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SPINOCEREBELLAR ATAXIA 31 (disorder)

Known as: SCA31, SPINOCEREBELLAR ATAXIA 31, SPINOCEREBELLAR ATAXIA, 16q22-LINKED 
National Institutes of Health

Papers overview

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2018
2018
OBJECTIVE To determine the frequency of spinocerebellar ataxia type 31 (SCA31) related mutations among patients from mainland… 
2017
2017
We report the unusual case of a 63-year-old man with spinocerebellar ataxia (SCA) type 31 who developed neuromyelitis optica… 
2017
2017
Holmes’ tremor is a low‐frequency resting and intention tremor. Here, we report a case of spinocerebellar ataxia type 31 with an… 
2015
2015
This study reports the first family in which spinocerebellar ataxia type 6 (SCA6) and spinocerebellar ataxia type 31 (SCA31… 
2014
2014
Since the discovery of spinocerebellar ataxia type 31 (SCA31) gene, we identified 6 patients whose SCA type had been unkown for a… 
2014
2014
Since the discovery of spinocerebellar ataxia type 31 (SCA31) gene, we identified 6 patients whose SCA type had been unkown for a… 
2014
2014
We evaluated atrophic sites in the brainstem and cerebellum in the patients with spinocerebellar degeneration by using voxel… 
2013
2013
Spinocerebellar ataxia type 31 (SCA31) is an autosomal dominant form of pure cerebellar ataxia that is caused by a disease… 
2011
2011
Abstract Objective: To investigate whether acoustic impairment can be one of the characteristic extracerebellar symptoms in… 
2011
2011
Autosomal dominant spinocerebellar ataxias (SCAs) are heterogeneous neurological disorders characterised by cerebellar…