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
|
| 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
|
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 | 2 | 0 | 2 |
| 2004 | 1 | 0 | 1 |
| 2006 | 2 | 0 | 2 |
| 2017 | 0 | 1 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Spinocerebellar Degenerations" by people in Profiles.
-
Weeks HM, Therrien AS, Bastian AJ. The cerebellum contributes to proprioception during motion. J Neurophysiol. 2017 08 01; 118(2):693-702.
-
Farmer JE, Deidrick KM, Gitten JC, Fennell EB, Maria BL. Parenting stress and its relationship to the behavior of children with Joubert syndrome. J Child Neurol. 2006 Feb; 21(2):163-7.
-
Braddock BA, Farmer JE, Deidrick KM, Iverson JM, Maria BL. Oromotor and communication findings in joubert syndrome: further evidence of multisystem apraxia. J Child Neurol. 2006 Feb; 21(2):160-3.
-
Parisi MA, Pinter JD, Glass IA, Field K, Maria BL, Chance PF, Mahurin RK, Cramer SC. Cerebral and cerebellar motor activation abnormalities in a subject with Joubert syndrome: functional magnetic resonance imaging (MRI) study. J Child Neurol. 2004 Mar; 19(3):214-8.
-
Koshy B, Matilla T, Burright EN, Merry DE, Fischbeck KH, Orr HT, Zoghbi HY. Spinocerebellar ataxia type-1 and spinobulbar muscular atrophy gene products interact with glyceraldehyde-3-phosphate dehydrogenase. Hum Mol Genet. 1996 Sep; 5(9):1311-8.
-
Nechiporuk T, Nechiporuk A, Guan X, Frederick R, Figueroa K, Chumakov I, Korenberg JR, de Jong PJ, Pulst SM. Identification of three new microsatellite markers in the spinocerebellar ataxia type 2 (SCA2) region and 1.2 Mb physical map. Hum Genet. 1996 Apr; 97(4):462-7.