"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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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 1997 | 2 | 0 | 2 |
| 2002 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2004 | 0 | 1 | 1 |
| 2006 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2014 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2020 | 0 | 1 | 1 |
| 2022 | 1 | 0 | 1 |
| 2023 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Cerebellar Ataxia" by people in Profiles.
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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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Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders. Brain. 2020 12 01; 143(12):3564-3573.
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The Initial Symptom and Motor Progression in Spinocerebellar Ataxias. Cerebellum. 2017 06; 16(3):615-622.
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The ITM2B (BRI2) gene is a target of BCL6 repression: Implications for lymphomas and neurodegenerative diseases. Biochim Biophys Acta. 2015 May; 1852(5):742-8.
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Clinical exome sequencing: the new standard in genetic diagnosis. JAMA Neurol. 2014 Oct; 71(10):1215-6.
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Cerebellar leukoencephalopathy: most likely histiocytosis-related. Neurology. 2008 Oct 21; 71(17):1361-7.
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Cerebellar ataxia with progressive improvement. Arch Neurol. 2006 Apr; 63(4):594-7.
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Interferon-gamma induced medulloblastoma in the developing cerebellum. J Neurosci. 2004 Nov 10; 24(45):10074-83.
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Novel CACNA1A mutation causes febrile episodic ataxia with interictal cerebellar deficits. Ann Neurol. 2003 Dec; 54(6):725-31.