Spinocerebellar ataxia 36

Known as: SCA36 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2011-2017
02420112017

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
BACKGROUND The spinocerebellar ataxias (SCAs) form a clinically, genetically, and pathological heterogeneous group of autosomal… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2017
2017
OBJECTIVE To assess the prevalence and clinical features of individuals affected by spinocerebellar ataxia 36 (SCA36) at a large… (More)
  • figure 1
  • table 1
  • table 2
  • table 3
Is this relevant?
Review
2017
Review
2017
INTRODUCTION-OBJECTIVE To describe the history of the discovery of SCA36 and review knowledge of this entity, which is currently… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2015
2015
OBJECTIVE Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650… (More)
Is this relevant?
Review
2015
Review
2015
Non-coding expansion spinocerebellar ataxias (SCAs) are a group of autosomal dominant neurodegenerative diseases characterized by… (More)
Is this relevant?
2013
2013
BACKGROUND We report on a unique complication of cerebellar ataxia and motor neuron disease named Asidan/SCA36 with a high… (More)
Is this relevant?
2013
2013
 
Is this relevant?
Review
2012
Review
2012
We report the phenotype of spinocerebellar ataxia type 36 (SCA36), which is a novel type of dominant cerebellar ataxia nicknamed… (More)
Is this relevant?
2012
2012
Neurology 2012;79:302–303 An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat… (More)
Is this relevant?
Highly Cited
2011
Highly Cited
2011
Autosomal-dominant spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders. In this study, we… (More)
Is this relevant?