Degenerative Ataxias: challenges in clinical research.

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Degenerative Ataxias: challenges in clinical research.

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http://www.wikidata.org/entity/Q37572929

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2016 nî lūn-bûn

@nan

2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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2016年學術文章

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name

Degenerative Ataxias: challenges in clinical research.

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Degenerative Ataxias: challenges in clinical research.

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type

Item

label

Degenerative Ataxias: challenges in clinical research.

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Degenerative Ataxias: challenges in clinical research.

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Degenerative Ataxias: challenges in clinical research.

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Degenerative Ataxias: challenges in clinical research.

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P1476

Degenerative Ataxias: challenges in clinical research.

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Precision medicine in spinocerebellar ataxias: treatment based on common mechanisms of disease

In vivo neurometabolic profiling in patients with spinocerebellar ataxia types 1, 2, 3, and 7

Decreases in the precision of Purkinje cell pacemaking cause cerebellar dysfunction and ataxia

Auditory processing deficits in children with Friedreich ataxia.

Prevalence of ataxia in children: a systematic review

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.

Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: a cross-sectional analysis of baseline data.

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study.

Altered gene expression and DNA damage in peripheral blood cells from Friedreich's ataxia patients: cellular model of pathology.

TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.

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53-60

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10.1002/ACN3.374

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2016-11-17T00:00:00Z

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