Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
about
G-quadruplexes: Emerging roles in neurodegenerative diseases and the non-coding transcriptomeSpinocerebellar ataxia type 36 in the Han ChineseQuantitative evaluation of human cerebellum-dependent motor learning through prism adaptation of hand-reaching movement.Brain pathology in myotonic dystrophy: when tauopathy meets spliceopathy and RNAopathy.Another Perspective on Fasciculations: When is it not Caused by the Classic form of Amyotrophic Lateral Sclerosis or Progressive Spinal Atrophy?Spinocerebellar ataxia: relationship between phenotype and genotype - a review.Protein sequestration as a normal function of long noncoding RNAs and a pathogenic mechanism of RNAs containing nucleotide repeat expansions.Genetic and clinical analysis of spinocerebellar ataxia type 36 in Mainland China.Spinocerebellar ataxias in Venezuela: genetic epidemiology and their most likely ethnic descent.Antisense Oligonucleotides Reduce RNA Foci in Spinocerebellar Ataxia 36 Patient iPSCs.Early and selective reduction of NOP56 (Asidan) and RNA processing proteins in the motor neuron of ALS model mice.Oromandibular dystonia associated with SCA36.RNA-binding proteins in neurodegeneration: mechanisms in aggregate.Exome sequencing in a family with intellectual disability, early onset spasticity, and cerebellar atrophy detects a novel mutation in EXOSC3.Mutations in bassoon in individuals with familial and sporadic progressive supranuclear palsy-like syndrome.Inter-generational instability of inserted repeats during transmission in spinocerebellar ataxia type 31.Spinocerebellar ataxia type 36 exists in diverse populations and can be caused by a short hexanucleotide GGCCTG repeat expansion.PET and MRI detection of early and progressive neurodegeneration in spinocerebellar ataxia type 36.Motor neuron degeneration correlates with respiratory dysfunction in SCA1.FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion
P2860
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P2860
Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement (Asidan).
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年学术文章
@wuu
2012年学术文章
@zh
2012年学术文章
@zh-cn
2012年学术文章
@zh-hans
2012年学术文章
@zh-my
2012年学术文章
@zh-sg
2012年學術文章
@yue
2012年學術文章
@zh-hant
name
Clinical features of SCA36: a ...... r neuron involvement (Asidan).
@en
Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement
@nl
type
label
Clinical features of SCA36: a ...... r neuron involvement (Asidan).
@en
Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement
@nl
prefLabel
Clinical features of SCA36: a ...... r neuron involvement (Asidan).
@en
Clinical features of SCA36: a novel spinocerebellar ataxia with motor neuron involvement
@nl
P2093
P1433
P1476
Clinical features of SCA36: a ...... r neuron involvement (Asidan).
@en
P2093
Akio Koizumi
Kazuhiro Takamatsu
Koichi Okamoto
Miyuki Okamoto
Taisei Ota
Yasuhiro Manabe
Yasuyuki Ohta
Yoshio Ikeda
P304
P356
10.1212/WNL.0B013E318260436F
P407
P577
2012-06-27T00:00:00Z