Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.
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Principal component analysis for ataxic gait using a triaxial accelerometer.A 3-year cohort study of the natural history of spinocerebellar ataxia type 6 in Japan.Vascular risk factors and clinical progression in spinocerebellar ataxiasBolivian kindred with combined spinocerebellar ataxia types 2 and 10.Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer.Coenzyme Q10 and spinocerebellar ataxias.Clinical evaluation of eye movements in spinocerebellar ataxias: a prospective multicenter studyDepression and clinical progression in spinocerebellar ataxias.Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar DegenerationDegenerative ataxias, from genes to therapies: The 2015 Cotzias Lecture.Degenerative Ataxias: challenges in clinical research.Rare neurological channelopathies--networks to study patients, pathogenesis and treatment.Spinocerebellar ataxia: relationship between phenotype and genotype - a review.Spinocerebellar Ataxia Type 2: Clinicogenetic Aspects, Mechanistic Insights, and Management Approaches.The Initial Symptom and Motor Progression in Spinocerebellar Ataxias.Dystonia and ataxia progression in spinocerebellar ataxias.Postural Tremor and Ataxia Progression in Spinocerebellar Ataxias.C9orf72 repeat expansions as genetic modifiers for depression in spinocerebellar ataxias.Polyglutamine spinocerebellar ataxias - from genes to potential treatments.Transient cerebellar alterations during development prior to obvious motor phenotype in a mouse model of spinocerebellar ataxia type 6.Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31.Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.Neurochemical abnormalities in premanifest and early spinocerebellar ataxias.Targeting potassium channels to treat cerebellar ataxia.Progression of Dysphagia in Spinocerebellar Ataxia Type 6.Current molecular insight to reveal the dynamics of CAG repeating units in spinocerebellar ataxia.A randomized controlled pilot trial of game-based training in individuals with spinocerebellar ataxia type 3.
P2860
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P2860
Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
Clinical characteristics of pa ...... ospective observational study.
@en
Clinical characteristics of pa ...... ospective observational study.
@nl
type
label
Clinical characteristics of pa ...... ospective observational study.
@en
Clinical characteristics of pa ...... ospective observational study.
@nl
prefLabel
Clinical characteristics of pa ...... ospective observational study.
@en
Clinical characteristics of pa ...... ospective observational study.
@nl
P2093
P2860
P356
P1476
Clinical characteristics of pa ...... ospective observational study.
@en
P2093
Amy Roberts Holbert
Christopher M Gomez
David Cuthbertson
George R Wilmot
Guangbin Xia
Henry L Paulson
Jeffrey P Krischer
John H Ferguson
Karla P Figueroa
Khalaf O Bushara
P2860
P2888
P356
10.1186/1750-1172-8-177
P577
2013-11-13T00:00:00Z
P5875
P6179
1005775930