about
A SEL1L mutation links a canine progressive early-onset cerebellar ataxia to the endoplasmic reticulum-associated protein degradation (ERAD) machineryTreatment for dysphagia (swallowing difficulties) in hereditary ataxiaTreatment for dysphagia (swallowing difficulties) in hereditary ataxia syndromesCanine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24A dynamic structural model of expanded RNA CAG repeats: a refined X-ray structure and computational investigations using molecular dynamics and umbrella sampling simulations.Central ocular motor disorders, including gaze palsy and nystagmus.Computational investigation of RNA CUG repeats responsible for myotonic dystrophy 1Non-invasive detection of neurochemical changes prior to overt pathology in a mouse model of spinocerebellar ataxia type 1Brain pathology of spinocerebellar ataxias.Clinical analysis of adult-onset spinocerebellar ataxias in Thailand.Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.Clinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter studyOlfactory impairment in familial ataxias.Consensus Paper: Cerebellar Development.Cardiac involvement in hereditary ataxiasLandmark Based Shape Analysis for Cerebellar Ataxia Classification and Cerebellar Atrophy Pattern VisualizationClinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.Determination of Genotypic and Phenotypic Characteristics of Friedreich's Ataxia and Autosomal Dominant Spinocerebellar Ataxia Types 1, 2, 3, and 6Neurodegeneration as a consequence of failed mitochondrial maintenance.The Moonwalker mouse: new insights into TRPC3 function, cerebellar development, and ataxia.Treatment of cerebellar ataxia.A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2).Historical Perspectives on Ancient Greek Derived "a" Prefixed Nomenclature for Acquired Neurocognitive Impairment.Huntington's disease masquerading as spinocerebellar ataxia.Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients.Recessive spinocerebellar ataxia with paroxysmal cough attacks: a report of five cases.Novel mutations in typical and atypical genetic loci through exome sequencing in autosomal recessive cerebellar ataxia families.Ocular motor characteristics of different subtypes of spinocerebellar ataxia: distinguishing features.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Milestones in ataxia
@ast
Milestones in ataxia
@en
Milestones in ataxia
@nl
type
label
Milestones in ataxia
@ast
Milestones in ataxia
@en
Milestones in ataxia
@nl
prefLabel
Milestones in ataxia
@ast
Milestones in ataxia
@en
Milestones in ataxia
@nl
P2860
P356
P1433
P1476
Milestones in ataxia
@en
P2093
Henry Paulson
P2860
P304
P356
10.1002/MDS.23559
P407
P577
2011-05-01T00:00:00Z