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Consulte los últimos artículos sobre la enfermedad de von Willebrand

Última actualización: Jueves, 18 de julio de 2024

Oral surgery in people with inherited bleeding disorder: A retrospective study

Oral surgery procedures can lead to a moderate or high risk of postoperative bleeding, especially in patients treated with antithrombotic medications or those suffering from inherited bleeding disorders....
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Haemophilia 2024; 30(4): 943-9
Emma Fribourg et al.

The impact of von Willebrand factor on fibrin formation and structure unveiled with type 3 von Willebrand disease plasma

von Willebrand factor (VWF) is a plasma glycoprotein that mediates platelet adhesion at sites of vascular injury and contributes to the process of hemostasis [1,2]. The interaction between VWF and platelets...
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Blood Coagulation & Fibrinolysis 2024; 35(5): 256-64
Martinez-Vargas, Marina et al.

Genetic determinants of enhanced von Willebrand factor clearance from plasma

Enhanced von Willebrand factor (VWF) clearance from plasma is associated with von Willebrand disease (VWD). However, the genetic of this disease mechanism is not well defined. To determine VWF variants...
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Journal of Thrombosis and Haemostasis 2023; 21(5): 1112-22
Seidizadeh, Omid et al.

Von Willebrand Factor (VWF) multiplex activity assay differentiation of type 1 von Willebrand Disease (VWD) and variant VWD

Von Willebrand disease (VWD) is the most common inherited bleeding disorder and is characterized by increased or prolonged mucocutaneous bleeding. Though VWD impacts 0.01% to 0.1% of the population, it remains challenging to reach a definitive diagnosis. VWD classification encompasses three main types: type 1 VWD, type 2 VWD and type 3 VWD. Type 1 VWD is partial quantitative deficiency of von Willebrand factor (VWF), whereas type 3 VWD is essentially...
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Haemophilia 2024; 30(1): 161-8
Jonathan C. Roberts et al.

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