Skip to search formSkip to main contentSkip to account menu

von Willebrand Disease

Known as: Von Willebrand Disorder, Angiohemophilias, disease von willebrand 
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as… 
National Institutes of Health

Related topics

Related topics

41 relations
1 ML Desmopressin Acetate 0.004 MG/ML InjectionANTIHEMOPHILIC FACTOR, HUMAN RECOMBINANT RESIDUES 743-1636 DELETED 1 UNT Prefilled SyringeAntihemophilic Factor, Human RecombinantAntihemophilic Factor, Human Recombinant 1 UNT Injection

Broader (2)

Blood Coagulation DisordersHereditary Diseases

Narrower (3)

Von Willebrand disease, platelet typevon Willebrand Disease, Type 2Avon Willebrand Disease, Type 2B

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2006
Review
2006
Laboratory identification of von Willebrand disease: technical and scientific perspectives.
The correct diagnosis and classification of von Willebrand disease (von Willebrand disorder; vWD) is crucial because the… 
Review
1998
Review
1998
Diagnosis of von Willebrand disease
Summary. von Willebrand disease (vWD) is a bleeding disorder caused by quantitative or qualitative defects of von Willebrand… 
1986
1986
DDAVP in type IIa von Willebrand's disease.
1-D-Amino(8-D-arginine)-vasopressin (DDAVP) infusion in three patients with type IIa von Willebrand's disease (vWD) resulted in a… 
1985
1985
Endothelial cell synthesis of von Willebrand antigen II, von Willebrand factor, and von Willebrand factor/von Willebrand antigen II complex.
von Willebrand antigen II (vW AgII) and von Willebrand factor (vWf) are immunochemically distinct proteins that are deficient in… 
Highly Cited
1982
Highly Cited
1982
Platelet-type von Willebrand's disease: characterization of a new bleeding disorder
An autosomally transmitted bleeding diathesis sharing some, but not all, features previously described in von Willebrand's… 
Highly Cited
1981
Highly Cited
1981
Stimulated Platelet Aggregation, Thromboxane B2 Formation and Platelet Sensitivity to Prostacyclin - A Critical Evaluation
Summary Platelets have been implicated in the development of atherosclerotic and thrombotic vascular diseases. Evaluation of… 
Highly Cited
1980
Highly Cited
1980
Factor VIII and Fibrinolytic Response to Deamino‐8‐d‐Argenine Vasopressin in Normal Subjects and Dissociate Response in Some Patients with Haemophilia and von Willebrand's Disease
Summary Deamino‐8‐d‐argenine vasopressin (DDAVP) was given by intravenous infusion to normal subjects, haemophiliacs and patients… 
Highly Cited
1977
Highly Cited
1977
Heterogeneity of von Willebrand's disease: Study of 40 Iranian Cases
Summary. Forty Iranian patients with von Willebrand's disease were tested for bleeding time, platelet retention to glass beads… 
Highly Cited
1976
Highly Cited
1976
Electrophoretic heterogeneity of normal factor VIII/Von Willebrand protein, and abnormal electrophoretic mobility in patients with Von Willebrand's disease.
Crossed antigen-antibody electrophoresis was used to determine the electrophoretic properties of factor VIII/Von Willebrand (F… 
Highly Cited
1973
Highly Cited
1973
Detection of heterozygotes for recessive von Willebrand's disease by the assay of antihemophilic-factor-like antigen.
Abstract Asymptomatic relatives of a girl with an extremely severe form of von Willebrand's disease who had consanguineous… 
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)