Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism. - sprookjes - yvandenbroek - TriplyDB

Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.

Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.

http://www.wikidata.org/entity/Q34091178

about

Insights into the Pathology of the α3 Na(+)/K(+)-ATPase Ion Pump in Neurological Disorders; Lessons from Animal Models ATP1A3 Mutation in Adult Rapid-Onset Ataxia Cerebellar Intermittent Theta-Burst Stimulation and Motor Control Training in Individuals with Cervical Dystonia Genetic silencing of olivocerebellar synapses causes dystonia-like behaviour in mice Hypothermia-induced dystonia and abnormal cerebellar activity in a mouse model with a single disease-mutation in the sodium-potassium pump.In vivo analysis of Purkinje cell firing properties during postnatal mouse development.Aberrant Purkinje cell activity is the cause of dystonia in a shRNA-based mouse model of Rapid Onset Dystonia-Parkinsonism.A dystonia-like movement disorder with brain and spinal neuronal defects is caused by mutation of the mouse laminin β1 subunit, Lamb1.Pathogenesis of severe ataxia and tremor without the typical signs of neurodegeneration.A role for cerebellum in the hereditary dystonia DYT1.Cerebellar Synaptic Plasticity and the Credit Assignment Problem.Isolated and combined dystonia syndromes - an update on new genes and their phenotypes.Current Opinions and Areas of Consensus on the Role of the Cerebellum in Dystonia.Using the shared genetics of dystonia and ataxia to unravel their pathogenesis.Electromyographic evidence in support of a knock-in mouse model of DYT1 Dystonia.Dissecting the links between cerebellum and dystonia.The Anatomical Basis for Dystonia: The Motor Network Model.It's not just the basal ganglia: Cerebellum as a target for dystonia therapeutics.Evolving concepts in the pathogenesis of dystonia.A Case of Masticatory Dystonia Following Cerebellar Haemorrhage.PRRT2-dependent dyskinesia: cerebellar, paroxysmal and persistent.Animal Models of Tremor: Relevance to Human Tremor Disorders Oscillatory Cortical Activity in an Animal Model of Dystonia Caused by Cerebellar Dysfunction

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P2860

Abnormal high-frequency burst firing of cerebellar neurons in rapid-onset dystonia-parkinsonism.

http://www.wikidata.org/entity/Q34091178

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին 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

@zh-hk

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

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

@ast

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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type

label

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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prefLabel

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

@ast

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

@en

Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

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JNEUROSCI.1409-14.2014

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Journal of Neuroscience

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Abnormal high-frequency burst ...... d-onset dystonia-parkinsonism.

@en

P2093

D Paola Calderon

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Kamran Khodakhah

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Rachel Fremont

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P2860

Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism

Electrophysiological properties of in vitro Purkinje cell somata in mammalian cerebellar slices

De novo mutations in ATP1A3 cause alternating hemiplegia of childhood

The neural substrates of rapid-onset Dystonia-Parkinsonism.

Cerebellothalamocortical connectivity regulates penetrance in dystonia

Alternating hemiplegia of childhood-related neural and behavioural phenotypes in Na+,K+-ATPase α3 missense mutant mice.

Alternating hemiplegia of childhood: early characteristics and evolution of a neurodevelopmental syndrome

A genetic study of idiopathic focal dystonias

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene

The functional anatomy of basal ganglia disorders

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11723-11732

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scholarly article

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10.1523/JNEUROSCI.1409-14.2014

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35

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34

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2014-08-01T00:00:00Z

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265135209

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25164667

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Parkinson's disease

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4145175

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