Platelet-type von Willebrand disease (PT-VWD) and type 2B von Willebrand disease (2B-VWD) are rare bleeding disorders characterized by increased ristocetin-induced platelet aggregation (RIPA) at low concentrations of ristocetin. Diagnosis of either condition is not easy and the differential diagnosis between the two entities is especially challenging as evidenced by high levels of misdiagnosis of both conditions, but particularly PT-VWD. Five mutations in the GP1BA gene related to PT-VWD and less than 50 patients are currently reported worldwide. We herein describe a patient with severe bleeding symptoms, macrothrombocytopenia, mild spontaneous platelet aggregation, positive RIPA at 0.3 and 0.4 mg/mL, von Willebrand factor ristocetin cofact...
Clinical, laboratory and genetic defect of a Taiwanese family with type 213 von Willebrand disease (...
Background: von Willebrand factor propeptide (VWFpp) plays an important role in VWF multimerization ...
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other ...
Von Willebrand disease type 2B (VWD2B) expresses gain-of-function mutations that enhance binding of ...
Type 2B von Willebrand disease (vWD) is typically characterized by enhanced ristocetin-induced plate...
Interaction between the platelet glycoprotein Ib (GPIb) receptor and its adhesive ligand von Willebr...
Von Willebrand disease is an inherited bleeding disorder characterised by mucocutaneous bleeding and...
von Willebrand disease (VWD) is a common inheritable bleeding disorder caused by deficiency of von W...
Variant von Willebrand disease designated as type I New York or type Malmo is characterized by enhan...
We report on a new mutation (4337T-->C) in exon 28 of the von Willebrand factor (VWF) gene, resultin...
A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members we...
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other ...
Introduction: We characterized five patients affected with von Willebrand disease (VWD) carrying the...
thesisType 2B von Willebrand disease (vWD) and platelet-type von Willebrand disease (pt-vWD) are tw...
Abstract We describe a von Willebrand disease (VWD) variant characterized by low plasma and platele...
Clinical, laboratory and genetic defect of a Taiwanese family with type 213 von Willebrand disease (...
Background: von Willebrand factor propeptide (VWFpp) plays an important role in VWF multimerization ...
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other ...
Von Willebrand disease type 2B (VWD2B) expresses gain-of-function mutations that enhance binding of ...
Type 2B von Willebrand disease (vWD) is typically characterized by enhanced ristocetin-induced plate...
Interaction between the platelet glycoprotein Ib (GPIb) receptor and its adhesive ligand von Willebr...
Von Willebrand disease is an inherited bleeding disorder characterised by mucocutaneous bleeding and...
von Willebrand disease (VWD) is a common inheritable bleeding disorder caused by deficiency of von W...
Variant von Willebrand disease designated as type I New York or type Malmo is characterized by enhan...
We report on a new mutation (4337T-->C) in exon 28 of the von Willebrand factor (VWF) gene, resultin...
A 10-year-old male patient affected by type 2 von Willebrand disease (vWD) and his family members we...
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other ...
Introduction: We characterized five patients affected with von Willebrand disease (VWD) carrying the...
thesisType 2B von Willebrand disease (vWD) and platelet-type von Willebrand disease (pt-vWD) are tw...
Abstract We describe a von Willebrand disease (VWD) variant characterized by low plasma and platele...
Clinical, laboratory and genetic defect of a Taiwanese family with type 213 von Willebrand disease (...
Background: von Willebrand factor propeptide (VWFpp) plays an important role in VWF multimerization ...
The clinical expression of type 1 von Willebrand disease may be modified by co-inheritance of other ...