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Spinocerebellar ataxia 36
Known as:
SCA36
Â
Â
National Institutes of Health
Topic mentions per year
Topic mentions per year
2011-2017
0
2
4
2011
2017
Related topics
Related topics
8 relations
Abnormal coordination
Autosomal dominant inheritance
Cerebellar Ataxia
Cerebellar atrophy
(More)
Related mentions per year
Related mentions per year
1936-2018
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2020
Spinocerebellar ataxia 36
Autosomal dominant inheritance
Cerebellar Ataxia
Dysarthria
Gait Ataxia
Abnormal coordination
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36.
Pablo Aguiar
,
J. Pardo
,
+8 authors
J. M. Mayoral Cortés
Movement disorders : official journal of the…
2017
BACKGROUND The spinocerebellar ataxias (SCAs) form a clinically, genetically, and pathological heterogeneous group of autosomal…Â
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2017
2017
Prevalence of spinocerebellar ataxia 36 in a US population
Juliana M. Valera
,
Tatyana Diaz
,
+13 authors
Brent L. Fogel
Neurology. Genetics
2017
OBJECTIVE To assess the prevalence and clinical features of individuals affected by spinocerebellar ataxia 36 (SCA36) at a large…Â
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Review
2017
Review
2017
Spinocerebellar ataxia 36 (SCA36): «Costa da Morte ataxia».
M. Arias
,
MarÃa GarcÃa-Murias
,
M José Sobrido
Neurologia
2017
INTRODUCTION-OBJECTIVE To describe the history of the discovery of SCA36 and review knowledge of this entity, which is currently…Â
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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.
Masato Obayashi
,
Giovanni Stevanin
,
+18 authors
Alexandra Dürr
Journal of neurology, neurosurgery, and…
2015
OBJECTIVE Spinocerebellar ataxia 36 (SCA36) is an autosomal-dominant neurodegenerative disorder caused by a large (>650…Â
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Review
2015
Review
2015
[Recent advances in clinical and genetic research of spinocerebellar ataxia type 36].
Sheng Zeng
,
Bei-sha Tang
,
Jun-ling Wang
Zhonghua yi xue yi chuan xue za zhi = Zhonghua…
2015
Non-coding expansion spinocerebellar ataxias (SCAs) are a group of autosomal dominant neurodegenerative diseases characterized by…Â
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2013
2013
Assessment of swallowing in motor neuron disease and Asidan/SCA36 patients with new methods.
Nobutoshi Morimoto
,
Toru Yamashita
,
+5 authors
Koji Abe
Journal of the neurological sciences
2013
BACKGROUND We report on a unique complication of cerebellar ataxia and motor neuron disease named Asidan/SCA36 with a high…Â
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2013
2013
Oromandibular dystonia associated with SCA36.
A M Miyashiro
,
Katsunobu Sugihara
,
+7 authors
Ryuji Kaji
Movement disorders : official journal of the…
2013
Â
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Review
2012
Review
2012
[Spinocerebellar ataxia type 36 (nicknamed Asidan)].
Koji Abe
,
Yoshio Ikeda
Brain and nerve = Shinkei kenkyu no shinpo
2012
We report the phenotype of spinocerebellar ataxia type 36 (SCA36), which is a novel type of dominant cerebellar ataxia nicknamed…Â
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2012
2012
GGCCTG repeats put a hex on Purkinje cells and motor neurons in SCA36.
Tetsuo Ashizawa
,
Laura P. W. Ranum
Neurology
2012
Neurology 2012;79:302–303 An increasing number of neurologic disorders are caused by microsatellite, or simple sequence, repeat…Â
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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.
Hatasu Kobayashi
,
Koji Abe
,
+7 authors
Akio Koizumi
American journal of human genetics
2011
Autosomal-dominant spinocerebellar ataxias (SCAs) are a heterogeneous group of neurodegenerative disorders. In this study, we…Â
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