"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 |
|---|
| 2022 | 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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Edelman JA, Ahles TA, Prashad N, Fernbach M, Li Y, Melara RD, Root JC. The effect of visual target presence and age on antisaccade performance. J Neurophysiol. 2023 02 01; 129(2):307-319.
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Jen J, Yue Q, Nelson SF, Yu H, Litt M, Nutt J, Baloh RW. A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegia. Neurology. 1999 Jul 13; 53(1):34-7.
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Yue Q, Jen JC, Nelson SF, Baloh RW. Progressive ataxia due to a missense mutation in a calcium-channel gene. Am J Hum Genet. 1997 Nov; 61(5):1078-87.
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Baloh RW, Yue Q, Furman JM, Nelson SF. Familial episodic ataxia: clinical heterogeneity in four families linked to chromosome 19p. Ann Neurol. 1997 Jan; 41(1):8-16.