Cerebellar Diseases

"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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

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".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Cerebellar Diseases [C10.228.140.252]

Below are MeSH descriptors whose meaning is more specific than "Cerebellar Diseases".

publications

Timeline | Most Recent

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.

Bar chart showing 24 publications over 12 distinct years, with a maximum of 4 publications in 2010

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1997	2	0	2
2001	2	0	2
2003	1	0	1
2005	0	2	2
2007	0	3	3
2008	0	1	1
2010	3	1	4
2012	1	1	2
2013	2	0	2
2015	1	0	1
2017	1	1	2
2020	1	1	2

Below are the most recent publications written about "Cerebellar Diseases" by people in Profiles.

Mueller KB, Zhao D, Dowlati E, D'Antuono M, Felbaum D, Chang J, Hockstein M, Mai J, Mason B, Aulisi E, Armonda R. Intracranial hemorrhage type and same-admission mortality in patients with left ventricular assist devices. Clin Neurol Neurosurg. 2020 06; 193:105790.

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Nadkarni N, Lee YJ, Hoefen R, Alweis R. Cholangiocarcinoma Manifesting as Non-Bacterial Thrombotic Endocarditis in a Young Patient. Am J Med. 2020 08; 133(8):e396-e398.

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Tremblay S, Pai A, Richter L, Vafaei R, Potluri P, Ellegood J, Lerch JP, Goldowitz D. Systemic inflammation combined with neonatal cerebellar haemorrhage aggravates long-term structural and functional outcomes in a mouse model. Brain Behav Immun. 2017 Nov; 66:257-276.

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Tkemaladze T, Melikishvili G, Kherkheulidze V, Melikishvili A, Davitaia T. EXPANDED PHENOTYPE OF TMEM67 GENE MUTATION (CASE REPORT). Georgian Med News. 2017 Jun; (267):100-103.

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Chang RS, Leung CY, Leong HS. Bilateral Striatopallidodentate Calcinosis associated with Systemic Lupus Erythematosus: Case report and review of literature. J Neurol Sci. 2015 Nov 15; 358(1-2):518-9.

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Chalouhi N, Chitale A, Tjoumakaris S, Gonzalez LF, Theofanis T, Jabbour P. Cerebellar hemorrhage from a delayed cervical spine hardware migration. Clin Neurol Neurosurg. 2013 Sep; 115(9):1894-6.

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Ranguis SC, Chaganti JR, Winder MJ. A bilateral infratentorial neurenteric cyst. J Clin Neurosci. 2013 May; 20(5):735-8.

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Fatemi SH, Aldinger KA, Ashwood P, Bauman ML, Blaha CD, Blatt GJ, Chauhan A, Chauhan V, Dager SR, Dickson PE, Estes AM, Goldowitz D, Heck DH, Kemper TL, King BH, Martin LA, Millen KJ, Mittleman G, Mosconi MW, Persico AM, Sweeney JA, Webb SJ, Welsh JP. Consensus paper: pathological role of the cerebellum in autism. Cerebellum. 2012 Sep; 11(3):777-807.

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Pastora N, Peralta J, Canal-Fontcuberta I, Grabowska A, Pulido JS, Abelairas J, Armada F, Garcia-Alix A. Microcephaly-lymphedema-chorioretinal dysplasia associated with pachymicrogyria and atrophy of the cerebellar vermis: an integration of brain-ocular migration disorders. Ophthalmic Genet. 2012 Jun; 33(2):116-8.

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Fyfe JC, Al-Tamimi RA, Castellani RJ, Rosenstein D, Goldowitz D, Henthorn PS. Inherited neuroaxonal dystrophy in dogs causing lethal, fetal-onset motor system dysfunction and cerebellar hypoplasia. J Comp Neurol. 2010 Sep 15; 518(18):3771-84.

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