Beyond Dravet Syndrome: Characterization of a Novel, More Severe SCN1A-Linked Epileptic Encephalopathy (Q93143687)

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scientific article published on 30 June 2019

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English	Beyond Dravet Syndrome: Characterization of a Novel, More Severe SCN1A-Linked Epileptic Encephalopathy	scientific article published on 30 June 2019

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instance of

scholarly article

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stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

title

Beyond Dravet Syndrome: Characterization of a Novel, More Severe SCN1A-Linked Epileptic Encephalopathy (English)

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stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

main subject

Dravet syndrome

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inferred from title

author name string

Veronica C Beck

series ordinal

1

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

Jacob M Hull

series ordinal

2

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

Lori L Isom

series ordinal

3

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stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

publication date

30 June 2019

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stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

published in

Epilepsy Currents

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

volume

19

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Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

issue

4

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stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

page(s)

266-268

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Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

cites work

Dynamic action potential clamp predicts functional separation in mild familial and severe de novo forms of epilepsy

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PubMed Central

reference URL

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Clinical and genetic factors predicting Dravet syndrome in infants with SCN1A mutations

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11 February 2021

Unaltered Network Activity and Interneuronal Firing During Spontaneous Cortical Dynamics In Vivo in a Mouse Model of Severe Myoclonic Epilepsy of Infancy

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Interneurons. Fast-spiking, parvalbumin⁺ GABAergic interneurons: from cellular design to microcircuit function.

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11 February 2021

A supercritical density of Na(+) channels ensures fast signaling in GABAergic interneuron axons

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11 February 2021

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

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Novel mutations mapping to the fourth sodium channel domain of Nav1.7 result in variable clinical manifestations of primary erythromelalgia

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11 February 2021

NaV1.1 channels and epilepsy

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11 February 2021

A rescuable folding defective Nav1.1 (SCN1A) sodium channel mutant causes GEFS+: common mechanism in Nav1.1 related epilepsies?

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11 February 2021

The spectrum of SCN1A-related infantile epileptic encephalopathies

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PubMed Central

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11 February 2021

Severe myoclonic epilepsy in infancy: Dravet syndrome.

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11 February 2021

Population-based study of the incidence of sudden unexplained death in epilepsy

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11 February 2021

Characterization of endogenous sodium channel gene expressed in Chinese hamster ovary cells

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11 February 2021

Identifiers

DOI

10.1177/1535759719858339

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

PMC publication ID

6891832

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

PubMed publication ID

31257984

1 reference

stated in

Europe PubMed Central

PMC publication ID

6891832

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:31257984%20AND%20SRC:MED&resulttype=core&format=json

retrieved

3 May 2020

 

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