"Spinocerebellar Ataxias" 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 group of dominantly inherited, predominately late-onset, cerebellar ataxias which have been divided into multiple subtypes based on clinical features and genetic mapping. Progressive ataxia is a central feature of these conditions, and in certain subtypes POLYNEUROPATHY; DYSARTHRIA; visual loss; and other disorders may develop. (From Joynt, Clinical Neurology, 1997, Ch65, pp 12-17; J Neuropathol Exp Neurol 1998 Jun;57(6):531-43)
| Descriptor ID |
D020754
|
| MeSH Number(s) |
C10.228.140.252.190.530 C10.228.140.252.700.700 C10.228.854.787.875 C10.574.500.825.700 C10.597.350.090.500.530 C16.320.400.780.875
|
| Concept/Terms |
Spinocerebellar Ataxias- Spinocerebellar Ataxias
- Ataxia, Spinocerebellar
- Ataxias, Spinocerebellar
- Spinocerebellar Ataxia
- Dominantly-Inherited Spinocerebellar Ataxias
- Ataxia, Dominantly-Inherited Spinocerebellar
- Ataxias, Dominantly-Inherited Spinocerebellar
- Dominantly Inherited Spinocerebellar Ataxias
- Dominantly-Inherited Spinocerebellar Ataxia
- Spinocerebellar Ataxia, Dominantly-Inherited
- Spinocerebellar Ataxias, Dominantly-Inherited
- Spinocerebellar Ataxias, Dominantly Inherited
- Spinocerebellar Atrophies
- Atrophies, Spinocerebellar
- Atrophy, Spinocerebellar
- Spinocerebellar Atrophy
Spinocerebellar Ataxia Type 2- Spinocerebellar Ataxia Type 2
- Type 2 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 2
- Ataxia 2, Spinocerebellar
- Ataxia 2s, Spinocerebellar
- Spinocerebellar Ataxia 2s
- Wadia-Swami Syndrome
- Syndrome, Wadia-Swami
- Cerebellar Degeneration with Slow Eye Movements
- Olivopontocerebellar Atrophy II
- Atrophy II, Olivopontocerebellar
- Atrophy IIs, Olivopontocerebellar
- II, Olivopontocerebellar Atrophy
- IIs, Olivopontocerebellar Atrophy
- Olivopontocerebellar Atrophy IIs
- Spinocerebellar Atrophy II
- Atrophy II, Spinocerebellar
- Atrophy IIs, Spinocerebellar
- II, Spinocerebellar Atrophy
- IIs, Spinocerebellar Atrophy
- Spinocerebellar Atrophy IIs
- Olivopontocerebellar Atrophy 2
- Atrophy 2, Olivopontocerebellar
- Atrophy 2s, Olivopontocerebellar
- Olivopontocerebellar Atrophy 2s
- Spinocerebellar Ataxia with Slow Eye Movements
- Spinocerebellar Ataxia, Cuban Type
- Spinocerebellar Atrophy 2
- Atrophy 2, Spinocerebellar
- Atrophy 2s, Spinocerebellar
- Spinocerebellar Atrophy 2s
- Spinocerebellar Degeneration with Slow Eye Movements
- Wadia Swami Syndrome
- Swami Syndrome, Wadia
- Syndrome, Wadia Swami
- Olivopontocerebellar Atrophy, Holguin Type
- Spinocerebellar Ataxia-2
Spinocerebellar Ataxia Type 7- Spinocerebellar Ataxia Type 7
- Type 7 Spinocerebellar Ataxia
- OPCA with Retinal Degeneration
- Olivopontocerebellar Atrophy III
- Atrophy III, Olivopontocerebellar
- Olivopontocerebellar Atrophy IIIs
- Autosomal Dominant Cerebellar Ataxia, Type II
- OPCA with Macular Degeneration and External Ophthalmoplegia
- Spinocerebellar Ataxia-7
- Spinocerebellar Ataxia 7
- Ataxia 7, Spinocerebellar
- Ataxia 7s, Spinocerebellar
- Spinocerebellar Ataxia 7s
Spinocerebellar Ataxia Type 5- Spinocerebellar Ataxia Type 5
- Type 5 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 5
- Ataxia 5, Spinocerebellar
- Ataxia 5s, Spinocerebellar
- Spinocerebellar Ataxia 5s
- Spinocerebellar Ataxia-5
Spinocerebellar Ataxia Type 6- Spinocerebellar Ataxia Type 6
- Type 6 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 6
- Ataxia 6, Spinocerebellar
- Ataxia 6s, Spinocerebellar
- Spinocerebellar Ataxia 6s
- Spinocerebellar Ataxia-6
Spinocerebellar Ataxia Type 1- Spinocerebellar Ataxia Type 1
- Type 1 Spinocerebellar Ataxia
- Spinocerebellar Ataxia 1
- Ataxia 1, Spinocerebellar
- Spinocerebellar Ataxia 1s
- Spinocerebellar Atrophy I
- Atrophy I, Spinocerebellar
- Spinocerebellar Atrophy Is
- SCA1
- SCA1s
- Cerebelloparenchymal Disorder I
- Cerebelloparenchymal Disorder Is
- Menzel Type OPCA
- OPCA, Menzel Type
- Schut-Haymaker Type OPCA
- OPCA, Schut-Haymaker Type
- Schut Haymaker Type OPCA
- Olivopontocerebellar Atrophy IV
- Atrophy IV, Olivopontocerebellar
- Atrophy IVs, Olivopontocerebellar
- Olivopontocerebellar Atrophy IVs
- Spinocerebellar Ataxia-1
- Olivopontocerebellar Atrophy I
- Atrophy I, Olivopontocerebellar
- Olivopontocerebellar Atrophy Is
Spinocerebellar Ataxia Type 4- Spinocerebellar Ataxia Type 4
- Spinocerebellar Ataxia 4
- Ataxia 4, Spinocerebellar
- Ataxia 4s, Spinocerebellar
- Spinocerebellar Ataxia 4s
- Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
- Spinocerebellar Ataxia-4
- Type 4 Spinocerebellar Ataxia
|
Below are MeSH descriptors whose meaning is more general than "Spinocerebellar Ataxias".
Below are MeSH descriptors whose meaning is more specific than "Spinocerebellar Ataxias".
This graph shows the total number of publications written about "Spinocerebellar Ataxias" by people in this website by year, and whether "Spinocerebellar Ataxias" 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 |
|---|
| 1999 | 1 | 0 | 1 |
| 2000 | 1 | 0 | 1 |
| 2001 | 1 | 0 | 1 |
| 2002 | 3 | 0 | 3 |
| 2003 | 0 | 1 | 1 |
| 2004 | 1 | 0 | 1 |
| 2005 | 3 | 0 | 3 |
| 2006 | 1 | 0 | 1 |
| 2007 | 1 | 0 | 1 |
| 2008 | 2 | 0 | 2 |
| 2010 | 2 | 0 | 2 |
| 2011 | 4 | 1 | 5 |
| 2012 | 2 | 0 | 2 |
| 2013 | 2 | 0 | 2 |
| 2014 | 3 | 0 | 3 |
| 2015 | 5 | 0 | 5 |
| 2016 | 3 | 0 | 3 |
| 2017 | 4 | 0 | 4 |
| 2018 | 3 | 0 | 3 |
| 2019 | 2 | 0 | 2 |
| 2020 | 4 | 0 | 4 |
| 2021 | 2 | 0 | 2 |
| 2023 | 1 | 0 | 1 |
| 2024 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Spinocerebellar Ataxias" by people in Profiles.
-
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B). Ann Neurol. 2024 Dec; 96(6):1092-1103.
-
Intermuscular Coherence in Spinocerebellar Ataxias 3 and 6: a Preliminary Study. Cerebellum. 2024 Apr; 23(2):601-608.
-
Gait Variability in Spinocerebellar Ataxia Assessed Using Wearable Inertial Sensors. Mov Disord. 2021 12; 36(12):2922-2931.
-
Genotypic Differences in Networks Supporting Regional Predictors of Speech Rate in Spinocerebellar Ataxia: Preliminary Observations. Brain Connect. 2021 08; 11(6):408-417.
-
Commentary to: "The Pathophysiology and Clinical Manifestations of Spinocerebellar Ataxia Type 6" by Rentiya et al., Cerebellum 2020;19(3):459-464). Cerebellum. 2021 06; 20(3):484-485.
-
Prodromal Spinocerebellar Ataxia Type 2 Subjects Have Quantifiable Gait and Postural Sway Deficits. Mov Disord. 2021 02; 36(2):471-480.
-
Founder Effects of Spinocerebellar Ataxias in the American Continents and the Caribbean. Cerebellum. 2020 Jun; 19(3):446-458.
-
Dysphagia in spinocerebellar ataxias type 1, 2, 3 and 6. J Neurol Sci. 2020 Aug 15; 415:116878.
-
Tremor in the Degenerative Cerebellum: Towards the Understanding of Brain Circuitry for Tremor. Cerebellum. 2019 Jun; 18(3):519-526.
-
a1ACT Is Essential for Survival and Early Cerebellar Programming in a Critical Neonatal Window. Neuron. 2019 05 22; 102(4):770-785.e7.