"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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Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias. Neurology. 2025 Sep 09; 105(5):e213980.
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Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures. Am J Hum Genet. 2025 07 03; 112(7):1722-1732.
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Biallelic Loss-of-Function Variant in MINPP1 Causes Pontocerebellar Hypoplasia with Characteristic Severe Neurodevelopmental Disorder. Int J Mol Sci. 2025 May 29; 26(11).
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Cerebellar dysfunction in frontotemporal dementia: intra-cerebellar pathology and cerebellar network degeneration. J Neurol. 2025 Mar 25; 272(4):289.
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Surgical infarct volume reduction and functional outcomes in patients with ischemic cerebellar stroke: results from a multicentric retrospective study. J Neurosurg. 2024 12 01; 141(6):1681-1686.
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Necrosectomy Versus Stand-Alone Suboccipital Decompressive Craniectomy for the Management of Space-Occupying Cerebellar Infarctions-A Retrospective Multicenter Study. Neurosurgery. 2024 Mar 01; 94(3):559-566.
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WWOX P47T partial loss-of-function mutation induces epilepsy, progressive neuroinflammation, and cerebellar degeneration in mice phenocopying human SCAR12. Prog Neurobiol. 2023 04; 223:102425.
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De novo variants in EMC1 lead to neurodevelopmental delay and cerebellar degeneration and affect glial function in Drosophila. Hum Mol Genet. 2022 09 29; 31(19):3231-3244.
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Cerebellar Dysfunction as a Source of Dystonic Phenotypes in Mice. Cerebellum. 2023 Aug; 22(4):719-729.