(Q42926147)

11 November 2017

title

A case of SUDEP in a patient with Dravet syndrome with SCN1A mutation (English)

1 reference

11 November 2017

1 reference

1 reference

2

Christian M. Korff

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20738378

23 June 2024

author name string

François Le Gal

1

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11 November 2017

Christine Monso-Hinard

3

1 reference

11 November 2017

Michael Morris

5

1 reference

11 November 2017

Alain Malafosse

6

1 reference

11 November 2017

Thomas Schmitt-Mechelke

7

1 reference

11 November 2017

Michael T. Mund

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20738378

23 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=20738378

23 June 2024

publication date

1 September 2010

1 reference

full work available at URL

11 November 2017

https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/j.1528-1167.2010.02691.x

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A20738378

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1528-1167.2010.02691.x

23 June 2024

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

https://onlinelibrary.wiley.com/doi/pdf/10.1111/j.1528-1167.2010.02691.x

23 June 2024

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

23 June 2024

1 reference

11 November 2017

volume

51

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11 November 2017

issue

9

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11 November 2017

page(s)

1915-1918

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New SCN5A mutation in a SUDEP victim with idiopathic epilepsy

11 November 2017

cites work

1

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

The SCN1A variant database: a novel research and diagnostic tool.

23 June 2024

2

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients

23 June 2024

3

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

23 June 2024

4

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

23 June 2024

6

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Two cases of sudden unexpected death in epilepsy in a GEFS+ family with an SCN1A mutation

23 June 2024

7

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A

23 June 2024

8

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Sudden unexpected death in epilepsy (SUDEP): update and reflections.

23 June 2024

9

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y

23 June 2024

10

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

What is known about the mechanisms underlying SUDEP?

23 June 2024

11

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

Inherited cardiac diseases caused by mutations in the Nav1.5 sodium channel

23 June 2024

12

1 reference

https://api.crossref.org/works/10.1111/J.1528-1167.2010.02691.X

23 June 2024

Identifiers

1 reference

11 November 2017

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