"von Willebrand Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Group of hemorrhagic disorders in which the VON WILLEBRAND FACTOR is either quantitatively or qualitatively abnormal. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive. Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion.
| Descriptor ID |
D014842
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| MeSH Number(s) |
C15.378.100.100.900 C15.378.100.141.900 C15.378.140.900 C15.378.463.920 C16.320.099.920
|
| Concept/Terms |
von Willebrand Diseases- von Willebrand Diseases
- Hemophilia, Vascular
- Vascular Hemophilia
- Vascular Hemophilias
- Vascular Pseudohemophilia
- Pseudohemophilia, Vascular
- Pseudohemophilias, Vascular
- Vascular Pseudohemophilias
- Von Willebrand's Factor Deficiency
- Von Willebrand Disorder
- Disorder, Von Willebrand
- von Willebrand's Disease
- von Willebrand's Diseases
- Angiohemophilia
- Angiohemophilias
- von Willebrand Disease
|
Below are MeSH descriptors whose meaning is more general than "von Willebrand Diseases".
Below are MeSH descriptors whose meaning is more specific than "von Willebrand Diseases".
This graph shows the total number of publications written about "von Willebrand Diseases" by people in this website by year, and whether "von Willebrand Diseases" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2000 | 1 | 0 | 1 |
| 2008 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2020 | 1 | 0 | 1 |
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Below are the most recent publications written about "von Willebrand Diseases" by people in Profiles.
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Kurian CJ, Drelich DA, Rizk S. Successful liver transplant from a hemophilia A donor with no development of hemophilia A in recipient. J Thromb Haemost. 2020 04; 18(4):853-856.
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Favaloro EJ, Bonar R, Hollestelle MJ, Jennings I, Mohammed S, Meijer P, Woods T, Meiring M. Differential sensitivity of von Willebrand factor activity assays to reduced VWF molecular weight forms: A large international cross-laboratory study. Thromb Res. 2018 06; 166:96-105.
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Christman MS, Ziemba J, Casale P. Flexible ureteroscopy in children with von Willebrand disease. J Endourol. 2012 Jul; 26(7):783-6.
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Krishnan S, Siegel J, Pullen G, Hevelow M, Dampier C, Stuart M. Increased von Willebrand factor antigen and high molecular weight multimers in sickle cell disease associated with nocturnal hypoxemia. Thromb Res. 2008; 122(4):455-8.
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Diecidue R, Richard J, Spera J, Streck P. Post-traumatic hemorrhage in a patient with previously undiagnosed von Willebrand's disease. J Oral Maxillofac Surg. 2000 Mar; 58(3):332-6.
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Athreya BH, Bodurtha J, Nichols WW. Arthritis, bleeding disorder and a chromosome marker--a family study. J Rheumatol. 1987 Jun; 14(3):535-9.
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Eisenstaedt R. Blood component therapy in the treatment of platelet disorders. Semin Hematol. 1986 Jan; 23(1):1-7.