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Transition readiness among adolescents and young adults with haemophilia in the Netherlands
Major differences in clinical presentation, diagnosis and management of men and women with autosomal inherited bleeding disorders
BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease
Perioperative treatment of hemophilia A patients: blood group O patients are at risk of bleeding complications
Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study
Prediction of DDAVP response in 850 non-severe hemophilia A patients
Von Willebrand Factor antigen and age explain variation in baseline FVIII:C among nonsevere hemophilia A patients with the same F8 genotype (Arg593Cys and Asn618Ser)
Von Willebrand disease and aging: an evolving phenotype
Reduced prevalence of arterial thrombosis in von Willebrand disease
Effect of fibrinolysis on bleeding phenotype in moderate and severe von Willebrand disease
Health-related quality of life among adult patients with moderate and severe von Willebrand disease
