von Willebrand Disease, Type 2B

Known as: Type IIB von Willebrand Disease, Type 2B von Willebrand Disease, VWD2B 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1999-2017
02419992017

Papers overview

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2017
2017
At birth, severe thrombocytopenia without context of infection should mainly suggest neonatal alloimmune thrombocytopenia (NAIT… (More)
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2017
2017
von Willebrand disease type 2B (VWD2B) expresses gain-of-function mutations that enhance binding of an individual's von… (More)
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2017
2017
Essentials The mechanism for the auto-inhibition of von Willebrand factor (VWF) remains unclear. Hydrogen exchange of two VWF A1… (More)
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Review
2016
Review
2016
Type 2B von Willebrand disease (VWD2B) is a rare, autosomal-dominant inherited bleeding disorder, characterized by an enhanced… (More)
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Review
2016
Review
2016
A 9-month-old boy was referred to our emergency department for extensive bruising. Medical history was relevant for increased… (More)
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2013
2013
In 1980, Ruggeri et al reported a group of patients with VWD presenting a puzzling and unique feature. Although plasma VWF was… (More)
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2010
2010
von Willebrand factor (VWF) is an essential mediator of platelet adhesion to the vessel wall, but little is known about its role… (More)
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2010
2010
Type 2B von Willebrand disease (VWD2B) and platelet-type von Willebrand disease (PT-VWD) are rare bleeding disorders… (More)
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Highly Cited
2009
Highly Cited
2009
Type 2B von Willebrand disease (VWD2B) is caused by an abnormal von Willebrand factor (VWF) with increased affinity for the… (More)
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Review
2009
Review
2009
Type 2B von Willebrand disease (VWD2B) is caused by gain-of-function amino acid substitutions in the von Willebrand factor (VWF… (More)
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