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

Clinical genetic study in juvenile myoclonic epilepsy.

Seizure - 1 Nov 2014

Cvetkovska Emilija, Panov Sasho, Kuzmanovski Igor

Abstract excerpt

PURPOSE: To evaluate clinical features of probands with juvenile myoclonic epilepsy (JME) and affected members of their families in order to study clinical genetics of JME. METHOD: Thirteen unrelated families with at least two members with history of seizures were identified; clinical and genealogic data were collected from JME probands and family members. RESULTS: All probands had myoclonic and generalized...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Child
Share to Electroencephalography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Family

Share to Genetic Testing

Share to Myoclonic Epilepsy, Juvenile

Share to Pedigree

Share to Young Adult

Source

Identifiers

PMID: 25108570
DOI: 10.1016/j.seizure.2014.07.011

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical genetic study in juvenile myoclonic epilepsy.PMID 25108570Read ↗

Phenotypic analysis of juvenile myoclonic epilepsy in Indian families.Semantic proximity Read ↗

Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.Semantic proximity Read ↗

Clinical characteristics of a South Indian cohort of juvenile myoclonic epilepsy probands.Semantic proximity Read ↗

Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.Semantic proximity Read ↗

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

Juvenile myoclonic epilepsy as a spectrum disorder: A focused review.Semantic proximity Read ↗

Occurrence of only myoclonic jerks in juvenile myoclonic epilepsy.Semantic proximity Read ↗

[Genetic aspects of juvenile myoclonic epilepsy].Semantic proximity Read ↗

Clinical and electroencephalographic study of first-degree relatives and probands with juvenile myoclonic epilepsySemantic proximity Read ↗

Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy.Semantic proximity Read ↗

Variation in prognosis and treatment outcome in juvenile myoclonic epilepsy: a Biology of Juvenile Myoclonic Epilepsy Consortium proposal for a practical definition and stratified medicine classificationsSemantic proximity Read ↗

Predictive value of EFHC1 variants for the long-term seizure outcome in juvenile myoclonic epilepsy.Semantic proximity Read ↗

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