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

A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.

Archives of neurology - 1 Nov 2003

Cho Yong-Won, Motamedi Gholam K, Laufenberg Iris, Sohn Sung-Il, Lim Jeong-Geun, Lee Hyung, Yi Sang-Doe, Lee Ju-Hwa, Kim Dae-Kwang, Reba Richard, Gaillard William D, Theodore William H, Lesser Ronald P, Steinlein Ortrud K

Abstract excerpt

BACKGROUND: A Korean family had distinctive clinical and neuroimaging features and carried the same genetic mutation that was found in a previously described Japanese kindred with autosomal dominant nocturnal frontal lobe epilepsy. OBJECTIVE: To describe the first Korean family with autosomal dom...

Read the complete abstract on PubMed

Topics

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

Share to Electroencephalography
Share to Epilepsy, Frontal Lobe

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intellectual Disability

Share to Neuropsychological Tests

Share to Penetrance

Share to Receptors, Nicotinic

Share to Tomography, Emission-Computed

Source

Identifiers

PMID: 14623738
DOI: 10.1001/archneur.60.11.1625

Genes

CHRNA4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-14623738-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A Korean kindred with autosomal dominant nocturnal frontal lobe epilepsy and mental retardation.PMID 14623738Read ↗

Electroclinical picture of autosomal dominant nocturnal frontal lobe epilepsy in a Japanese family.Semantic proximity Read ↗

Severe autosomal dominant nocturnal frontal lobe epilepsy associated with psychiatric disorders and intellectual disability.Semantic proximity Read ↗

A novel KCNT1 mutation in a Chinese family with severe autosomal-dominant nocturnal frontal lobe epilepsySemantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy: an electroclinical study of a Norwegian family with ten affected members.Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy with a mutation in the CHRNB2 gene.Semantic proximity Read ↗

Genetic basis of autosomal dominant nocturnal frontal lobe epilepsy.Semantic proximity Read ↗

Human nocturnal frontal lobe epilepsy: pharmocogenomic profiles of pathogenic nicotinic acetylcholine receptor beta-subunit mutations outside the ion channel pore.Semantic proximity Read ↗

Recent advances on autosomal dominant nocturnal frontal lobe epilepsy: "understanding the nicotinic acetylcholine receptor (nAChR)".Semantic proximity Read ↗

Mutations in familial nocturnal frontal lobe epilepsy might be associated with distinct neurological phenotypes.Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy. A video-polysomnographic and genetic appraisal of 40 patients and delineation of the epileptic syndrome.Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy--a critical overview.Semantic proximity Read ↗

Autosomal dominant nocturnal frontal lobe epilepsy and mild memory impairment associated with CHRNB2 mutation I312M in the neuronal nicotinic acetylcholine receptor.Semantic proximity Read ↗

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