"Scotland" 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.
No definition found.
| Descriptor ID |
D012606
|
| MeSH Number(s) |
Z01.542.363.766
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Scotland".
Below are MeSH descriptors whose meaning is more specific than "Scotland".
This graph shows the total number of publications written about "Scotland" by people in this website by year, and whether "Scotland" 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 |
|---|
| 1998 | 0 | 1 | 1 |
| 2001 | 0 | 1 | 1 |
| 2012 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
| 2024 | 0 | 1 | 1 |
| 2025 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Scotland" by people in Profiles.
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Pana TA, Mamas MA, Myint PK, Dawson DK. Sex differences in myocardial infarction care and outcomes: a longitudinal Scottish National Data-Linkage Study. Eur J Prev Cardiol. 2025 Jun 03; 32(8):696-707.
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Crichton L, Daniels K, Merrylees N, Mukanyangezi MF, Sonkwe HM, Nduwayezu R, Thomson E. Teaching Scottish medical students about global health in partnership with LMIC institutions. Does it change their views on volunteering in LMIC settings? BMC Med Educ. 2024 Jan 16; 24(1):65.
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Mamas MA, Sperrin M, Watson MC, Coutts A, Wilde K, Burton C, Kadam UT, Kwok CS, Clark AB, Murchie P, Buchan I, Hannaford PC, Myint PK. Do patients have worse outcomes in heart failure than in cancer? A primary care-based cohort study with 10-year follow-up in Scotland. Eur J Heart Fail. 2017 09; 19(9):1095-1104.
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Sandilands A, Brown SJ, Goh CS, Pohler E, Wilson NJ, Campbell LE, Miyamoto K, Kubo A, Irvine AD, Thawer-Esmail F, Munro CS, McLean WH, Kudoh J, Amagai M, Matsui T. Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin. J Invest Dermatol. 2012 May; 132(5):1507-10.
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Terrinoni A, Rugg EL, Lane EB, Melino G, Felix DH, Munro CS, McLean WH. A novel mutation in the keratin 13 gene causing oral white sponge nevus. J Dent Res. 2001 Mar; 80(3):919-23.
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Mellerio JE, Salas-Alanis JC, Talamantes ML, Horn H, Tidman MJ, Ashton GH, Eady RA, McGrath JA. A recurrent glycine substitution mutation, G2043R, in the type VII collagen gene (COL7A1) in dominant dystrophic epidermolysis bullosa. Br J Dermatol. 1998 Oct; 139(4):730-7.