(Q34478943)

2 August 2017

title

Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsy (English)

1 reference

2 August 2017

1 reference

Giulia Barcia

4

0 references

Catherine Chiron

object named as

Catherine Chiron

11

0 references

author name string

Rima Nabbout

1

1 reference

2 August 2017

Nicole Chemaly

2

1 reference

2 August 2017

Mathilde Chipaux

3

1 reference

2 August 2017

Charles Bouis

5

1 reference

2 August 2017

Celia Dubouch

6

1 reference

2 August 2017

Dorothee Leunen

7

1 reference

2 August 2017

Isabelle Jambaqué

8

1 reference

2 August 2017

Olivier Dulac

9

1 reference

2 August 2017

Georges Dellatolas

10

1 reference

2 August 2017

publication date

13 November 2013

1 reference

Orphanet Journal of Rare Diseases

2 August 2017

published in

1 reference

2 August 2017

volume

8

1 reference

2 August 2017

page(s)

176

1 reference

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

2 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

"Epileptic encephalopathy" of infancy and childhood: electro-clinical pictures and recent understandings

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Neuropsychological development in children with Dravet syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Cognitive and behavioral characteristics of children with Dravet syndrome: an overview

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Cerebellum can be a possible generator of progressive myoclonus

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Epileptic syndromes in infancy and childhood

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Severe myoclonic epilepsy in infancy: Dravet syndrome.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

The right brain hemisphere is dominant in human infants.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Progressive myoclonic ataxia associated with coeliac disease. The myoclonus is of cortical origin, but the pathology is in the cerebellum

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Juvenile Alzheimer's disease with myoclonus: amyloid plaques and grumose alteration in the cerebellum

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Progressive neurocognitive decline in two children with Dravet syndrome, de novo SCN1A truncations and different epileptic phenotypes.

6 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-176

Unusual consequences of status epilepticus in Dravet syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-176

Acute encephalopathy in a patient with Dravet syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-176

Early development in Dravet syndrome; visual function impairment precedes cognitive decline.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-176

Cell-type-dependent molecular composition of the axon initial segment

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1750-1172-8-176

Severe myoclonic epilepsy of infants (Dravet syndrome): natural history and neuropsychological findings.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Dravet syndrome: a study of 53 patients

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4225757

Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients

27 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24225340

12 December 2020

inferred from PubMed ID database lookup

Investigation of the role of the cerebellum in the myoclonic-like movement disorder exhibited by tottering mice

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24225340

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1186/1750-1172-8-176

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jxwe6fm3wbfgnpaxyzsaift4ie

30 July 2022

Dimensions Publication ID

1011405282

0 references

Fatcat ID

release_jxwe6fm3wbfgnpaxyzsaift4ie

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/jxwe6fm3wbfgnpaxyzsaift4ie

30 July 2022

https://api.fatcat.wiki/v0/release/jxwe6fm3wbfgnpaxyzsaift4ie

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/jxwe6fm3wbfgnpaxyzsaift4ie

1 reference

30 July 2022