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 Dysfunction in Juvenile Myoclonic Epilepsy (JME) – A Tertiary Care Center Study

6 May 2020

Abstract excerpt

BACKGROUND AND AIM: Epilepsy often leads to cognitive impairment. Idiopathic generalized epilepsy as a group is considered to be benign in terms of its effects on cognition. Though, neuropsychological testing reveals subtle frontal impairment in patients with juvenile myoclonic epilepsy (JME). The aim of this study is to evaluate cognitive dysfunction in patients with JME. METHOD: We compared 50 JME patients and...

Read the complete abstract on PubMed

Topics

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

Share to Epilepsy research and treatment
Share to Genetics and Neurodevelopmental Disorders
Share to Glycogen Storage Diseases and Myoclonus

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 33911378
DOI: 10.4103/aian.aian_663_19

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cognitive Dysfunction in Juvenile Myoclonic Epilepsy (JME) – A Tertiary Care Center StudyPMID 33911378Read ↗

Cognitive phenotype of juvenile absence epilepsy: An investigation of patients and unaffected siblings.Semantic proximity Read ↗

The cognitive phenotype of juvenile absence epilepsy and its heritability: An investigation of patients and unaffected siblingsSemantic proximity Read ↗

Delineating behavioral and cognitive phenotypes in juvenile myoclonic epilepsy: Are we missing the forest for the trees?Semantic proximity Read ↗

Latent cognitive phenotypes in juvenile myoclonic epilepsy: Clinical, sociodemographic, and neuroimaging associations.Semantic proximity Read ↗

Prospective memory in patients with juvenile myoclonic epilepsy and their healthy siblings.Semantic proximity Read ↗

Cognitive phenotypes in frontal lobe epilepsy.Semantic proximity Read ↗

Cognitive phenotypes in childhood idiopathic epilepsies.Semantic proximity Read ↗

Mechanisms, genetics, and pathogenesis of juvenile myoclonic epilepsy: reviewSemantic proximity Read ↗

Familial association of neuropsychological traits in patients with generalized and partial seizure disorders.Semantic proximity Read ↗

Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients.Semantic proximity Read ↗

Andersen-Tawil syndrome: definition of a neurocognitive phenotype.Semantic proximity Read ↗

Cognitive phenotypes in adults with temporal lobe epilepsy from South Africa - A contribution to the international classification of cognitive disorders in epilepsy (IC-CoDE).Semantic proximity Read ↗

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