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

Cognitive and functional status in late-onset Lennox-Gastaut syndrome: Variation on a classic phenotype.

Epilepsy & behavior : E&B - 1 Jan 2020

Chourasia Nitish, Maheshwari Atul, Kalamangalam Giridhar

Abstract excerpt

Lennox-Gastaut syndrome (LGS) denotes a refractory epileptic encephalopathy of childhood onset with the triad of generalized slow spike-wave (GSSW) on interictal scalp electroencephalogram (EEG), multiple seizure types, and intellectual impairment. The neurobiology of LGS is said to sustain abnormal patterns of brain activity and connectivity that ultimately impair normal cerebral developmental mechanisms....

Read the complete abstract on PubMed

Topics

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

Share to Activities of Daily Living
Share to Age of Onset
Share to Brain

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to Cognition

Share to Cohort Studies

Share to Electroencephalography

Share to Magnetic Resonance Imaging

Source

Identifiers

PMID: 31770718
DOI: 10.1016/j.yebeh.2019.106660

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

Cognitive and functional status in late-onset Lennox-Gastaut syndrome: Variation on a classic phenotype.PMID 31770718Read ↗

Lennox-Gastaut syndrome of unknown cause: phenotypic characteristics of patients in the Epilepsy Phenome/Genome Project.Semantic proximity Read ↗

An atypical case of Lennox-Gastaut syndrome not associated with mental retardation: a nosological issue.Semantic proximity Read ↗

Asymmetric Slow-Spike-Wave Patterns with Maximal Discharges Contralateral to MRI Lesions Predict Better Surgical Prognosis in Symptomatic Lennox-Gastaut Syndrome or Lennox-Gastaut Phenotypes.Semantic proximity Read ↗

Epilepsy in Aicardi-Goutières syndrome.Semantic proximity Read ↗

Lennox-Gastaut syndrome and phenotype: secondary network epilepsies.Semantic proximity Read ↗

Expanding the clinical and EEG spectrum of CNKSR2-related encephalopathy with status epilepticus during slow sleep (ESES).Semantic proximity Read ↗

Polymicrogyria-associated epilepsy: a multicenter phenotypic study from the Epilepsy Phenome/Genome Project.Semantic proximity Read ↗

A Multicenter Retrospective Observational Cohort Study of Seizure Freedom before Lennox-Gastaut Syndrome (the “Gap”). Opportunities for PreventionSemantic proximity Read ↗

GRIN2A mutations in acquired epileptic aphasia and related childhood focal epilepsies and encephalopathies with speech and language dysfunction.Semantic proximity Read ↗

Pediatric focal epilepsy syndromes.Semantic proximity Read ↗

EEG abnormalities in patients with chronic neuronopathic Gaucher disease: A retrospective review.Semantic proximity Read ↗

Long-term characterization of cognitive phenotypes in children with seizures over 36 months.Semantic proximity Read ↗

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