(Q37861260)

24 August 2017

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title

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview (English)

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24 August 2017

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Francesco Guzzetta

1

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24 August 2017

publication date

1 April 2011

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24 August 2017

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24 August 2017

volume

52 Suppl 2

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24 August 2017

page(s)

35-38

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A long-term follow-up study of Dravet syndrome up to adulthood.

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

Dravet syndrome: a study of 53 patients.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

Early development in Dravet syndrome; visual function impairment precedes cognitive decline.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

21 January 2018

Epileptic encephalopathy

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

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)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

Progressive neurocognitive decline in two children with Dravet syndrome, de novo SCN1A truncations and different epileptic phenotypes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

Sodium channels SCN1A, SCN2A and SCN3A in familial autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02999.X

10.1111/J.1528-1167.2011.02999.X

21 January 2018

Identifiers

DOI

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24 August 2017

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