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

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Catherine Chiron

object named as

Catherine Chiron

11

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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

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2 August 2017

publication date

13 November 2013

1 reference

Orphanet Journal of Rare Diseases

2 August 2017

published in

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2 August 2017

volume

8

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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

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

6 July 2018

1 reference

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Neuropsychological development in children with Dravet syndrome.

6 July 2018

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

6 July 2018

1 reference

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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

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

6 July 2018

1 reference

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Cerebellum can be a possible generator of progressive myoclonus

6 July 2018

1 reference

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

6 July 2018

1 reference

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Epileptic syndromes in infancy and childhood

6 July 2018

1 reference

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Idiopathic epilepsies with seizures precipitated by fever and SCN1A abnormalities.

6 July 2018

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Severe myoclonic epilepsy in infancy: Dravet syndrome.

6 July 2018

1 reference

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

6 July 2018

1 reference

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The right brain hemisphere is dominant in human infants

6 July 2018

1 reference

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

6 July 2018

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

6 July 2018

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

6 July 2018

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Unusual consequences of status epilepticus in Dravet syndrome.

21 January 2018

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Acute encephalopathy in a patient with Dravet syndrome.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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Dravet syndrome: a study of 53 patients

27 October 2018

1 reference

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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

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Fatcat ID

release_jxwe6fm3wbfgnpaxyzsaift4ie

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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