Discover Community Create You

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

Article

Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes.

Brain & development - 1 Jan 2016

Shi Xiu-Yu, Tomonoh Yuko, Wang Wen-Ze, Ishii Atsushi, Higurashi Norimichi, Kurahashi Hirokazu, Kaneko Sunao, Hirose Shinichi

Abstract excerpt

OBJECTIVE: Evaluation of the efficacy of antiepileptic drugs (AEDs) used in the treatment of Dravet syndrome (DS) with different genotypes. METHODS: Patients with DS were recruited from different tertiary hospitals. Using a direct sequencing method and Multiplex Ligation-Dependent Probe Amplification (MLPA), genetic abnormalities were assessed within the exons and flanking introns of SCN1A gene, which encodes the...

Read the complete abstract on PubMed

Topics

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

Share to Anticonvulsants
Share to Carbamazepine

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Epilepsies, Myoclonic

Share to Genotyping Techniques

Share to Infant

Share to NAV1.1 Voltage-Gated Sodium Channel

Share to Seizures

Share to Treatment Outcome

Source

Identifiers

PMID: 26183863
DOI: 10.1016/j.braindev.2015.06.008

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Efficacy of antiepileptic drugs for the treatment of Dravet syndrome with different genotypes.PMID 26183863Read ↗

Clinical and Genetic Features of Dravet Syndrome: A Prime Example of the Role of Precision Medicine in Genetic EpilepsySemantic proximity Read ↗

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

Genetic therapeutic advancements for Dravet Syndrome.Semantic proximity Read ↗

Pharmacotherapy for Dravet Syndrome.Semantic proximity Read ↗

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

SCN1A as a therapeutic target for Dravet syndrome.Semantic proximity Read ↗

Dravet syndrome in children-A population-based study.Semantic proximity Read ↗

Insights into clinical phenotypes and treatment responses in a Small cohort of Taiwanese patients with SCN1A variants: A Preliminary study.Semantic proximity Read ↗

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

The genetics of Dravet syndrome.Semantic proximity Read ↗

Impact of variant subtype on electro-clinical phenotype of Dravet syndrome- a South Indian cohort study.Semantic proximity Read ↗

[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].Semantic proximity Read ↗

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