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Journal of Pediatric Endocrinology & Metabolism : JPEM|March 4, 2021
Epileptic phenotype in late-onset hyperinsulinemic hypoglycemia successfully treated by diazoxideJustine Descamps, Cyril Ruello, Kevin Perge, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|June 30, 2020
Early-onset epileptic encephalopathy with migrating focal seizures associated with a FARS2 homozygous nonsense variantDorothée Ville, Gaetan Lesca, Audrey Labalme, et al.
Epilepsy Research|March 15, 2015
Homozygous TBC1D24 mutation in two siblings with familial infantile myoclonic epilepsy (FIME) and moderate intellectual disabilityAnne-Lise Poulat, Dorothée Ville, Julitta de Bellescize, et al.
Epilepsy & Behavior : E&B|January 27, 2022
Sleep disorders and ADHD symptoms in children and adolescents with typical absence seizures: An observational studyMarine Thieux, Maddalena Duca, Benjamin Putois, et al.
Developmental Medicine and Child Neurology|May 7, 2009
Ring 14 chromosome presenting as early-onset isolated partial epilepsyDorothée Ville, Julitta DE Bellescize, Marie Ange Nguyen, et al.
Epilepsy & Behavior : E&B|July 2, 2025
Early age at seizure onset is a risk factor for attention deficit hyperactivity disorder in children with epilepsyIris Caggia, Romain Bouet, Julien Jung, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|November 20, 2023
Antiseizure effect of MEK inhibitor in a child with neurofibromatosis type 1-Developmental and epileptic encephalopathy and optic pathway gliomaSarah Barrière, Cécile Faure-Conter, Pierre Leblond, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|August 7, 2018
Neonatal tremor episodes and hyperekplexia-like presentation at onset in a child with SCN8A developmental and epileptic encephalopathyLinda Pons, Gaëtan Lesca, Damien Sanlaville, et al.
Neuropediatrics|June 22, 2019
Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 MutationVincent Zimmern, Florence Riant, Emmanuel Roze, et al.
Epilepsy Research|March 10, 2009
A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodesJulitta de Bellescize, Nadia Boutry, Elodie Chabrol, et al.
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