"Cerebellar Ataxia" 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.
Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)
| Descriptor ID |
D002524
|
| MeSH Number(s) |
C10.228.140.252.190 C10.597.350.090.500 C23.888.592.350.090.200
|
| Concept/Terms |
Cerebellar Ataxia- Cerebellar Ataxia
- Cerebellar Incoordination
- Cerebellar Incoordinations
- Incoordination, Cerebellar
- Incoordinations, Cerebellar
- Ataxia, Cerebellar
- Ataxias, Cerebellar
- Cerebellar Ataxias
Cerebellar Hemiataxia- Cerebellar Hemiataxia
- Cerebellar Hemiataxias
- Hemiataxia, Cerebellar
- Hemiataxias, Cerebellar
Cerebellar Dysmetria- Cerebellar Dysmetria
- Cerebellar Dysmetrias
- Dysmetria, Cerebellar
- Dysmetrias, Cerebellar
- Dysmetria
- Dysmetrias
|
Below are MeSH descriptors whose meaning is more general than "Cerebellar Ataxia".
Below are MeSH descriptors whose meaning is more specific than "Cerebellar Ataxia".
This graph shows the total number of publications written about "Cerebellar Ataxia" by people in this website by year, and whether "Cerebellar Ataxia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2005 | 1 | 0 | 1 |
| 2007 | 0 | 1 | 1 |
| 2011 | 1 | 0 | 1 |
| 2015 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
| 2019 | 2 | 1 | 3 |
| 2020 | 0 | 2 | 2 |
| 2021 | 2 | 0 | 2 |
| 2022 | 5 | 0 | 5 |
| 2023 | 1 | 0 | 1 |
| 2025 | 2 | 0 | 2 |
| 2026 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cerebellar Ataxia" by people in Profiles.
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Biallelic Novel SKOR2 Variants in Individuals With Cerebellar Hypoplasia and Intellectual Disability, Expanding the Phenotypic Spectrum of Valence-Farazi Cerebellar Ataxia Syndrome. Am J Med Genet A. 2026 Jul; 200(7):1725-1739.
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Cerebellar deep brain stimulation rescues Purkinje cell mitochondrial density in a genetic mouse model of cerebellar ataxia. Brain Res Bull. 2026 Jan; 234:111704.
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Heterozygous RAB3A variants cause cerebellar ataxia by a partial loss-of-function mechanism. Brain. 2025 Aug 01; 148(8):2812-2826.
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Cation leak through the ATP1A3 pump causes spasticity and intellectual disability. Brain. 2023 08 01; 146(8):3162-3171.
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Truncating Variants in RFC1 in Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome. Neurology. 2023 01 31; 100(5):e543-e554.
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Objective Assessment of Upper-Extremity Motor Functions in Spinocerebellar Ataxia Using Wearable Sensors. Sensors (Basel). 2022 Oct 20; 22(20).
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Home-cage behavior in the Stargazer mutant mouse. Sci Rep. 2022 07 27; 12(1):12801.
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Neuroimaging in cerebellar ataxia in childhood: A review. J Neuroimaging. 2022 09; 32(5):825-851.
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A novel de novo intronic variant in ITPR1 causes Gillespie syndrome. Am J Med Genet A. 2021 08; 185(8):2315-2324.
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Neuromodulation of the cerebellum rescues movement in a mouse model of ataxia. Nat Commun. 2021 02 26; 12(1):1295.