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von Willebrand Disease, Type 2N

Known as: von Willebrand Disease, Type IIN, Type IIN von Willebrand Disease, Type 2N von Willebrand Disease 
National Institutes of Health

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von Willebrand Disease, Type 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Are Iranian patients with von Willebrand disease type 2N properly differentiated from hemophilia A and do they receive appropriate treatment?
: The defect function of the von Willebrand factor (VWF) in carrying factor VIII (FVIII) leads to von Willebrand disease type 2N… 
2020
2020
Are Iranian patients with von Willebrand disease type 2N properly differentiated from hemophilia A and do they receive appropriate treatment?
: The defect function of the von Willebrand factor (VWF) in carrying factor VIII (FVIII) leads to von Willebrand disease type 2N… 
2016
2016
Introduction of transposon Tn901 iin nidulans: Preparation for cloning ir (plasmid transformation/deletion plasmid/transposable element/,
We have used the TEM fl-lactamase transposon Tn901, located on Escherichia coli plasmid pRI46, to introduce in vivo a genetic… 
Review
2013
Review
2013
SETTING THE STAGE FOR CIRCUMSTELLAR INTERACTION IN CORE-COLLAPSE SUPERNOVAE. II. WAVE-DRIVEN MASS LOSS IN SUPERNOVA PROGENITORS
Supernovae (SNe) powered by interaction with circumstellar material provide evidence for intense stellar mass loss during the… 
2013
2013
Compound heterozygous hemophilia A in a female patient and the identification of a novel missense mutation, p.Met1093Ile
Hemophilia A (HA) in females is rare. Female HA cases are often misdiagnosed as acquired HA (AHA) or as von Willebrand disease… 
2010
2010
A bright off-nuclear X-ray source: A bright off-nuclear X-ray source: a type IIn supernova, a bright ULX or a recoiling super-massive black hole in CXO J122518.6+144545
In this Paper we report the discovery of CXO J122518.6+144545; a peculiar X-ray source with a position 3.6+-0.2",off-nuclear from… 
2010
2010
von Willebrand disease type 2N: Uncovering a congenital bleeding disorder in a patient with hepatitis C, cirrhosis, and coagulopathy
Von Willebrand disease type 2N (VWD 2N) is a rare autosomal recessive bleeding disorder caused by mutations in von Willebrand… 
Review
2009
Review
2009
Seeking Core-Collapse Supernova Progenitors in Pre-Explosion Images
I summarize what we have learned about the nature of stars that ultimately explode as core-collapse supernovae from the… 
1998
1998
Diagnosis of von Willebrand disease type 2N: A simplified method for measurement of factor VIII binding to von Willebrand factor
Diagnosis of von Willebrand disease Type 2N (vWD 2N), which mimics hemophilia A and its carrier state, is important for accurate… 
Highly Cited
1996
Highly Cited
1996
Results of a Screening for von Willebrand Disease Type 2N in Patients with Suspected Haemophilia A or von Willebrand Disease Type 1
Summary A screening program for the detection of patients with von Willebrand disease type 2N (VWD 2N) was carried out in 177… 
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