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Consulte los últimos artículos sobre la enfermedad de von Willebrand

Última actualización: Jueves, 06 de junio de 2024

Early diagnosis of persons with von Willebrand disease using a machine learning algorithm and real-world data

Von Willebrand disease (VWD) is underdiagnosed, often delaying treatment. VWD claims coding is limited and includes no severity qualifiers; improved identification methods for VWD are needed. The aim of...
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Expert Review of Hematology 2024; 17(6): 261-268
Robert F. Sidonio Jr et al.

Congenital Haemostasis Disorders and Urology Surgery: Is It Safe?

There are no specific recommendations for the management of patients with bleeding disorders (BD), such as haemophilia A (HA), haemophilia B (HB), or von Willebrand disease (WD), in urology surgery. Methods:...
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Journal of clinical medicine 2024 Apr; 13(8)
Bres Antoine et al.

Variant mapping using mass spectrometry-based proteotyping as a diagnostic tool in Von Willebrand Disease

Von Willebrand disease (VWD) is the most common inherited bleeding disorder, characterized by either partial or complete von Willebrand factor (VWF) deficiency or by the occurrence of VWF proteoforms of...
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Journal of Thrombosis and Haemostasis 2024; AOP:10.1016/j.jtha.2024.04.011
Kreft, Iris C. et al.

Type 2M/2A von Willebrand disease: A shared phenotype between type 2M and 2A.

Four variants have been continuously subjected to debate and received different von Willebrand disease (VWD) classifications: p.R1315L, p.R1315C, p.R1374H, and p.R1374C. We chose to comprehensively investigate these variants with full set of VWD tests, protein modeling predictions and structural biology. Patients with p.R1315L, p.R1315C, p.R1374H and p.R1374C were included. Agroup with type 2A and 2M was included to better understand similarities...
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Blood advances 2024 Feb
Seidizadeh Omid et al.

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