Clinical features in a Japanese patient with autosomal dominant lateral temporal epilepsy having LGI1 mutation

Clinical Neurology

Volumn 49, Issue 4, 2009, Pages 186-190

  Fujita, Youshi ^a   Ikeda, Akio ^a   Kadono, Kentaro ^a   Kawamata, Jun ^a   Tomimoto, Hidekazu ^a   Fukuyama, Hidenao ^a   Takahashi, Ryosuke ^a  

^a KYOTO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Auditory symptom; Lateral temporal lobe epilepsy; Leucine rich glioma inactivated 1 (LGI1); Panic attack

Indexed keywords

ADULT; ANXIETY; APHASIA; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN METABOLISM; CASE REPORT; CLINICAL FEATURE; DEJA VU; ELECTROENCEPHALOGRAPHY; FEMALE; FOCAL EPILEPSY; GENE; GLUCOSE METABOLISM; GRAND MAL SEIZURE; HUMAN; JAPANESE; LGI1 GENE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; PANIC; POSITRON EMISSION TOMOGRAPHY; TEMPORAL LOBE; TEMPORAL LOBE EPILEPSY; VISUAL DISORDER; ASIAN; DIAGNOSTIC IMAGING; DOMINANT GENE; GENETICS; PEDIGREE; PSYCHOSIS;

LGI1 PROTEIN, HUMAN; PROTEIN;

ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; DIAGNOSTIC IMAGING; EPILEPSY, TEMPORAL LOBE; FEMALE; GENES, DOMINANT; HUMANS; MUTATION, MISSENSE; PEDIGREE; PROTEINS; PSYCHOTIC DISORDERS;

EID: 67649406426     PISSN: 0009918X     EISSN: None     Source Type: Journal    
DOI: 10.5692/clinicalneurol.49.186     Document Type: Article

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