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

Precision medicine approach for in vitro modeling and computational screening of anti-epileptic drugs in pediatric epilepsy patients with SCN2A (R1629L) mutation

9 Apr 2025

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 Epilepsy research and treatment
Share to Genetics and Neurodevelopmental Disorders
Share to Genomics and Rare Diseases

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 40198980
DOI: 10.1016/j.compbiomed.2025.110100

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 9 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Precision medicine approach for in vitro modeling and computational screening of anti-epileptic drugs in pediatric epilepsy patients with SCN2A (R1629L) mutationPMID 40198980Read ↗

Personalized Medicine Using Cutting Edge Technologies for Genetic Epilepsies.Semantic proximity Read ↗

A translational multimodal machine-learning prototype predicting valproate response in epilepsy treatmentSemantic proximity Read ↗

Artificial intelligence in the assessment of epilepsy-related genetic mutations: Learned from GABAA receptors and GABA transporter 1.Semantic proximity Read ↗

From diagnosis to treatment in genetic epilepsies: Implementation of precision medicine in real-world clinical practiceSemantic proximity Read ↗

<i>In-silico</i> Drug Repurposing Pipeline for Epilepsy: Integrating Deep Learning and Structure-based ApproachesSemantic proximity Read ↗

In-silico Drug Repurposing Pipeline for Epilepsy: Integrating Deep Learning and Structure-based ApproachesSemantic proximity Read ↗

Effects of SCN1A and SCN2A polymorphisms on responsiveness to valproic acid monotherapy in epileptic children: A protocol for systematic review and meta-analysis.Semantic proximity Read ↗

A comprehensive approach to identifying repurposed drugs to treat SCN8A epilepsy.Semantic proximity Read ↗

Precision therapy in the genetic epilepsies of childhood.Semantic proximity Read ↗

Identification of new KCNT1-epilepsy drugs by <i>in silico,</i> cell and <i>Drosophila</i> modellingSemantic proximity Read ↗

Recent advances in treatment of epilepsy-related sodium channelopathiesSemantic proximity Read ↗

[The new algorithm for disease management of patients with epilepsy based on genetic research].Semantic proximity Read ↗

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