Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pattern of Cerebral Glucose Metabolism in Spinocerebellar Ataxia 19.

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2018 nî lūn-bûn

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2018年の論文

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年学术文章

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2018年學術文章

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2018年學術文章

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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Novel Features and Abnormal Pa ...... in Spinocerebellar Ataxia 19.

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P1476

Novel Features and Abnormal Pa ...... m in Spinocerebellar Ataxia 19

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P2093

Irina Savitcheva

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José Laffita-Mesa

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Per Svenningsson

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Peter Gustavsson

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Åsa Bergendal

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P2860

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Gene structures and expression profiles of three human KCND (Kv4) potassium channels mediating A-type currents I(TO) and I(SA)

Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency

Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes

Spinocerebellar ataxia type 19/22 mutations alter heterocomplex Kv4.3 channel function and gating in a dominant manner

Cognitive impairment in SCA-19.

Metabolic characterization of spinocerebellar ataxia type 6.

A KCNC3 mutation causes a neurodevelopmental, non-progressive SCA13 subtype associated with dominant negative effects and aberrant EGFR trafficking.

The clinical importance of white matter hyperintensities on brain magnetic resonance imaging: systematic review and meta-analysis

P2888

s12311-018-0927-4

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465-476

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scholarly article

P356

10.1007/S12311-018-0927-4

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Magnus Nordenskjöld

Martin Paucar

P577

2018-08-01T00:00:00Z

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P698

29527639

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P932

6028832

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