(Q37861252)

24 August 2017

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title

The core Dravet syndrome phenotype (English)

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24 August 2017

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Charlotte Dravet

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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)

3-9

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Dravet syndrome: a study of 53 patients

24 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

The pharmacologic treatment of Dravet syndrome

21 January 2018

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

A proposed diagnostic scheme for people with epileptic seizures and with epilepsy: report of the ILAE Task Force on Classification and Terminology

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

The spectrum of SCN1A-related infantile epileptic encephalopathies

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Epidemiology of Severe Myoclonic Epilepsy of Infancy

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

An unexpected EEG course in Dravet syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Severe myoclonic epilepsy in infants--a review based on the Tokyo Women's Medical University series of 84 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Focal epilepsy resulting from a de novo SCN1A mutation

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

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

21 January 2018

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Mortality in Dravet syndrome: search for risk factors in Japanese patients

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Diagnosing idiopathic/cryptogenic epilepsy syndromes in infancy

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

Epilepsy and mental retardation limited to females: an under-recognized disorder

21 January 2018

1 reference

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Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

21 January 2018

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2011.02994.X

10.1111/J.1528-1167.2011.02994.X

21 January 2018

Identifiers

DOI

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24 August 2017

1 reference