"Alopecia" 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.
Absence of hair from areas where it is normally present.
Descriptor ID |
D000505
|
MeSH Number(s) |
C17.800.329.937.122 C23.300.035
|
Concept/Terms |
Alopecia- Alopecia
- Baldness
- Hair Loss
- Hair Losses
- Loss, Hair
- Losses, Hair
Androgenetic Alopecia- Androgenetic Alopecia
- Pattern Baldness
- Baldness, Pattern
- Androgenic Alopecia
- Alopecia, Androgenic
- Alopecias, Androgenic
- Androgenic Alopecias
- Alopecia, Androgenetic
Pseudopelade- Pseudopelade
- Alopecia Cicatrisata
- Alopecia Cicatrisatas
|
Below are MeSH descriptors whose meaning is more general than "Alopecia".
Below are MeSH descriptors whose meaning is more specific than "Alopecia".
This graph shows the total number of publications written about "Alopecia" by people in this website by year, and whether "Alopecia" 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 |
---|
2001 | 1 | 0 | 1 |
2005 | 2 | 0 | 2 |
2007 | 1 | 0 | 1 |
2008 | 2 | 0 | 2 |
2009 | 2 | 0 | 2 |
2011 | 2 | 0 | 2 |
2012 | 2 | 0 | 2 |
2013 | 5 | 0 | 5 |
2014 | 3 | 0 | 3 |
2017 | 2 | 0 | 2 |
2018 | 0 | 1 | 1 |
2019 | 2 | 0 | 2 |
2020 | 0 | 2 | 2 |
2021 | 3 | 1 | 4 |
2023 | 0 | 1 | 1 |
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Below are the most recent publications written about "Alopecia" by people in Profiles.
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Identification of a novel sporadic U2HR pathogenic variant in a patient with Marie Unna hereditary hypotrichosis. Pediatr Dermatol. 2023 May-Jun; 40(3):466-467.
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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness. PLoS One. 2021; 16(9):e0256846.
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Four hypotrichosis families with mutations in the gene LSS presenting with and without neurodevelopmental phenotypes. Am J Med Genet A. 2021 12; 185(12):3900-3904.
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Atrichia with papular lesions: a differential diagnosis of alopecia universalis not to be missed. J Eur Acad Dermatol Venereol. 2021 Nov; 35(11):e801-e803.
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Hair loss, facial dysmorphology, and skeletal alterations - a diagnostic challenge. Int J Dermatol. 2021 Oct; 60(10):e419-e421.
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Insights Into the Biology of Persistent Chemotherapy-Induced Alopecia via Genomic Approaches-An Avenue to Clinical Translation? JAMA Dermatol. 2020 09 01; 156(9):947-948.
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Loss-of-function variants in C3ORF52 result in localized autosomal recessive hypotrichosis. Genet Med. 2020 07; 22(7):1227-1234.
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Two females with hair loss. J Dtsch Dermatol Ges. 2019 08; 17(8):845-847.
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Variant PADI3 in Central Centrifugal Cicatricial Alopecia. N Engl J Med. 2019 02 28; 380(9):833-841.
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Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex. Am J Hum Genet. 2018 11 01; 103(5):777-785.