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Article

A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.

Neurology - 12 Jun 2007

Michelucci R, Mecarelli O, Bovo G, Bisulli F, Testoni S, Striano P, Striano S, Tinuper P, Nobile C

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 17562837
DOI: 10.1212/01.wnl.0000264932.44153.3c

Genes

LGI1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

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A de novo LGI1 mutation causing idiopathic partial epilepsy with telephone-induced seizures.PMID 17562837Read ↗

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<i>LGI1</i>mutations in temporal lobe epilepsiesSemantic proximity Read ↗

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

The LGI1 protein: molecular structure, physiological functions and disruption-related seizures.Semantic proximity Read ↗

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

A de novo mutation in an Italian sporadic patient affected by nocturnal frontal lobe epilepsy.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 ↗

Drug resistant ADLTE and recurrent partial status epilepticus with dysphasic features in a family with a novel LGI1mutation: electroclinical, genetic, and EEG/fMRI findings.Semantic proximity Read ↗

A novel SCARB2 mutation causing late-onset progressive myoclonus epilepsy.Semantic proximity Read ↗

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