The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in detail to facilitate diagnosis during childhood and aid in the planning and assessment of treatment strategies. The objective was to evaluate the occurrence, type, and severity of bleeding in a large cohort of children with moderate and severe VWD. We included 113 children (aged 0-16 years) with Type 1 (n=60), 2 (n=44), and 3 (n=9) VWD with von Willebrand factor (VWF) antigen and/or VWF ristocetin cofactor level
von Willebrand disease is the most common inherited bleeding disorder in humans. VWD can be classifi...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The information related to the clinical spectrum of von Willebranddisease (VWD) in Chinese patientsr...
Von Willebrand disease (VWD) is the most common inherited bleeding disorder and is caused by quantit...
Von Willebrand disease (VWD) is a constitutional bleeding disorder of autosomal inheritance characte...
WOS: 000249097300013PubMed ID: 17824302Objective - Bleeding tendency of paediatric patients with con...
von Willebrand disease is the most common inherited bleeding disorder in humans. VWD can be classifi...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The bleeding phenotype of children with von Willebrand disease (VWD) needs to be characterized in de...
The information related to the clinical spectrum of von Willebranddisease (VWD) in Chinese patientsr...
Von Willebrand disease (VWD) is the most common inherited bleeding disorder and is caused by quantit...
Von Willebrand disease (VWD) is a constitutional bleeding disorder of autosomal inheritance characte...
WOS: 000249097300013PubMed ID: 17824302Objective - Bleeding tendency of paediatric patients with con...
von Willebrand disease is the most common inherited bleeding disorder in humans. VWD can be classifi...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...
Along with haemophilia A and B, von Willebrand disease (VWD) and rare bleeding disorders (RBDs) cove...