"Cerebellar 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 that affect the structure or function of the cerebellum. Cardinal manifestations of cerebellar dysfunction include dysmetria, GAIT ATAXIA, and MUSCLE HYPOTONIA.
| Descriptor ID |
D002526
|
| MeSH Number(s) |
C10.228.140.252
|
| Concept/Terms |
Cerebellar Diseases- Cerebellar Diseases
- Cerebellar Disease
- Disease, Cerebellar
- Cerebellum Diseases
- Cerebellum Disease
- Disease, Cerebellum
- Cerebellar Syndromes
- Cerebellar Syndrome
- Syndrome, Cerebellar
- Cerebellar Disorders
- Cerebellar Disorder
- Disorder, Cerebellar
- Cerebellar Dysfunction
- Cerebellar Dysfunctions
- Dysfunction, Cerebellar
|
Below are MeSH descriptors whose meaning is more general than "Cerebellar Diseases".
Below are MeSH descriptors whose meaning is more specific than "Cerebellar Diseases".
This graph shows the total number of publications written about "Cerebellar Diseases" by people in this website by year, and whether "Cerebellar 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 |
|---|
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2006 | 1 | 0 | 1 |
| 2007 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 0 | 1 |
| 2011 | 3 | 0 | 3 |
| 2012 | 2 | 1 | 3 |
| 2013 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2015 | 3 | 2 | 5 |
| 2016 | 5 | 0 | 5 |
| 2017 | 2 | 0 | 2 |
| 2018 | 3 | 0 | 3 |
| 2019 | 5 | 0 | 5 |
| 2020 | 1 | 1 | 2 |
| 2021 | 2 | 0 | 2 |
| 2022 | 4 | 0 | 4 |
| 2023 | 2 | 0 | 2 |
| 2024 | 0 | 1 | 1 |
| 2025 | 4 | 0 | 4 |
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Below are the most recent publications written about "Cerebellar Diseases" by people in Profiles.
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Infratentorial Pressure Monitoring in Cerebellar Stroke: Feasibility and Prognostic Utility. Neurocrit Care. 2026 04; 44(2):578-586.
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Cerebellar Dysfunction as a Source of Dystonic Phenotypes in Mice. Cerebellum. 2023 Aug; 22(4):719-729.
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Homozygous variants in AMPD2 and COL11A1 lead to a complex phenotype of pontocerebellar hypoplasia type 9 and Stickler syndrome type 2. Am J Med Genet A. 2020 03; 182(3):557-560.
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Prenatal Cerebellar Disruptions: Neuroimaging Spectrum of Findings in Correlation with Likely Mechanisms and Etiologies of Injury. Neuroimaging Clin N Am. 2016 Aug; 26(3):359-72.
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Cerebellar cysts in children: a pattern recognition approach. Cerebellum. 2015 Jun; 14(3):308-16.
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Exome sequencing identifies a homozygous C5orf42 variant in a Turkish kindred with oral-facial-digital syndrome type VI. Am J Med Genet A. 2015 Sep; 167A(9):2132-7.
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Macrocerebellum: significance and pathogenic considerations. Cerebellum. 2012 Dec; 11(4):1026-36.
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Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI. Orphanet J Rare Dis. 2012 Jan 11; 7:4.
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Bilateral in utero cerebellar infarction. J Child Neurol. 2011 Jul; 26(7):895-9.
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"Joubert syndrome" revisited: key ocular motor signs with magnetic resonance imaging correlation. J Child Neurol. 1997 Oct; 12(7):423-30.