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 further contribution to the delineation of epileptic phenotype in PACS2-related syndrome.

Seizure - 1 Jul 2020

Terrone Gaetano, Marchese Francesca, Vari Maria Stella, Severino Mariasavina, Madia Francesca, Amadori Elisabetta, Del Giudice Ennio, Romano Alfonso, Gennaro Elena, Zara Federico, Striano Pasquale

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Brain
Share to Epilepsy
Share to Infant, Newborn
Share to Magnetic Resonance Imaging

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenobarbital

Share to Phenotype

Share to Sodium Channel Blockers

Share to Vesicular Transport Proteins

Source

Identifiers

PMID: 32416568
DOI: 10.1016/j.seizure.2020.05.001

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A further contribution to the delineation of epileptic phenotype in PACS2-related syndrome.PMID 32416568Read ↗

Clinical variations of epileptic syndrome associated with PACS2 variant.Semantic proximity Read ↗

First reported case of an inherited PACS2 pathogenic variant with variable expressionSemantic proximity Read ↗

Epileptic Encephalopathies: New Genes and New PathwaysSemantic proximity Read ↗

Characteristics of Developmental and Epileptic Encephalopathy Associated with PACS2 p.Glu209Lys Pathogenic Variant-Our Experience and Systematic Review of the Literature.Semantic proximity Read ↗

Dravet syndrome: inroads into understanding epileptic encephalopathies.Semantic proximity Read ↗

PACS gene family-related neurological diseases: limited genotypes and diverse phenotypes.Semantic proximity Read ↗

PACS2 pathogenic variant associated with malformation of cortical development and epilepsy.Semantic proximity Read ↗

PIGA-related epileptic encephalopathy demonstrating intrafamilial phenotypic heterogeneity.Semantic proximity Read ↗

Epileptic seizures as a presentation of central nervous system involvement in TTR Val30Met-FAP.Semantic proximity Read ↗

KCNQ2 Epileptic Encephalopathy in Early Infancy.Semantic proximity Read ↗

Generalized epileptic disorders: an update.Semantic proximity Read ↗

Epileptic encephalopathy patients with SCN2A variant initiated by neonatal seizure.Semantic proximity Read ↗

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