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von Willebrand Disease, Type 2

Known as: von Willebrand Disease, Type 2 [Disease/Finding], VWD2, Type 2 von Willebrand Disease 
A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants… 
National Institutes of Health

Related topics

Related topics

15 relations
Autosomal dominant inheritanceAutosomal recessive inheritanceEpistaxisIn Blood

Narrower (4)

von Willebrand Disease, Type 2Avon Willebrand Disease, Type 2Bvon Willebrand Disease, Type 2Nvon Willebrand disease type 2M

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
A novel VWF variant associated with type 2 von Willebrand disease in German Wirehaired Pointers and German Shorthaired Pointers.
Von Willebrand disease (VWD), caused by deficiency of the von Willebrand factor (VWF), is the most common bleeding disorder in… 
2014
2014
Germline de novo mutations and linkage markers vs. DNA sequencing for carrier detection in von Willebrand disease
Linkage analysis in autosomal inherited von Willebrand disease (VWD) is important to diagnose the carriers and reduce the burden… 
2011
2011
Circulating and progenitor endothelial cells are abnormal in patients with different types of von Willebrand disease and correlate with markers of angiogenesis
von Willebrand disease (VWD) is the most common inherited bleeding disorder and is caused by quantitative or qualitative defects… 
2011
2011
Functional analysis of three recombinant A1-VWF domain mutants in comparison to wild type and plasma-derived VWF facilitates subtyping in type 2 von Willebrand disease.
Highly Cited
2010
Highly Cited
2010
Evaluation of commercial von Willebrand factor collagen binding assays to assist the discrimination of types 1 and 2 von Willebrand disease
Summary This study reports on the evaluation of seven commercial von Wille-brand factor (VWF) collagen binding (VWF:CB) assays to… 
2008
2008
Current Management of von Willebrand Disease
Von Willebrand disease is the most common inherited bleeding disorder and is caused by quantitative (VWD1 and VWD3) or… 
2007
2007
Molecular Biology of von Willebrand Disease (vWD): A Study among Unrelated Pakistani Patients
2 Abstract: Von Willebrand Disease (vWD) is an autosomal dominant hereditary blood coagulation disorder that is highly variable… 
2002
2002
Inverse relationship between plasma von Willebrand factor and soluble P selectin in patients with type 1 but not type 2 von Willebrand disease
P selectin is a component of endothelial Wiebel‐Palade body membrane and platelet alpha granule membrane. Patients with von… 
1996
1996
An experimental model for testing von Willebrand factor function: successful SLA-matched crossed bone marrow transplantations between normal and von Willebrand pigs.
To assess the relative in vivo roles of von Willebrand factor (vWF) of different origins, we performed crossed bone marrow… 
1981
1981
Correction of various abnormalities in cultured porcine von Willebrand endothelial cells by inhibition of plasminogen-dependent protease activity.
Cultured aortic endothelial cells (EC) from severe homozygous von Willebrand (vWd) pigs were compared to cultured normal pig EC… 
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