "The Role of von Willebrand Factor in the Pathogenesis of C3 Glomerulopathy" [ Kidney International Reports Volume 10, Issue 6, June 2025, Pages 1929-1938] [0.03%]
关于“von Willebrand因子在C3肾小球病发病机制中的作用”的勘误(肾脏国际报告 第10卷，第6期，2025年6月，第1929-1938页)
Zixin Hua,Yunying Chen,Shasha Han et al.
Zixin Hua et al.
[This corrects the article DOI: 10.1016/j.ekir.2025.03.058.]. © 2025 International Society of Nephrology. Published by Elsevier Inc.
Published Erratum
Kidney international reports. 2025 Jun 25;10(9):3295. DOI:10.1016/j.ekir.2025.06.045 2025
Functional characterization of complement receptor 3 (CR3) in Nile tilapia (Oreochromis niloticus): Insights into CD11b/CD18-mediated immunity against bacterial infections [0.03%]
尼罗罗非鱼补体受体3(CR3)的功能表征：CD11b/CD18介导的细菌感染免疫新见解
Yang Lei,Weiheng Shi,Yanxi Guo et al.
Yang Lei et al.
Keywords: Bacterial infection; Complement receptor 3 (CR3); Immunity; Oreochromis niloticus; von willebrand factor type A (vWFA) domain. Copyright © 2025 Elsevier Ltd. All rights reserved.
Associations of plasma von Willebrand Factor levels with cognitive decline and neurodegeneration in older adults without dementia [0.03%]
老年无痴呆症患者中血浆vWF水平与认知衰退和神经退行性病变的关系
Pan Fu,Meiling Hu
Pan Fu
Background: Previous studies have suggested that von Willebrand Factor (VWF) may be implicated in the pathogenesis of Alzheimer's disease (AD). However, the association between plasma VWF levels and cognitive decline and ...
Correction of von Willebrand factor multimerization in type 2A/ⅡC von Willebrand disease by exogenous VWF propeptide supplementation [0.03%]
Von Willebrand因子前肽外源补充可纠正2A/ⅡC型血管性血友病患者多聚体异常
Ziqi Zhang,Qian Liang,Xiaoqian Xu et al.
Ziqi Zhang et al.
Gene therapy remains the only cure for von Willebrand disease (VWD), but is limited by the large von Willebrand factor (VWF) gene size. Variants affecting the VWF propeptide (VWFpp) impair multimerization, causing type 2A/IIC VWD. VWFpp ser...
Prevalence and Impact of Heavy Menstrual Bleeding in Women With von Willebrand Disease Across Age Groups: A Retrospective Study [0.03%]
不同年龄段血管性血友病女性的月经过多及其影响：一项回顾性研究
Anna Olsson,Petra Elfvinge,Eva Zetterberg et al.
Anna Olsson et al.
Introduction: Heavy menstrual bleeding (HMB) is a common and burdensome symptom in women with von Willebrand disease (VWD). Although VWD and HMB have been studied, the prevalence and impact of HMB across different age gro...
Developing an AI-Generated Peptide Targeting Platelet-type von Willebrand Disease [0.03%]
开发针对Platelet型von Willebrand疾病的AI生成肽类药物的研究
Thomas David Daniel Kazmirchuk,Jiashu Wang,Loredana Bury et al.
Thomas David Daniel Kazmirchuk et al.
Platelet-type von Willebrand disease (PT-VWD) is a rare bleeding disorder caused by gain-of-function mutations in platelet glycoprotein Ib alpha (GPIbα). These mutations lead to a hyperactive protein-protein interaction (PPI) with von Will...
Determining the Impact of Combination Oral Contraceptives on Von Willebrand Factor and Factor VIII in Healthy Patients and Patients With Von Willebrand Disease: A Scoping Review and Meta-Analysis [0.03%]
口服避孕药对血管性血友病患者和非血管性血友病患者的von Willebrand因子和Ⅷ因子的影响：系统综述和荟萃分析
Eve Justason,Anna M Ishchuk,Benjamin P Ott et al.
Eve Justason et al.
Keywords: combined oral contraceptives; estradiol congeners; factor VIII; progestins; von willebrand disease; von willebrand factor. © 2025 The Author(s). Haemophilia published by John Wiley & Sons Ltd.
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