Consulte los últimos artículos sobre la enfermedad de von Willebrand
Última actualización: Jueves, 03 de abril de 2025von Willebrand disease (VWD) is the most common inherited bleeding disorder characterized by defects in the quantity or function of the von Willebrand factor (VWF). The diagnosis of VWD is complex, requiring...
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Heavy menstrual bleeding (HMB) is excessive menstrual blood loss that interferes with an individual’s quality of life. Many individuals with HMB are inadequately managed by health care providers....
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Bleeding in the GI tract continues to pose a therapeutic challenge for clinicians in patients with Von Willebrand Disease (VWD). It is associated with significant morbidity and mortality and represents...
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Clinical trial programs for inherited bleeding disorders feature an array of innovative prophylaxis options: engineered clotting factor concentrates, FVIIIa mimetics, gene therapies, and biologics to bolster thrombin generation (rebalancing agents). Increasingly, non-hemophilia bleeding disorders and a broader demographic (females, children, and infants) are being incorporated into study populations. Ongoing clinical trials broadly address three themes:...
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2 The future of siRNA-mediated approaches to treat von Willebrand disease
Expert Review of Hematology, 17:10, 713-7213 Challenges and considerations of genetic testing in von Willebrand disease
Research and Practice in Thrombosis and Haemostasis 2025; 9(1): 102686Refine su búsqueda de información científica
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