Dravet syndrome and other sodium channel-related encephalopathies.

doi:10.1111/epi.16286

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Dravet syndrome and other sodium channel-related encephalopathies.

Epilepsia - 1 Dec 2019

Guerrini Renzo, Cross Helen, Nabbout Rima, Dalla Bernardina Bernardo

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Brain Diseases
Share to Epilepsies, Myoclonic
Share to Epilepsy
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Sodium Channels

Source

Open in PubMed

Identifiers

PMID: 31904121
DOI: 10.1111/epi.16286

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dravet syndrome and other sodium channel-related encephalopathies.PMID 31904121Read ↗

Dravet syndrome: inroads into understanding epileptic encephalopathies.Semantic proximity Read ↗

Dravet Syndrome: Diagnosis and Long-Term Course.Semantic proximity Read ↗

Dravet syndrome and its mimics: Beyond SCN1A.Semantic proximity Read ↗

Dravet syndrome as part of the clinical and genetic spectrum of sodium channel epilepsies and encephalopathiesSemantic proximity Read ↗

Dravet syndrome and mitochondrial dysfunction.Semantic proximity Read ↗

Dravet syndrome: a genetic epileptic disorder.Semantic proximity Read ↗

Dravet syndrome: from electroclinical characteristics to molecular biology.Semantic proximity Read ↗

From genotype to phenotype in Dravet disease.Semantic proximity Read ↗

[Dravet syndrome as a cause of epilepsy and learning disability].Semantic proximity Read ↗

The incidence of SCN1A-related Dravet syndrome in Denmark is 1:22,000: a population-based study from 2004 to 2009.Semantic proximity Read ↗

Dravet syndrome and Dravet syndrome-like phenotype: a systematic review of the SCN1A and PCDH19 variants.Semantic proximity Read ↗

Comment: Dravet syndrome--"old gene," novel mechanism.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.