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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.

Health-related quality of life in children with von Willebrand disease: Results of the French real-life WiSH-QoL study

Haemorrhagic episodes may have physical or psychological effects on children with von Willebrand disease (VWD) and their families. These effects can be measured by health-related quality of life (HRQoL). The WiSH-QoL study aimed at filing this knowledge gap, using generic or disease-specific patient-reported outcome questionnaires (PROs) in France. Patients/Methods This prospective observational...
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Journal of Thrombosis and Haemostasis 2025; AOP:10.1016/j.jtha.2025.05.017
Goudemand, Jenny et al.
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