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 |
|---|
| 1996 | 4 | 0 | 4 |
| 1997 | 6 | 1 | 7 |
| 1998 | 3 | 1 | 4 |
| 1999 | 4 | 0 | 4 |
| 2002 | 0 | 1 | 1 |
| 2005 | 2 | 0 | 2 |
| 2013 | 0 | 1 | 1 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Spinocerebellar Degenerations" by people in Profiles.
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Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration. EMBO J. 2018 12 03; 37(23).
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Exome sequencing of a patient with suspected mitochondrial disease reveals a likely multigenic etiology. BMC Med Genet. 2013 Aug 16; 14:83.
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SILencing misbehaving proteins. Nat Genet. 2005 Dec; 37(12):1302-3.
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Positive selection of a pre-expansion CAG repeat of the human SCA2 gene. PLoS Genet. 2005 Sep; 1(3):e41.
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Enhanced SUMOylation in polyglutamine diseases. Biochem Biophys Res Commun. 2002 Apr 26; 293(1):307-13.
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Mutation of the E6-AP ubiquitin ligase reduces nuclear inclusion frequency while accelerating polyglutamine-induced pathology in SCA1 mice. Neuron. 1999 Dec; 24(4):879-92.
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Progress in pathogenesis studies of spinocerebellar ataxia type 1. Philos Trans R Soc Lond B Biol Sci. 1999 Jun 29; 354(1386):1079-81.
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Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy. Ann Neurol. 1999 Mar; 45(3):407-11.
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Pathogenesis of polyglutamine-induced disease: A model for SCA1. Mol Genet Metab. 1999 Mar; 66(3):172-8.
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Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. Am J Hum Genet. 1998 Oct; 63(4):1060-6.