Cognitive and behavioral characteristics of children with Dravet syndrome: an overview. - Wikidata - awgldk - TriplyDB

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

http://www.wikidata.org/entity/Q37861260

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Genetic background modulates impaired excitability of inhibitory neurons in a mouse model of Dravet syndrome Stiripentol : in severe myoclonic epilepsy of infancy (dravet syndrome).Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy

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Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

http://www.wikidata.org/entity/Q37861260

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on April 2011

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

@en

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

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type

label

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

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Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

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prefLabel

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

@en

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

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J.1528-1167.2011.02999.X

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Cognitive and behavioral characteristics of children with Dravet syndrome: an overview.

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Francesco Guzzetta

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P2860

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

Mutations of neuronal voltage-gated Na+ channel alpha 1 subunit gene SCN1A in core severe myoclonic epilepsy in infancy (SMEI) and in borderline SMEI (SMEB)

Reduced sodium current in Purkinje neurons from Nav1.1 mutant mice: implications for ataxia in severe myoclonic epilepsy in infancy

Reduced sodium current in GABAergic interneurons in a mouse model of severe myoclonic epilepsy in infancy

Epileptic encephalopathy.

Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy).

An internal model of a moving visual target in the lateral cerebellum.

Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients.

Neurodevelopmental evolution of West syndrome: a 2-year prospective study.

Dravet syndrome: a study of 53 patients.

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35-38

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scholarly article

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10.1111/J.1528-1167.2011.02999.X

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52 Suppl 2

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2011-04-01T00:00:00Z

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51028659

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