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Spinocerebellar ataxia 36

Known as: SCA36 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2011-2017
02420112017

Related topics

Related topics

8 relations
Abnormal coordinationAutosomal dominant inheritanceCerebellar AtaxiaCerebellar atrophy
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Related mentions per year

Related mentions per year

1936-2018
19401960198020002020
Spinocerebellar ataxia 36
Autosomal dominant inheritance
Cerebellar Ataxia
Dysarthria
Gait Ataxia
Abnormal coordination

Papers overview

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2017
2017
PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36.
BACKGROUND The spinocerebellar ataxias (SCAs) form a clinically, genetically, and pathological heterogeneous group of autosomal… (More)
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2017
2017
Prevalence of spinocerebellar ataxia 36 in a US population
OBJECTIVE To assess the prevalence and clinical features of individuals affected by spinocerebellar ataxia 36 (SCA36) at a large… (More)
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Review
2017
Review
2017
Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia».
INTRODUCTION-OBJECTIVE To describe the history of the discovery of SCA36 and review knowledge of this entity, which is currently… (More)
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2015
2015
Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.
OBJECTIVE Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650… (More)
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Review
2015
Review
2015
[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Non-coding expansion spinocerebellar ataxias (SCAs) are a group of autosomal dominant neurodegenerative diseases characterized by… (More)
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2013
2013
Assessment of swallowing in motor neuron disease and Asidan/SCA36 patients with new methods.
BACKGROUND We report on a unique complication of cerebellar ataxia and motor neuron disease named Asidan/SCA36 with a high… (More)
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2013
2013
Oromandibular dystonia associated with SCA36.
 
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Review
2012
Review
2012
[Spinocerebellar ataxia type 36 (nicknamed Asidan)].
We report the phenotype of spinocerebellar ataxia type 36 (SCA36), which is a novel type of dominant cerebellar ataxia nicknamed… (More)
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2012
2012
GGCCTG repeats put a hex on Purkinje cells and motor neurons in SCA36.
Neurology 2012;79:302–303 An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat… (More)
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Highly Cited
2011
Highly Cited
2011
Expansion of intronic GGCCTG hexanucleotide repeat in NOP56 causes SCA36, a type of spinocerebellar ataxia accompanied by motor neuron involvement.
Autosomal-dominant spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders. In this study, we… (More)
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