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Consulte los últimos artículos sobre la enfermedad de von Willebrand

Última actualización: Viernes, 05 de diciembre de 2025

A novel cause of type 1 von Willebrand disease: impaired exocytosis of Weibel-Palade bodies due to biallelic MADD variants

The regulated secretion of von Willebrand factor (VWF) from Weibel-Palade bodies (WPBs) in endothelial cells is fundamental to hemostasis. This process relies on recruiting Rab GTPases and their effectors...
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Blood 2025; 146(17): 2133-44
Hordijk, Sophie et al.

Von Willebrand factor and von Willebrand disease in ageing: mechanisms, evolving phenotypes, and clinical implications

The global population is ageing and this demographic shift has profound effects on haemostasis, notably a progressive tilt towards a hypercoagulable state. A major age-associated change in haemostasis...
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The Lancet Haematology 2025; 12(11): e908-e917
Seidizadeh, Omid et al.

High Rates of Post-Tonsillectomy Hemorrhage in ChildrenWith von Willebrand Disease

Though tonsillectomies are commonly performed in children, the rate of post-tonsillectomy hemorrhage in those with von Willebrand disease (VWD) is unknown. Objectives: To determine the rate of post-tonsillectomy...
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Pediatric Blood & Cancer (2025).
Clay T. Cohen et al.

Treatment of von Willebrand Disease.

Treatment for von Willebrand disease (VWD), the most common inherited bleeding disorder, has advanced considerably since its initial description by Erik von Willebrand first described a family in the Åland Islands with severe bleeding. Infusion of von Willebrand factor (VWF) containing concentrates continue to serve as the foundation of management in addition to desmopressin, hormonal therapies, and antifibrinolytic agents such as tranexamic...
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Blood advances 2025 Nov
Connell Nathan T.
Willebrandxpert Encuesta

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