"Skin Ulcer" 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.
An ULCER of the skin and underlying tissues.
| Descriptor ID |
D012883
|
| MeSH Number(s) |
C17.800.893
|
| Concept/Terms |
Skin Ulcer- Skin Ulcer
- Skin Ulcers
- Ulcer, Skin
- Ulcers, Skin
|
Below are MeSH descriptors whose meaning is more general than "Skin Ulcer".
Below are MeSH descriptors whose meaning is more specific than "Skin Ulcer".
This graph shows the total number of publications written about "Skin Ulcer" by people in this website by year, and whether "Skin Ulcer" 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 |
|---|
| 2005 | 0 | 1 | 1 |
| 2006 | 0 | 1 | 1 |
| 2010 | 1 | 0 | 1 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Skin Ulcer" by people in Profiles.
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Lysaght TB, Wooster ME, Jenkins PC, Koniaris LG. Myiasis-induced sepsis: a rare case report of Wohlfahrtiimonas chitiniclastica and Ignatzschineria indica bacteremia in the continental United States. Medicine (Baltimore). 2018 Dec; 97(52):e13627.
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Ishido T, Horita N, Takeuchi M, Kawagoe T, Shibuya E, Yamane T, Hayashi T, Meguro A, Ishido M, Minegishi K, Yoshimi R, Kirino Y, Kato S, Arimoto J, Ishigatsubo Y, Takeno M, Kurosawa M, Kaneko T, Mizuki N. Clinical manifestations of Behçet's disease depending on sex and age: results from Japanese nationwide registration. Rheumatology (Oxford). 2017 Nov 01; 56(11):1918-1927.
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Ishigatsubo Y, Ihata A, Kobayashi H, Hama M, Kirino Y, Ueda A, Takeno M, Shirai A, Ohno S. Therapeutic angiogenesis in patients with systemic sclerosis by autologous transplantation of bone-marrow-derived cells. Mod Rheumatol. 2010 Jun; 20(3):263-72.
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Topaz O, Indelman M, Chefetz I, Geiger D, Metzker A, Altschuler Y, Choder M, Bercovich D, Uitto J, Bergman R, Richard G, Sprecher E. A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis. Am J Hum Genet. 2006 Oct; 79(4):759-64.
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Li W, Dasgeb B, Phillips T, Li Y, Chen M, Garner W, Woodley DT. Wound-healing perspectives. Dermatol Clin. 2005 Apr; 23(2):181-92.