Autosomal dominant cerebellar ataxias: a systematic review of clinical features. - Wikidata - awgldk - TriplyDB

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

http://www.wikidata.org/entity/Q34417063

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Pain in Neurodegenerative Disease: Current Knowledge and Future Perspectives Ataxia.Clinical and neuroradiological features of spinocerebellar ataxia 38 (SCA38)Principal component analysis for ataxic gait using a triaxial accelerometer.Clinical assessment of standing and gait in ataxic patients using a triaxial accelerometer.Pseudocyst of the auricle in patients with movement disorders: report of two patients with ataxia-associated auricular pseudocysts.Cerebellar Dysfunction and Ataxia in Patients with Epilepsy: Coincidence, Consequence, or Cause?Induced pluripotent stem cell technology for modelling and therapy of cerebellar ataxia.Non-Ataxic Presenting Symptoms of Dominant Ataxias.Kv3.3 potassium channels and spinocerebellar ataxia.Unusual tremor syndromes: know in order to recognise.Spinocerebellar ataxia 15: A phenotypic review and expansion.Ataxia in children: early recognition and clinical evaluation.Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature.Oxidative Stress in Neurodegenerative Diseases: From Molecular Mechanisms to Clinical Applications ITPR1 gene p.Val1553Met mutation in Russian family with mild Spinocerebellar ataxia.Clinical and genetic analysis of spinocerebellar ataxia type 7 (SCA7) in Zambian families.Kv3 Channels: Enablers of Rapid Firing, Neurotransmitter Release, and Neuronal Endurance.The diagnosis of dementias: a practical tool not to miss rare causes.Spinocerebellar Ataxia 27: A Review and Characterization of an Evolving Phenotype.[Genetics of tremor].Evaluation of Various Movement Disorders in Patients of Genetically Proven Spinocerebellar Ataxia: A Study from a Tertiary Care Center in Northern India.Roles of Post-translational Modifications in Spinocerebellar Ataxias Genetic Dystonia-ataxia Syndromes: Clinical Spectrum, Diagnostic Approach, and Treatment Options Voxel-based meta-analysis of gray and white matter volume abnormalities in spinocerebellar ataxia type 2

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P2860

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

http://www.wikidata.org/entity/Q34417063

description

2014 nî lūn-bûn

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2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի փետրվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

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Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

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Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

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type

label

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

@ast

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

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Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

@nl

prefLabel

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

@ast

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

@en

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

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European Journal of Neurology

P1476

Autosomal dominant cerebellar ataxias: a systematic review of clinical features.

@en

P2093

A Cammarota

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D Cerquetti

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H Hawkes

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J Balej

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L Doldan

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P2860

The wide spectrum of spinocerebellar ataxias (SCAs)

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.

Similarities and differences in the phenotype, genotype and pathogenesis of different spinocerebellar ataxias.

Update on degenerative ataxias.

The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Tutorial in biostatistics: sample sizes for parallel group clinical trials with binary data.

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.

Yet another spinocerebellar ataxia--will it ever end?

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study.

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.

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607-615

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scholarly article

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10.1111/ENE.12350

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4

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21

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