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Check out the latest articles on von Willebrand disease

Last update : Thursday July 30, 2026

Clinical and Laboratory Characterization of Acquired Von Willebrand Syndrome.

Acquired von Willebrand Syndrome (AVWS) is a rare bleeding disorder characterized by quantitative or qualitative defects of von Willebrand factor (VWF) in patients without a personal or family history...
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American Journal of Hematology (2026).
Ciavarella Alessandro et al.

Exploratory Claims-Based Assessment of Diagnosed and Potentially Undiagnosed von Willebrand Disease in Japan.

Von Willebrand disease (VWD) is the most common inheritedbleeding disorder, but its true burden remains difficult to quan-tify because many affected individuals are never diagnosed orare diagnosed only...
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Haemophilia (2026).
Nagao Azusa et al.

Cost comparison of pdVWF/FVIII prophylaxis and on-demand therapy in type 3 von Willebrand disease in the United States

Von Willebrand factor (VWF) concentrate prophylaxis is recommended for patients with severe von Willebrand disease (VWD) or VWD with frequent bleeding symptoms but remains underutilized, in part due to...
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Blood advances (July 2026)
Sidonio, Robert et al.

An Ex Vivo Pharmacodynamic Study of KN057, a Tissue Factor Pathway Inhibitor Neutralizing Antibody, in Plasma Samples From Patients With Haemophilia or VWD3.

Tissue factor pathway inhibitor (TFPI), a key regulator of tissue factor-initiated coagulation through FXa-dependent inhibition of the tissue factor-FVIIa complex, has emerged as a promising target for restoring thrombin generation. Aim: This ex vivo pharmacodynamic study aimed to evaluate the KN057, a novel humanized TFPI-neutralizing antibody, in plasma samples from participants with haemophilia or type 3 von Willebrand disease (VWD3)....
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Haemophilia (2026).
Ju Mankai et al.

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