(Q50565779)

15 March 2018

http://europepmc.org/abstract/MED/25778844

title

The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009. (English)

1 reference

15 March 2018

http://europepmc.org/abstract/MED/25778844

0 references

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3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

author name string

Allan Bayat

series ordinal

1

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

Helle Hjalgrim

series ordinal

2

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

publication date

16 March 2015

1 reference

15 March 2018

http://europepmc.org/abstract/MED/25778844

published in

Epilepsia

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

volume

56

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

issue

4

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

page(s)

e36-9

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome

6 June 2020

cites work

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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

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Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females

21 January 2018

1 reference

Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus

21 January 2018

1 reference

A functional null mutation of SCN1B in a patient with Dravet syndrome

21 January 2018

1 reference

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome

21 January 2018

1 reference

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome

21 January 2018

1 reference

Clinical and neuropathologic findings in a case of severe myoclonic epilepsy of infancy

21 January 2018

1 reference

Hippocampal sclerosis in severe myoclonic epilepsy in infancy: a retrospective MRI study.

21 January 2018

1 reference

Brain MRI findings in severe myoclonic epilepsy in infancy and genotype-phenotype correlations.

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/EPI.12927

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25778844%20AND%20SRC:MED&resulttype=core&format=json

6 June 2020

1 reference