Julitta De Bellescize

Lyon, France

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 45 publications

Ictal semiology in fronto-opercular epilepsy: A systematic review.

Ictal semiology in fronto-opercular epilepsy: A systematic review.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: October 17, 2025

Interictal epileptiform discharges are involved in momentary lapses of attention in children with epilepsy.

Interictal epileptiform discharges are involved in momentary lapses of attention in children with epilepsy.

Journal: Epilepsia

Published: July 15, 2025

Early age at seizure onset is a risk factor for attention deficit hyperactivity disorder in children with epilepsy.

Early age at seizure onset is a risk factor for attention deficit hyperactivity disorder in children with epilepsy.

Journal: Epilepsy & behavior : E&B

Published: March 21, 2025

RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures.

RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: June 28, 2024

Molecular and Phenotypic Characterization of the RORB-Related Disorder.

Molecular and Phenotypic Characterization of the RORB-Related Disorder.

Journal: Neurology

Published: January 02, 2024

Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy.

Expanding the Mutational Landscape and Clinical Phenotype of CHD2-Related Encephalopathy.

Journal: Neurology. Genetics

Published: December 07, 2023

Antiseizure effect of MEK inhibitor in a child with neurofibromatosis type 1-Developmental and epileptic encephalopathy and optic pathway glioma.

Antiseizure effect of MEK inhibitor in a child with neurofibromatosis type 1-Developmental and epileptic encephalopathy and optic pathway glioma.

Journal: Epileptic disorders : international epilepsy journal with videotape

Published: July 23, 2023

KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.

KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism.

Journal: EBioMedicine

Published: January 22, 2022

Sleep disorders and ADHD symptoms in children and adolescents with typical absence seizures: An observational study.

Sleep disorders and ADHD symptoms in children and adolescents with typical absence seizures: An observational study.

Journal: Epilepsy & behavior : E&B

Published: August 23, 2021

STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes.

STAG2 microduplication in a patient with eyelid myoclonia and absences and a review of EMA-related reported genes.

Journal: European journal of medical genetics

Published: May 16, 2021

The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies.

The EPIGENE network: A French initiative to harmonize and improve the nationwide diagnosis of monogenic epilepsies.

Journal: European journal of medical genetics

Published: May 05, 2021

Epileptic phenotype in late-onset hyperinsulinemic hypoglycemia successfully treated by diazoxide.

Epileptic phenotype in late-onset hyperinsulinemic hypoglycemia successfully treated by diazoxide.

Journal: Journal of pediatric endocrinology & metabolism : JPEM

Published: July 03, 2020

Showing 1-12 of 45

Last Updated: 09/26/2026