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
|
| 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.
View timeline visualization
| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 1997 | 3 | 0 | 3 |
| 1998 | 2 | 0 | 2 |
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2001 | 0 | 1 | 1 |
| 2002 | 2 | 0 | 2 |
| 2003 | 2 | 0 | 2 |
| 2004 | 2 | 0 | 2 |
| 2005 | 3 | 0 | 3 |
| 2006 | 1 | 1 | 2 |
| 2007 | 1 | 0 | 1 |
| 2008 | 2 | 0 | 2 |
| 2010 | 1 | 0 | 1 |
| 2011 | 1 | 0 | 1 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 0 | 2 |
| 2015 | 2 | 0 | 2 |
| 2016 | 1 | 1 | 2 |
| 2017 | 1 | 0 | 1 |
| 2018 | 1 | 1 | 2 |
| 2020 | 1 | 0 | 1 |
| 2021 | 1 | 0 | 1 |
| 2023 | 4 | 0 | 4 |
Below are the most recent publications written about "Spinocerebellar Degenerations" by people in Profiles.
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Late-onset hereditary ataxias with dementia. Curr Opin Neurol. 2023 08 01; 36(4):324-334.
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Spinocerebellar ataxia type 14 (SCA14) in an Argentinian family: a case report. J Med Case Rep. 2023 Apr 27; 17(1):168.
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Standards of NGS Data Sharing and Analysis in Ataxias: Recommendations by the NGS Working Group of the Ataxia Global Initiative. Cerebellum. 2024 Apr; 23(2):391-400.
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Quantitative Oculomotor Assessment in Hereditary Ataxia: Discriminatory Power, Correlation with Severity Measures, and Recommended Parameters for Specific Genotypes. Cerebellum. 2024 Feb; 23(1):121-135.
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INPP5K and SIL1 associated pathologies with overlapping clinical phenotypes converge through dysregulation of PHGDH. Brain. 2021 09 04; 144(8):2427-2442.
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The Neurodevelopmental and Motor Phenotype of SCA21 (ATX-TMEM240). J Child Neurol. 2020 12; 35(14):953-962.
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MTSS1/Src family kinase dysregulation underlies multiple inherited ataxias. Proc Natl Acad Sci U S A. 2018 12 26; 115(52):E12407-E12416.
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Loss of tubulin deglutamylase CCP1 causes infantile-onset neurodegeneration. EMBO J. 2018 12 03; 37(23).
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Impaired Feedforward Control and Enhanced Feedback Control of Speech in Patients with Cerebellar Degeneration. J Neurosci. 2017 09 20; 37(38):9249-9258.
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Genetics of Hereditary Ataxia in Scottish Terriers. J Vet Intern Med. 2017 Jul; 31(4):1132-1139.