Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.

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Monitoring disease progression in spinocerebellar ataxias: implications for treatment and clinical research.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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Monitoring disease progression ...... eatment and clinical research.

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Monitoring disease progression ...... eatment and clinical research.

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label

Monitoring disease progression ...... eatment and clinical research.

@en

Monitoring disease progression ...... eatment and clinical research.

@nl

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Monitoring disease progression ...... eatment and clinical research.

@en

Monitoring disease progression ...... eatment and clinical research.

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P1476

Monitoring disease progression ...... eatment and clinical research.

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P2093

Anna Castaldo

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Caterina Mariotti

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Lidia Sarro

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Lorenzo Nanetti

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P2860

Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?

Cognitive impairments in Machado-Joseph disease

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

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.

Structural and Functional Magnetic Resonance Imaging of the Cerebellum: Considerations for Assessing Cerebellar Ataxias.

Metabolic characterization of spinocerebellar ataxia type 6.

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond.

CAG repeats determine brain atrophy in spinocerebellar ataxia 17: a VBM study.

Magnetic resonance and nuclear medicine imaging in ataxias.

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.

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919-931

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scholarly article

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10.1080/14737175.2017.1364628

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P433

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P478

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2017-08-13T00:00:00Z

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28805093

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