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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
2014
Review
2014
The diagnosis and management of von Willebrand disease: a United Kingdom Haemophilia Centre Doctors Organization guideline approved by the British Committee for Standards in Haematology
The guideline group was selected to be representative of UKbased medical experts. MEDLINE and EMBASE were searched systematically… 
Review
2004
Review
2004
Treatment of von Willebrand's Disease.
N Engl J Med 2004;351:683-94. Copyright © 2004 Massachusetts Medical Society. on willebrand’s disease is an inherited bleeding… 
Review
2003
Review
2003
Von Willebrand disease type 1: a diagnosis in search of a disease.
Von Willebrand disease (VWD) type 1 is reported to be common but frequently is difficult to diagnose. Many people have… 
Review
2003
Review
2003
Animal colour vision — behavioural tests and physiological concepts
Over a century ago workers such as J. Lubbock and K. von Frisch developed behavioural criteria for establishing that non‐human… 
Highly Cited
1998
Highly Cited
1998
Pregnancy in women with von Willebrand's disease or factor XI deficiency
Objective To assess the obstetric outcome in women with von Willebrand's disease or factor XI deficiency. 
Highly Cited
1980
Highly Cited
1980
Variant von Willebrand's disease: characterization of two subtypes by analysis of multimeric composition of factor VIII/von Willebrand factor in plasma and platelets.
We have examined the multimeric composition of factor VIII/von Willebrand factor in plasma and platelet lysates by means of… 
Highly Cited
1974
Highly Cited
1974
Decreased adhesion of platelets to subendothelium in von Willebrand's disease.
Abstract The adhesion of platelets in flowing blood to the subendothelial surface of rabbit aorta was studied by a quantitative… 
Highly Cited
1972
Highly Cited
1972
The bleeding time as a screening test for evaluation of platelet function.
Abstract The value of the standardized template bleeding time was studied in 100 normal subjects and 136 patients with various… 
Highly Cited
1971
Highly Cited
1971
Immunologic differentiation of classic hemophilia (factor 8 deficiency) and von Willebrand's dissase, with observations on combined deficiencies of antihemophilic factor and proaccelerin (factor V…
Heterologous antiserum was prepared in rabbits against highly purified human antihemophilic factor (AHF, factor VIII). This… 
Highly Cited
1970
Highly Cited
1970
A quasi-static technique for MOS C-V and surface state measurements
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