Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,217,185 papers from all fields of science
Search
Sign In
Create Free Account
von Willebrand Disease, Type 2
Known as:
von Willebrand Disease, Type 2 [Disease/Finding]
, VWD2
, Type 2 von Willebrand Disease
Expand
A subtype of von Willebrand disease that results from qualitative deficiencies of VON WILLEBRAND FACTOR. The subtype is divided into several variants…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
15 relations
Autosomal dominant inheritance
Autosomal recessive inheritance
Epistaxis
In Blood
Expand
Narrower (4)
von Willebrand Disease, Type 2A
von Willebrand Disease, Type 2B
von Willebrand Disease, Type 2N
von Willebrand disease type 2M
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Preclinical evaluation of a semi‐automated and rapid commercial electrophoresis assay for von Willebrand factor multimers
M. Pikta
,
G. Zemtsovskaja
,
+4 authors
V. Banys
Journal of clinical laboratory analysis (Print)
2018
Corpus ID: 206042457
The von Willebrand factor (VWF) multimer test is required to correctly subtype qualitative type 2 von Willebrand disease (VWD…
Expand
2015
2015
How I treat type 2 variant forms of von Willebrand disease.
A. Tosetto
,
G. Castaman
Blood
2015
Corpus ID: 26665644
Type 2 von Willebrand disease (VWD) includes a wide range of qualitative abnormalities of von Willebrand factor structure and…
Expand
Highly Cited
2012
Highly Cited
2012
Different bleeding risk in type 2A and 2M von Willebrand disease: a 2‐year prospective study in 107 patients
G. Castaman
,
A. Federici
,
+4 authors
F. Rodeghiero
Journal of Thrombosis and Haemostasis
2012
Corpus ID: 23061715
Summary. Background: Type 2A and 2M von Willebrand disease (VWD2A and VWD2M) are characterized by the presence of a…
Expand
Highly Cited
2011
Highly Cited
2011
Management of Inherited von Willebrand Disease in Italy: Results from the Retrospective Study on 1234 Patients
Augusto Federici1 , 2
,
Paolo Bucciarelli2
,
+9 authors
Pier Mannucci9
Seminars in Thrombosis and Hemostasis
2011
Corpus ID: 2788199
v VWF
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
E. Favaloro
Thrombosis and Haemostasis
2010
Corpus ID: 41829285
Summary This study reports on the evaluation of seven commercial von Wille-brand factor (VWF) collagen binding (VWF:CB) assays to…
Expand
Review
2009
Review
2009
Laboratory Diagnosis and Molecular Classification of von Willebrand Disease
A. Gadisseur
,
C. Hermans
,
Z. Berneman
,
W. Schroyens
,
H. Deckmyn
,
J. Michiels
Acta Haematologica
2009
Corpus ID: 34667858
A complete set of laboratory investigations, including bleeding time, PFA-100 closure times, factor VIII (FVIII) coagulant…
Expand
Highly Cited
2006
Highly Cited
2006
Molecular population genetics of the gene encoding the human fertilization protein zonadhesin reveals rapid adaptive evolution.
J. Gasper
,
W. Swanson
American Journal of Human Genetics
2006
Corpus ID: 21342665
A hallmark of positive selection (adaptive evolution) in protein-coding regions is a d(N)/d(S) ratio >1, where d(N) is the number…
Expand
Highly Cited
2005
Highly Cited
2005
Re-establishment of VWF-dependent Weibel-Palade bodies in VWD endothelial cells.
S. Haberichter
,
E. Merricks
,
S. Fahs
,
P. Christopherson
,
T. Nichols
,
R. Montgomery
Blood
2005
Corpus ID: 2852859
Type 3 von Willebrand disease (VWD) is a severe hemorrhagic defect in humans. We now identify the homozygous mutation in the…
Expand
2002
2002
Use of the collagen‐binding assay for von Willebrand factor in the analysis of type 2M von Willebrand disease: a comparison with the ristocetin cofactor assay
A. Riddell
,
P. Jenkins
,
I. Nitu‐Whalley
,
A. Mccraw
,
Christine A. Lee
,
S. Brown
British Journal of Haematology
2002
Corpus ID: 40676013
Summary. This study compares the utility of two functional assays for von Willebrand factor (VWF), the ristocetin cofactor assay…
Expand
Review
1997
Review
1997
Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene
D. Meyer
,
É. Fressinaud
,
+5 authors
C. Mazurier
Thrombosis and Haemostasis
1997
Corpus ID: 39718465
Type 2 vWD is defined by qualitative defects of vWF and is subdivided into four subtypes: 2N, 2B, 2A and 2M. The characterization…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE