(Q38025195)

27 August 2017

title

Dravet syndrome: seizure control and gait in adults with different SCN1A mutations (English)

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27 August 2017

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Jennifer J Rilstone

1

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27 August 2017

Fernando M Coelho

series ordinal

2

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27 August 2017

Berge A Minassian

series ordinal

3

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27 August 2017

Danielle M Andrade

series ordinal

4

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27 August 2017

publication date

10 July 2012

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27 August 2017

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27 August 2017

volume

53

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27 August 2017

issue

8

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27 August 2017

page(s)

1421-1428

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

27 August 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Dravet syndrome and deep brain stimulation: seizure control after 10 years of treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

A "minimal" sodium channel construct consisting of ligated S5-P-S6 segments forms a toxin-activatable ionophore

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Dravet syndrome: the long-term outcome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Severe myoclonic epilepsy of infancy (Dravet syndrome): recognition and diagnosis in adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

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.1528-1167.2012.03583.X

Effect of localization of missense mutations in SCN1A on epilepsy phenotype severity

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Genotype-phenotype correlations in a group of 15 SCN1A-mutated Italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Neuronal sodium-channel alpha1-subunit mutations in generalized epilepsy with febrile seizures plus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of Infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1528-1167.2012.03583.X

10.1111/J.1528-1167.2012.03583.X

21 January 2018

Identifiers

DOI

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27 August 2017

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