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

<i>LGI1</i>mutations in temporal lobe epilepsies

13 Apr 2004

Abstract excerpt

BACKGROUND AND OBJECTIVES: A number of familial temporal lobe epilepsies (TLE) have been recently recognized. Mutations in LGI1 (leucine-rich, glioma-inactivated 1 gene) have been found in a few families with the syndrome of autosomal dominant partial epilepsy with auditory features (ADPEAF). The authors aimed to determine the spectrum of TLE phenotypes with LGI1 mutations, to study the frequency of mutations in...

Read the complete abstract on PubMed

Topics

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

Share to Autoimmune Neurological Disorders and Treatments
Share to Epilepsy research and treatment
Share to Pituitary Gland Disorders and Treatments

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 15079010
DOI: 10.1212/01.wnl.0000118213.94650.81

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

<i>LGI1</i>mutations in temporal lobe epilepsiesPMID 15079010Read ↗

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features.Semantic proximity Read ↗

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.Semantic proximity Read ↗

Novel <i>LGI1</i> mutation in a family with autosomal dominant partial epilepsy with auditory featuresSemantic proximity Read ↗

Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families.Semantic proximity Read ↗

Screening LGI1 in a cohort of 26 lateral temporal lobe epilepsy patients with auditory aura from Turkey detects a novel de novo mutation.Semantic proximity Read ↗

Autosomal dominant lateral temporal epilepsy (ADLTE): absence of chromosomal rearrangements in LGI1 gene.Semantic proximity Read ↗

Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations.Semantic proximity Read ↗

LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy.Semantic proximity Read ↗

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.Semantic proximity Read ↗

Familial mesial temporal lobe epilepsy phenotype is associated with novel LGI1 variants: A report of two families.Semantic proximity Read ↗

Autosomal dominant lateral temporal epilepsy in a family exhibiting a rare heterozygous mutation and deletion in the leucine-rich glioma inactivated 1 gene.Semantic proximity Read ↗

<i>LGI1</i> microdeletion in autosomal dominant lateral temporal epilepsySemantic proximity Read ↗

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