 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 UAMS Profiles 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 |
|---|
| 2022 | 1 | 0 | 1 | | 2021 | 2 | 0 | 2 | | 2020 | 1 | 0 | 1 | | 2019 | 1 | 0 | 1 | | 2018 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2016 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2009 | 1 | 1 | 2 | | 2007 | 1 | 0 | 1 |
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Below are the most recent publications written about "Cerebellar Diseases" by people in Profiles over the past ten years.
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Toescu SM, Bruckert L, Jabarkheel R, Yecies D, Zhang M, Clark CA, Mankad K, Aquilina K, Grant GA, Feldman HM, Travis KE, Yeom KW. Spatiotemporal changes in along-tract profilometry of cerebellar peduncles in cerebellar mutism syndrome. Neuroimage Clin. 2022; 35:103000.
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Wang Y, Binkley MM, Qiao M, Pardon A, Keyrouz S, Dhar R, Ford AL. Rate of Infarct-Edema Growth on CT Predicts Need for Surgical Intervention and Clinical Outcome in Patients with Cerebellar Infarction. Neurocrit Care. 2022 06; 36(3):1011-1021.
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O'Marro MB, Nazarian SM. Abduction Variant One-and-a-Half Syndrome Due to a Massive Right Hemispheric Stroke With Uncal Herniation and Rapid Intracranial Hypertension. J Neuroophthalmol. 2021 Sep 01; 41(3):e348-e350.
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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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Wang J, Rousseau J, Kim E, Ehresmann S, Cheng YT, Duraine L, Zuo Z, Park YJ, Li-Kroeger D, Bi W, Wong LJ, Rosenfeld J, Gleeson J, Faqeih E, Alkuraya FS, Wierenga KJ, Chen J, Afenjar A, Nava C, Doummar D, Keren B, Juusola J, Grompe M, Bellen HJ, Campeau PM. Loss of Oxidation Resistance 1, OXR1, Is Associated with an Autosomal-Recessive Neurological Disease with Cerebellar Atrophy and Lysosomal Dysfunction. Am J Hum Genet. 2019 12 05; 105(6):1237-1253.
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Olson HE, Jean-Mar?ais N, Yang E, Heron D, Tatton-Brown K, van der Zwaag PA, Bijlsma EK, Krock BL, Backer E, Kamsteeg EJ, Sinnema M, Reijnders MRF, Bearden D, Begtrup A, Telegrafi A, Lunsing RJ, Burglen L, Lesca G, Cho MT, Smith LA, Sheidley BR, Moufawad El Achkar C, Pearl PL, Poduri A, Skraban CM, Tarpinian J, Nesbitt AI, Fransen van de Putte DE, Ruivenkamp CAL, Rump P, Chatron N, Sabatier I, De Bellescize J, Guibaud L, Sweetser DA, Waxler JL, Wierenga KJ, Donadieu J, Narayanan V, Ramsey KM, Nava C, Rivi?re JB, Vitobello A, Tran Mau-Them F, Philippe C, Bruel AL, Duffourd Y, Thomas L, Lelieveld SH, Schuurs-Hoeijmakers J, Brunner HG, Keren B, Thevenon J, Faivre L, Thomas G, Thauvin-Robinet C. A Recurrent De Novo PACS2 Heterozygous Missense Variant Causes Neonatal-Onset Developmental Epileptic Encephalopathy, Facial Dysmorphism, and Cerebellar Dysgenesis. Am J Hum Genet. 2018 05 03; 102(5):995-1007.
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Walker G, Limaye K, Jankowitz BT, Jadhav AP. Hypertrophic olivary degeneration after cerebellar hemorrhage. J Clin Neurosci. 2017 Sep; 43:162-164.
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Mathevosian S, Singh SR, Pu CY. Multiple System Atrophy Mistaken for Autoimmune Cerebellar Degeneration. Am J Med. 2016 Sep; 129(9):e183-4.
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