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von Willebrand Disease, Type 1

Known as: von Willebrand Disease, Type 1 [Disease/Finding], Type 1 von Willebrand Disease, VON WILLEBRAND DISEASE, TYPE I 
A subtype of von Willebrand disease that results from a partial deficiency of VON WILLEBRAND FACTOR.
National Institutes of Health

Related topics

Related topics

10 relations
Autosomal dominant inheritanceEpistaxisIn BloodMenorrhagia

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Critical Importance Of VWF Propeptide (VWFpp) In The Diagnosis Of Type 1 Von Willebrand Disease (VWD)
Type 1 VWD is the most common form of VWD and is characterized by quantitative deficiency of VWF. Mechanisms causing type 1 VWD… 
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… 
2010
2010
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort
Type 1 von Willebrand disease (VWD) results from a partial quantitative deficiency of plasma von Willebrand factor (VWF). Three… 
2007
2007
Catamenial hemoptysis from endobronchial endometriosis in a child with type 1 von Willebrand disease
Catamenial hemoptysis is a rare condition characterized by cyclic pulmonary hemorrhage, synchronous with menses and associated… 
2000
2000
Pregnancy in Women with Type 1 von Willebrand Disease Caused by Heterozygosity for von Willebrand Factor Mutation C1130F
Pregnancy in Women with Type 1 von Willebrand Disease Caused by Heterozygosity for von Willebrand Factor Mutation C1130F - 
1999
1999
Mutations in von Willebrand Factor Multimerization Domains Are not a Common Cause of Classical Type 1 von Willebrand Disease
Summary Type 1 von Willebrand disease (vWD) is an autosomal dominant bleeding disorder of variable penetrance. It is… 
1998
1998
Comparative mapping of distal murine chromosome 11 and human 17q21.3 in a region containing a modifying locus for murine plasma von Willebrand factor level.
Type 1 von Willebrand disease (VWD) is a common inherited disorder characterized by mild to moderate bleeding and reduced levels… 
1996
1996
Combined Hereditary Disorders of Haemophilia B Leyden (-6 G → A) and Type 1 von Willebrand Disease
Summary Multiple coagulation disorders are unusual. We report here a combination of haemophilia B Leyden with type 1 von… 
1994
1994
A novel case of compound heterozygosity with “Normandy”/type I von Willebrand disease (vWD). Direct demonstration of the segregation of one allele with a defective expression at the mRNA level…
We report the case of a family with type I von Willebrand disease (vWD), characterized by a quantitative defect in von Willebrand… 
1993
1993
Functional Analysis of the Arg91GIn Substitution in the Factor VIII Binding Domain of von Willebrand Factor Demonstrates Variable Phenotypic Expression
Summary An Arg91Gln substitution in the mature von Willebrand factor (vWF) has been associated with defective binding of vWF to… 
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