Nathalie Villeneuve

Marseille, France

Last Updated: 09/26/2026

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Found 70 publications

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

Journal: Neurology
Published: May 26, 2026

Prolonged fenfluramine use in open-label studies of Dravet or Lennox-Gastaut syndromes: Long-term safety, tolerability, patient global functioning, and considerations for interpreting effectiveness.

Prolonged fenfluramine use in open-label studies of Dravet or Lennox-Gastaut syndromes: Long-term safety, tolerability, patient global functioning, and considerations for interpreting effectiveness.

Journal: Epilepsia
Published: March 13, 2026

Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy.

Compound heterozygous SLC12A5 variants expand the molecular and functional spectrum of KCC2-developmental and epileptic encephalopathy.

Journal: Epilepsia
Published: November 13, 2025

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Early sodium channel blocker initiation is associated with better outcomes in KCNQ2 disorders.

Journal: Brain : a journal of neurology
Published: October 17, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Journal: medRxiv : the preprint server for health sciences
Published: September 15, 2025

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Journal: Nature genetics
Published: September 02, 2025

Long-term outcomes of a cohort of patients with pharmacoresistant neonatal epilepsy and negative brain MRI.

Long-term outcomes of a cohort of patients with pharmacoresistant neonatal epilepsy and negative brain MRI.

Journal: Epilepsia open
Published: April 22, 2025

The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis.

The Clinical and Genetic Landscape of a French Multicenter Cohort of 2563 Epilepsy Patients Referred for Genetic Diagnosis.

Journal: European journal of neurology
Published: April 22, 2025

GABRA2-related encephalopathy: Identification of two phenotypes with distinctive electroclinical features.

GABRA2-related encephalopathy: Identification of two phenotypes with distinctive electroclinical features.

Journal: Epilepsia
Published: January 20, 2025

Anomia prehabilitation in temporal lobe epilepsy surgery: A pilot study.

Anomia prehabilitation in temporal lobe epilepsy surgery: A pilot study.

Journal: Epilepsia
Published: October 03, 2024

KCNMA1-Related Episodes of Behavioral Arrest and Loss of Postural Reflexes: A Critical Reappraisal.

KCNMA1-Related Episodes of Behavioral Arrest and Loss of Postural Reflexes: A Critical Reappraisal.

Journal: Movement disorders clinical practice
Published: July 19, 2024

Stereoelectroencephalographic exploration and surgical outcome in Lennox-Gastaut syndrome.

Stereoelectroencephalographic exploration and surgical outcome in Lennox-Gastaut syndrome.

Journal: Epilepsia
Published: July 17, 2024
Showing 1-12 of 70

Last Updated: 09/26/2026