 Hair Diseases
"Hair 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.
Diseases affecting the orderly growth and persistence of hair.
| Descriptor ID |
D006201
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| MeSH Number(s) |
C17.800.329
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hair Diseases".
Below are MeSH descriptors whose meaning is more specific than "Hair Diseases".
This graph shows the total number of publications written about "Hair Diseases" by people in this website by year, and whether "Hair 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 |
|---|
| 2006 | 0 | 1 | 1 | | 2012 | 1 | 0 | 1 | | 2015 | 3 | 0 | 3 | | 2016 | 0 | 1 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Hair Diseases" by people in Profiles.
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Armour CM, Smith A, Hartley T, Chardon JW, Sawyer S, Schwartzentruber J, Hennekam R, Majewski J, Bulman DE, Suri M, Boycott KM. Syndrome disintegration: Exome sequencing reveals that Fitzsimmons syndrome is a co-occurrence of multiple events. Am J Med Genet A. 2016 07; 170(7):1820-5.
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Lessing JN, LaMotte ED, Moshiri AS, Mark NM. Perifollicular haemorrhage with corkscrew hair due to scurvy. Postgrad Med J. 2015 Dec; 91(1082):719-20.
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Nguyen NV, Burgos A, Prok L. Spiny Papules in an Immunosuppressed Child. Pediatr Dermatol. 2015 Nov-Dec; 32(6):e296-7.
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Ansar M, Raza SI, Lee K, Shahi S, Acharya A, Dai H, Smith JD, Shendure J, Bamshad MJ, Nickerson DA, Santos-Cortez RL, Ahmad W, Leal SM. A homozygous missense variant in type I keratin KRT25 causes autosomal recessive woolly hair. J Med Genet. 2015 Oct; 52(10):676-80.
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Snyder JR, Berk DR, Kwan A, Hudgins L, Bruckner AL. What is your diagnosis? Trichorhinophalangeal syndrome type I. Cutis. 2012 Feb; 89(2):56, 73-4.
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Wang X, Bolotin D, Chu DH, Polak L, Williams T, Fuchs E. AP-2alpha: a regulator of EGF receptor signaling and proliferation in skin epidermis. J Cell Biol. 2006 Jan 30; 172(3):409-21.
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Hassanein AM, Glanz SM, Kessler HP, Eskin TA, Liu C. beta-Catenin is expressed aberrantly in tumors expressing shadow cells. Pilomatricoma, craniopharyngioma, and calcifying odontogenic cyst. Am J Clin Pathol. 2003 Nov; 120(5):732-6.
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Yannicelli S, Hambidge KM, Picciano MF. Decreased selenium intake and low plasma selenium concentrations leading to clinical symptoms in a child with propionic acidaemia. J Inherit Metab Dis. 1992; 15(2):261-8.
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