"Olfaction Disorders" 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.
Loss of or impaired ability to smell. This may be caused by OLFACTORY NERVE DISEASES; PARANASAL SINUS DISEASES; viral RESPIRATORY TRACT INFECTIONS; CRANIOCEREBRAL TRAUMA; SMOKING; and other conditions.
| Descriptor ID |
D000857
|
| MeSH Number(s) |
C10.597.751.600 C23.888.592.763.550
|
| Concept/Terms |
Cacosmia- Cacosmia
- Cacosmias
- Dysosmia
- Dysosmias
|
Below are MeSH descriptors whose meaning is more general than "Olfaction Disorders".
Below are MeSH descriptors whose meaning is more specific than "Olfaction Disorders".
This graph shows the total number of publications written about "Olfaction Disorders" by people in this website by year, and whether "Olfaction Disorders" was a major or minor topic of these publications.
To see the data from this visualization as text,
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2004 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2024 | 1 | 1 | 2 |
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Below are the most recent publications written about "Olfaction Disorders" by people in Profiles.
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Olfactory deficit and gastrointestinal dysfunction precede motor abnormalities in alpha-Synuclein G51D knock-in mice. Proc Natl Acad Sci U S A. 2024 09 24; 121(39):e2406479121.
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Olfactory Dysfunction and Depression Trajectories in Community-Dwelling Older Adults. J Gerontol A Biol Sci Med Sci. 2024 01 01; 79(1).
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A systematic-review of olfactory deficits in neurodevelopmental disorders: From mouse to human. Neurosci Biobehav Rev. 2021 06; 125:110-121.
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Olfactory reference syndrome symptoms in Chinese university students: Phenomenology, associated impairment, and clinical correlates. Compr Psychiatry. 2018 10; 86:91-95.
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Anosmia and Ageusia in Parkinson's Disease. Int Rev Neurobiol. 2017; 133:541-556.
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Marked olfactory impairment in idiopathic intracranial hypertension. J Neurol Neurosurg Psychiatry. 2014 Sep; 85(9):959-64.
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Defects in neural stem cell proliferation and olfaction in Chd7 deficient mice indicate a mechanism for hyposmia in human CHARGE syndrome. Hum Mol Genet. 2009 Jun 01; 18(11):1909-23.
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Brain perfusion single photon emission computed tomography findings in patients with posttraumatic anosmia and comparison with radiological imaging. Am J Rhinol. 2006 Nov-Dec; 20(6):577-81.
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Loss of BBS proteins causes anosmia in humans and defects in olfactory cilia structure and function in the mouse. Nat Genet. 2004 Sep; 36(9):994-8.
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Brief report: intragenic deletion of the KALIG-1 gene in Kallmann's syndrome. N Engl J Med. 1992 Jun 25; 326(26):1752-5.