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Spinocerebellar ataxia 36

Known as: SCA36 
 
National Institutes of Health

Related topics

Related topics

8 relations
Abnormal coordinationAutosomal dominant inheritanceCerebellar AtaxiaCerebellar atrophy
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Papers overview

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2020
2020
Cerebellar Cognitive Affective Syndrome in Costa da Morte Ataxia (SCA36)
SCA36 is an autosomal dominant spinocerebellar ataxia (SCA) affecting many families from Costa da Morte, a northwestern region of… Expand
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2018
2018
Frequency of SCA8, SCA10, SCA12, SCA36, FXTAS and C9orf72 repeat expansions in SCA patients negative for the most common SCA subtypes
BackgroundSpinocerebellar ataxia (SCA) subtypes are often caused by expansions in non-coding regions of genes like SCA8, SCA10… Expand
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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… Expand
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2017
2017
La ataxia espinocerebelosa 36 (SCA36): «Ataxia da Costa da Morte»
Resumen Introduccion-objetivos Describir la historia del descubrimiento de la SCA36 y revisar los conocimientos actuales sobre… Expand
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2017
2017
Clinical characteristics of a novel ALS/SCA crossroad mutation Asidan (SCA36) (P2.210)
Objective: In oder to clarify clinical characteristics of a novel ALS/SCA crossroad muation Asidan (SCA36). Background: A novel… Expand
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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… Expand
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2013
2013
Oromandibular dystonia associated with SCA36.
 
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2012
2012
Cognitive and affective impairments of a novel SCA/MND crossroad mutation Asidan.
BACKGROUND A variety of hereditary spinocerebellar ataxia (SCA) develops a broad spectrum of both ataxia and non-ataxia symptoms… Expand
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2012
2012
GGCCTG repeats put a hex on Purkinje cells and motor neurons in SCA36
An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat expansions.1 A group of… Expand
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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… Expand
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