Pierre Szepetowski

Marseille, France

Last Updated: 09/26/2026

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Found 27 publications

Spontaneous spike-and-wave discharges during sleep in mice: circadian distribution and impact on sleep quality.

Spontaneous spike-and-wave discharges during sleep in mice: circadian distribution and impact on sleep quality.

Journal: Frontiers in neurology

Published: August 28, 2025

Genetic epilepsy: which tests, for whom, why?

Genetic epilepsy: which tests, for whom, why?

Journal: La Revue du praticien

Published: December 03, 2024

Cytomegalovirus infection of the fetal brain: intake of aspirin during pregnancy blunts neurodevelopmental pathogenesis in the offspring.

Cytomegalovirus infection of the fetal brain: intake of aspirin during pregnancy blunts neurodevelopmental pathogenesis in the offspring.

Journal: Journal of neuroinflammation

Published: May 13, 2024

Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C N-methyl-D-aspartate receptors.

Pathogenic MTOR somatic variant causing focal cortical dysplasia drives hyperexcitability via overactivation of neuronal GluN2C N-methyl-D-aspartate receptors.

Journal: Epilepsia

Published: January 25, 2024

New insights into the genetics of stuttering.

New insights into the genetics of stuttering.

Journal: Brain : a journal of neurology

Published: October 24, 2023

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.

Neurodevelopmental and Epilepsy Phenotypes in Individuals With Missense Variants in the Voltage-Sensing and Pore Domains of KCNH5.

Journal: Neurology

Published: April 28, 2022

The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel.

The Epilepsy of Infancy With Migrating Focal Seizures: Identification of de novo Mutations of the KCNT2 Gene That Exert Inhibitory Effects on the Corresponding Heteromeric KNa1.1/KNa1.2 Potassium Channel.

Journal: Frontiers in cellular neuroscience

Published: July 11, 2019

Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations.

Update on the genetics of the epilepsy-aphasia spectrum and role of GRIN2A mutations.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: June 01, 2019

Impaired vocal communication, sleep-related discharges, and transient alteration of slow-wave sleep in developing mice lacking the GluN2A subunit of N-methyl-d-aspartate receptors.

Impaired vocal communication, sleep-related discharges, and transient alteration of slow-wave sleep in developing mice lacking the GluN2A subunit of N-methyl-d-aspartate receptors.

Journal: Epilepsia

Published: January 11, 2019

In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal Brain.

In Utero Administration of Drugs Targeting Microglia Improves the Neurodevelopmental Outcome Following Cytomegalovirus Infection of the Rat Fetal Brain.

Journal: Frontiers in cellular neuroscience

Published: November 29, 2017

Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host Cells.

Magnetofection™ of NMDA Receptor Subunits GluN1 and GluN2A Expression Vectors in Non-Neuronal Host Cells.

Journal: Methods in molecular biology (Clifton, N.J.)

Published: October 08, 2017

Genetics of human epilepsies: Continuing progress.

Genetics of human epilepsies: Continuing progress.

Journal: Presse medicale (Paris, France : 1983)

Published: September 29, 2017

Showing 1-12 of 27

Last Updated: 09/26/2026