"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)
- Spinocerebellar Ataxias
- Ataxia, Spinocerebellar
- Ataxias, Spinocerebellar
- Spinocerebellar Ataxia
- Spinocerebellar Ataxias, Dominantly-Inherited
- Spinocerebellar Ataxias, Dominantly Inherited
- Spinocerebellar Atrophies
- Atrophies, Spinocerebellar
- Atrophy, Spinocerebellar
- Spinocerebellar Atrophy
- 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 Ataxia Type 4
- Spinocerebellar Ataxia Type 4
- Spinocerebellar Ataxia-4
- Spinocerebellar Ataxia 4
- Type 4 Spinocerebellar Ataxia
- Spinocerebellar Ataxia, Autosomal Dominant, with Sensory Axonal Neuropathy
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 the URMC Research Network by year, and whether "Spinocerebellar Ataxias" was a major or minor topic of these publication.