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
- Spino-Cerebellar Degeneration
Marinesco-Sjogren Syndrome- Marinesco-Sjogren Syndrome
- Marinesco Sjogren Syndrome
- Syndrome, Marinesco-Sjogren
- Hereditary Oligophrenic Cerebello-Lental Degeneration
- Hereditary Oligophrenic Cerebello Lental Degeneration
- Marinesco-Sjögren Syndrome
- Marinesco Sjögren Syndrome
- Syndrome, Marinesco-Sjögren
- Marinesco-Sjogren Syndrome-Hypergonadotrophic Hypogonadism
- Hypogonadism, Marinesco-Sjogren Syndrome-Hypergonadotrophic
- Marinesco Sjogren Syndrome Hypergonadotrophic Hypogonadism
- Syndrome-Hypergonadotrophic Hypogonadism, Marinesco-Sjogren
- Marinesco-Sjogren Syndrome-Myopathy
- Marinesco Sjogren Syndrome Myopathy
- Syndrome-Myopathy, Marinesco-Sjogren
- Marinesco-Sjogren-Garland Syndrome
- Marinesco Sjogren Garland Syndrome
- Syndrome, Marinesco-Sjogren-Garland
- Garland-Moorhouse Syndrome
- Garland Moorhouse Syndrome
- Syndrome, Garland-Moorhouse
- Marinesco-Garland Syndrome
- Marinesco Garland Syndrome
- Syndrome, Marinesco-Garland
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
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 this website 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 |
|---|
| 1995 | 1 | 0 | 1 |
| 1996 | 2 | 0 | 2 |
| 1997 | 1 | 0 | 1 |
| 1998 | 1 | 0 | 1 |
| 2003 | 2 | 0 | 2 |
| 2006 | 1 | 0 | 1 |
| 2009 | 1 | 0 | 1 |
| 2010 | 2 | 0 | 2 |
| 2011 | 0 | 1 | 1 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
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click here.
Below are the most recent publications written about "Spinocerebellar Degenerations" by people in Profiles.
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CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity. EMBO Mol Med. 2021 11 08; 13(11):e14095.
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Loss-of-function BK channel mutation causes impaired mitochondria and progressive cerebellar ataxia. Proc Natl Acad Sci U S A. 2020 03 17; 117(11):6023-6034.
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Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13). PLoS One. 2011 Mar 29; 6(3):e17811.
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Joubert syndrome associated with severe central sleep apnea. J Clin Sleep Med. 2010 Aug 15; 6(4):384-8.
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Longitudinal cerebral blood flow changes during speech in hereditary ataxia. Brain Lang. 2010 Jul; 114(1):43-51.
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Looking at cerebellar malformations through text-mined interactomes of mice and humans. PLoS Comput Biol. 2009 Nov; 5(11):e1000559.
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Mapping cerebral blood flow during speech production in hereditary ataxia. Neuroimage. 2006 May 15; 31(1):246-54.
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Hereditary cerebellar ataxia progressively impairs force adaptation during goal-directed arm movements. J Neurophysiol. 2004 Jan; 91(1):230-8.
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Dominantly inherited ataxias. Semin Pediatr Neurol. 2003 Sep; 10(3):210-22.
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Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission. Hum Mol Genet. 1998 Mar; 7(3):525-32.