 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.
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
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| MeSH Number(s) |
C10.228.140.252
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| 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
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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 |
|---|
| 1998 | 1 | 0 | 1 | | 2011 | 1 | 0 | 1 | | 2016 | 2 | 0 | 2 | | 2018 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 | | 2020 | 6 | 0 | 6 | | 2021 | 1 | 0 | 1 | | 2022 | 2 | 0 | 2 |
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Below are the most recent publications written about "Cerebellar Diseases" by people in Profiles.
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Chung HL, Rump P, Lu D, Glassford MR, Mok JW, Fatih J, Basal A, Marcogliese PC, Kanca O, Rapp M, Fock JM, Kamsteeg EJ, Lupski JR, Larson A, Haninbal MC, Bellen H, Harel T. 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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Moreno M, Minjarez C, Vigil J, Orfila JE, Schmidt R, Burch A, Carter DJ, Kubesh M, Yonchek J, Dietz RM, Quillinan N. Differences in hippocampal plasticity and memory outcomes in anterior versus posterior cerebellar stroke. Neurobiol Dis. 2022 06 15; 168:105701.
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Fietsam AC, Darling WG, Sosnoff JJ, Workman CD, Kamholz J, Rudroff T. Cerebellar Contributions to Motor Impairments in People with Multiple Sclerosis. Cerebellum. 2022 Dec; 21(6):1052-1060.
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Ghosh SG, Breuss MW, Schlachetzki Z, Chai G, Ross D, Stanley V, Sonmez FM, Topaloglu H, Zaki MS, Hosny H, Gad S, Gleeson JG. Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia. Eur J Hum Genet. 2021 06; 29(6):957-964.
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Mehner LC, Jung JL, Maloney JA, McCourt EA. Ocular Findings in Pontine Tegmental Cap Dysplasia. Cornea. 2020 Dec; 39(12):1516-1519.
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Chai G, Webb A, Li C, Antaki D, Lee S, Breuss MW, Lang N, Stanley V, Anzenberg P, Yang X, Marshall T, Gaffney P, Wierenga KJ, Chung BH, Tsang MH, Pais LS, Lovgren AK, VanNoy GE, Rehm HL, Mirzaa G, Leon E, Diaz J, Neumann A, Kalverda AP, Manfield IW, Parry DA, Logan CV, Johnson CA, Bonthron DT, Valleley EMA, Issa MY, Abdel-Ghafar SF, Abdel-Hamid MS, Jennings P, Zaki MS, Sheridan E, Gleeson JG. Mutations in Spliceosomal Genes PPIL1 and PRP17 Cause Neurodegenerative Pontocerebellar Hypoplasia with Microcephaly. Neuron. 2021 01 20; 109(2):241-256.e9.
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Appelhof B, Wagner M, Hoefele J, Heinze A, Roser T, Koch-Hogrebe M, Roosendaal SD, Dehghani M, Mehrjardi MYV, Torti E, Houlden H, Maroofian R, Rajabi F, Sticht H, Baas F, Wieczorek D, Jamra RA. Pontocerebellar hypoplasia due to bi-allelic variants in MINPP1. Eur J Hum Genet. 2021 03; 29(3):411-421.
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Ringman JM, Qiao Y, Garbin A, Fisher BE, Fogel B, Watari Knoell K, Chui HC, Shi Y, Rexach JE. Emotional detachment, gait ataxia, and cerebellar dysconnectivity associated with compound heterozygous mutations in the SPG7 gene. Neurocase. 2020 10; 26(5):299-304.
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Calame DJ, Xiao J, Khan MM, Hollingsworth TJ, Xue Y, Person AL, LeDoux MS. Presynaptic PRRT2 Deficiency Causes Cerebellar Dysfunction and Paroxysmal Kinesigenic Dyskinesia. Neuroscience. 2020 11 10; 448:272-286.
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Rempe T, Wang Q, Wu Q, Ballur Narayana Reddy V, Newcomer Z, Miravalle A, Mao-Draayer Y. Progressive multifocal leukoencephalopathy and granule cell neuronopathy with novel mutation flanking VP1 C-terminus in natalizumab-extended interval dosing. Neurol Neuroimmunol Neuroinflamm. 2020 05 04; 7(3).
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