 von Willebrand Diseases
"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
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| Concept/Terms |
von Willebrand Diseases- von Willebrand Diseases
- von Willebrand's Diseases
- von Willebrands Diseases
- von Willebrand Disease
- von Willebrand's Disease
- von Willebrands Disease
- Angiohemophilia
- Angiohemophilias
- Hemophilia, Vascular
- Vascular Hemophilia
- Vascular Hemophilias
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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.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1983 | 1 | 0 | 1 | | 2001 | 1 | 0 | 1 | | 2017 | 1 | 0 | 1 | | 2021 | 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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Quan SC, Skondra D. Case Report: Peripheral Retinal Ischemia and Retinal Neovascularization in von Willebrand Disease. Optom Vis Sci. 2021 04 01; 98(4):418-424.
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Selvam SN, Casey LJ, Bowman ML, Hawke LG, Longmore AJ, Mewburn J, Ormiston ML, Archer SL, Maurice DH, James P. Abnormal angiogenesis in blood outgrowth endothelial cells derived from von Willebrand disease patients. Blood Coagul Fibrinolysis. 2017 Oct; 28(7):521-533.
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Morrison KA, Jorde UP, Garan AR, Takayama H, Naka Y, Uriel N. Acquired von Willebrand disease during CentriMag support is associated with high prevalence of bleeding during support and after transition to heart replacement therapy. ASAIO J. 2014 Mar-Apr; 60(2):241-2.
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Uriel N, Pak SW, Jorde UP, Jude B, Susen S, Vincentelli A, Ennezat PV, Cappleman S, Naka Y, Mancini D. Acquired von Willebrand syndrome after continuous-flow mechanical device support contributes to a high prevalence of bleeding during long-term support and at the time of transplantation. J Am Coll Cardiol. 2010 Oct 05; 56(15):1207-13.
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Miller CH, Dilley A, Richardson L, Hooper WC, Evatt BL. Population differences in von Willebrand factor levels affect the diagnosis of von Willebrand disease in African-American women. Am J Hematol. 2001 Jun; 67(2):125-9.
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Verp MS, Radvany RM, Green D, Conneally PM, Patel VA, Martin AO, Simpson JL. Linkage analysis in von Willebrand disease. Clin Genet. 1983 Dec; 24(6):434-8.
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