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Consultez les derniers articles autour de la maladie de Willebrand

Dernière mise à jour : Vendredi 08 mai 2026

Prophylaxis for von Willebrand disease: Is it time for parity with established practice in hemophilia A?

A deficiency and/or dysfunction of von Willebrand factor (VWF) or factor VIII (FVIII) results in the bleeding disorders of von Willebrand disease (VWD) and hemophilia A (HA), respectively. Whereas HA impacts...
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Therapeutic advances in hematology 2026 ; 17: 20406207261431617
Sidonio Robert F et al.

Practical Advances in the Diagnosis of Haemophilia and von Willebrand Disease Including Monitoring of Non-Factor Replacement Therapies.

Traditional haemophilia therapies act to replace the relevant missing clotting factor, are not interchangeable between haemophilia A and B and cannot be used in patients with high titre inhibitors. Novel...
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Haemophilia : the official journal of the World Federation of Hemophilia 2026 Apr
Bowyer Annette et al.

Updated Diagnosis of von Willebrand Disease: Global Access, Genomic Insights and Quality Assurance.

One hundred years after its first description, major advances in laboratory science and genetics have transformed the diagnosis and clinical characterization of von Willebrand disease (VWD). This review...
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Haemophilia : the official journal of the World Federation of Hemophilia 2026 Apr
Seidizadeh Omid et al.

Von Willebrand disease as a predictor of postoperative hemorrhagic complications in pediatric adenotonsillar surgery: a retrospective cohort study.


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European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2026 Mar
Gorzelnik Anna et al.

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