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

[Clinical, electroencephalographic and genomic characteristics of patients with epilepsy with febrile seizures plus].

Revista de neurologia - 1 Apr 2011

Cantarín-Extremera Verónica, García-Peñas Juan J, Gutiérrez-Solana Luis G, García-Fernández Marta, Ruiz-Falcó M Luz, Duat-Rodríguez Anna, López-Marín Laura

Abstract excerpt

INTRODUCTION: The most frequent mutations in the spectrum of epilepsy with febrile seizures plus are those in the voltage-dependent sodium channels or in the gamma-aminobutyric acid receptors. AIM: To describe the clinical, electroencephalographic and genomic characteristics of patients with epilepsy with febrile seizures plus and compare them with those found in the literature. PATIENTS AND METHODS: We analysed...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to Diagnosis, Differential

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Electroencephalography

Share to Epilepsy

Share to Receptors, GABA

Share to Seizures, Febrile

Share to Sodium Channels

Share to Syndrome

Source

Identifiers

PMID: 21425109

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

[Clinical, electroencephalographic and genomic characteristics of patients with epilepsy with febrile seizures plus].PMID 21425109Read ↗

Genetic epilepsies with febrile seizures plus: clinical spectrum of Polish patients with SCN1A mutation - preliminary report.Semantic proximity Read ↗

Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?Semantic proximity Read ↗

Febrile seizures, genetic (generalized) epilepsy with febrile seizures plus, and Dravet's syndrome.Semantic proximity Read ↗

Genetic epilepsy with febrile seizures plus: Refining the spectrum.Semantic proximity Read ↗

GABRG2 mutations in genetic epilepsy with febrile seizures plus: structure, roles, and molecular genetics.Semantic proximity Read ↗

[Simple febrile seizure, complex seizure, generalized epilepsy with febrile seizure plus, FIRES and new syndromes].Semantic proximity Read ↗

[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].Semantic proximity Read ↗

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes.Semantic proximity Read ↗

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

[Autosomal dominant epilepsy with febrile seizures plus].Semantic proximity Read ↗

The genetics of febrile seizures and related epilepsy syndromes.Semantic proximity Read ↗

Generalized epilepsy with febrile seizures plusSemantic proximity Read ↗

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