Spinocerebellar ataxia type 6.

Spinocerebellar ataxia type 6.

Item
http://www.wikidata.org/entity/Q37914420
Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6.Torpedo formation and Purkinje cell loss: modeling their relationship in cerebellar disease.Force dysmetria in spinocerebellar ataxia 6 correlates with functional capacityImpaired Spatio-Temporal Predictive Motor Timing Associated with Spinocerebellar Ataxia Type 6Rapid Onset of Motor Deficits in a Mouse Model of Spinocerebellar Ataxia Type 6 Precedes Late Cerebellar Degeneration4-aminopyridine reverses ataxia and cerebellar firing deficiency in a mouse model of spinocerebellar ataxia type 6.Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study.The autosomal dominant spinocerebellar ataxias: emerging mechanistic themes suggest pervasive Purkinje cell vulnerability.Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature.Bicistronic CACNA1A Gene Expression in Neurons Derived from Spinocerebellar Ataxia Type 6 Patient-Induced Pluripotent Stem Cells.Targeting the CACNA1A IRES as a Treatment for Spinocerebellar Ataxia Type 6.
P2860

Spinocerebellar ataxia type 6.

Item
http://www.wikidata.org/entity/Q37914420
description
article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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artikel ilmiah
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name
Spinocerebellar ataxia type 6.
@en
Spinocerebellar ataxia type 6.
@nl
type
label
Spinocerebellar ataxia type 6.
@en
Spinocerebellar ataxia type 6.
@nl
prefLabel
Spinocerebellar ataxia type 6.
@en
Spinocerebellar ataxia type 6.
@nl
P1433
P1476
P2093
P304
P31
P356
P478
P577
P698
P356
P1433
P1476
Spinocerebellar ataxia type 6.
@en
P2093
P304
P31
P356
10.1016/B978-0-444-51892-7.00029-2
P478
P577
P698