 Spinocerebellar Degenerations
"Spinocerebellar Degenerations" 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.
A heterogenous group of degenerative syndromes marked by progressive cerebellar dysfunction either in isolation or combined with other neurologic manifestations. Sporadic and inherited subtypes occur. Inheritance patterns include autosomal dominant, autosomal recessive, and X-linked.
| Descriptor ID |
D013132
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| MeSH Number(s) |
C10.228.140.252.700 C10.228.854.787 C10.574.500.825 C16.320.400.780
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| Concept/Terms |
Spinocerebellar Degenerations- Spinocerebellar Degenerations
- Degeneration, Spinocerebellar
- Degenerations, Spinocerebellar
- Spinocerebellar Diseases
- Spinocerebellar Disease
- Spinocerebellar Degeneration
- Spino Cerebellar Degenerations
- Degeneration, Spino Cerebellar
- Degenerations, Spino Cerebellar
- Spino Cerebellar Degeneration
- Spino-Cerebellar Degenerations
- Degeneration, Spino-Cerebellar
- Degenerations, Spino-Cerebellar
- Spino-Cerebellar Degeneration
Marinesco-Sjogren Syndrome- Marinesco-Sjogren Syndrome
- Marinesco Sjogren Syndrome
- Syndrome, Marinesco-Sjogren
- Marinesco-Sjogren-Garland Syndrome
- Marinesco-Sjogren Syndrome-Myopathy
- Marinesco-Garland Syndrome
- Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism
Cerebellar Degenerations, Primary- Cerebellar Degenerations, Primary
- Cerebellar Degeneration, Primary
- Degeneration, Primary Cerebellar
- Degenerations, Primary Cerebellar
- Primary Cerebellar Degeneration
- Primary Cerebellar Degenerations
Corticostriatal-Spinal Degeneration- Corticostriatal-Spinal Degeneration
- Corticostriatal Spinal Degeneration
- Corticostriatal-Spinal Degenerations
- Degeneration, Corticostriatal-Spinal
- Degenerations, Corticostriatal-Spinal
Marie Cerebellar Ataxia- Marie Cerebellar Ataxia
- Cerebellar Ataxia, Marie
- Marie's Cerebellar Ataxia
- Cerebellar Ataxia, Marie's
- Maries Cerebellar Ataxia
Ataxias, Hereditary- Ataxias, Hereditary
- Ataxia, Hereditary
- Hereditary Ataxia
- Hereditary Ataxias
- Hereditary Spinocerebellar Degenerations
- Degeneration, Hereditary Spinocerebellar
- Degenerations, Hereditary Spinocerebellar
- Hereditary Spinocerebellar Degeneration
- Spinocerebellar Degeneration, Hereditary
- Spinocerebellar Degenerations, Hereditary
- Inherited Spinocerebellar Degenerations
- Degeneration, Inherited Spinocerebellar
- Degenerations, Inherited Spinocerebellar
- Inherited Spinocerebellar Degeneration
- Spinocerebellar Degeneration, Inherited
- Spinocerebellar Degenerations, Inherited
- Familial Spinocerebellar Degenerations
- Degeneration, Familial Spinocerebellar
- Degenerations, Familial Spinocerebellar
- Familial Spinocerebellar Degeneration
- Spinocerebellar Degeneration, Familial
- Spinocerebellar Degenerations, Familial
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Below are MeSH descriptors whose meaning is more general than "Spinocerebellar Degenerations".
Below are MeSH descriptors whose meaning is more specific than "Spinocerebellar Degenerations".
This graph shows the total number of publications written about "Spinocerebellar Degenerations" by people in UAMS Profiles by year, and whether "Spinocerebellar Degenerations" 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 | | 2017 | 1 | 0 | 1 | | 2006 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spinocerebellar Degenerations" by people in Profiles over the past ten years.
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Koga S, Ali S, Baker MC, Wierenga KJ, Dompenciel M, Dickson DW, Wszolek ZK. A novel clinicopathologic entity causing rapidly progressive cerebellar ataxia? Parkinsonism Relat Disord. 2022 12; 105:149-153.
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Osborn DPS, Pond HL, Mazaheri N, Dejardin J, Munn CJ, Mushref K, Cauley ES, Moroni I, Pasanisi MB, Sellars EA, Hill RS, Partlow JN, Willaert RK, Bharj J, Malamiri RA, Galehdari H, Shariati G, Maroofian R, Mora M, Swan LE, Voit T, Conti FJ, Jamshidi Y, Manzini MC. Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sj?gren Syndrome and Dystroglycanopathy. Am J Hum Genet. 2017 Mar 02; 100(3):537-545.
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