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Consultez les derniers articles autour de la maladie de Willebrand

Dernière mise à jour : Vendredi 04 juillet 2025

Delphi consensus recommendations for neuraxial anesthesia in adults with platelet disorders and coagulation defects: communication from the ISTH SSC Subcommittee on von Willebrand Factor

Neuraxial anesthesia is used for pain management in surgical and nonsurgical settings. Spinal/epidural hematomas likely occur in between 1:10 000 and 1:200 000 procedures. Risk is believed to be greater...
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Journal of Thrombosis and Haemostasis 2025; 23(6): 2039-49
Peterson, Wynn et al.

Current and emerging therapies as potential treatment for people with von Willebrand disease

Von Willebrand disease (VWD) reflects the most common inherited bleeding disorder, arising from defects or deficiencies in the von Willebrand factor (VWF). VWD treatment mostly relies on the replacement...
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Expert Review of Hematology 2024; 17(12): 917-33
Emmanuel J. Favaloro et al.

Acquired von Willebrand syndrome secondary to monoclonal gammopathy: a single-center case series.

Acquired von Willebrand syndrome (AVWS) is a well-known complication of a monoclonal gammopathy with a potentially severe bleeding tendency. Treatment with von Willebrand factor (VWF)/factor VIII (FVIII)...
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Therapeutic advances in hematology 2025 ; 16: 20406207251347235
Van Thillo Quentin et al.

Landscape and Spectrum of VWF Variants in Type 2 Von Willebrand Disease: Insights from a German Patient Cohort.

Von Willebrand disease (VWD) type 2 arises from variants in von Willebrand factor (VWF) that disrupt its essential hemostatic functions. Per ISTH guidelines, it is classified as type 2A, 2B, 2M, and 2N based on the affected VWF roles.Objectives: This population-based study aims to uncover the genotype and laboratory phenotypes in type 2 VWD, providing insights into underlying genetics and genotype-phenotype associations....
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Thrombosis and haemostasis 2025 May
Yadegari Hamideh et al.
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