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Epilepsy & Behavior : E&B|May 16, 2016
Autism spectrum disorder phenotype and intellectual disability in females with epilepsy and PCDH-19 mutationsDelphine Breuillard, Dorothée Leunen, Nicole Chemaly, et al.
European Journal of Neurology|September 19, 2025
Assessing Real World Efficacy, Safety, and 18-Month Retention Rates of Cannabidiol in Individuals With Drug Resistant EpilepsiesNicole Chemaly, Mathieu Kuchenbuch, Emma Losito, et al.
Developmental Medicine and Child Neurology|August 9, 2013
Hemiconvulsion-hemiplegia syndrome revisited: longitudinal MRI findings in 10 childrenGiulia Barcia, Isabelle Desguerre, Orietta Carmona, et al.
Epilepsy Research|July 9, 2016
Patients with dravet syndrome in the era of stiripentol: A French cohort cross-sectional studyPaola De Liso, Nicole Chemaly, Jacques Laschet, et al.
Epilepsia|November 11, 2024
Transition from pediatric to adult care system in patients with complex epilepsies: Necker model for transition evaluated on 70 consecutive patientsRima Nabbout, Agathe Molimard, Giovanna Scorrano, et al.
European Journal of Medical Genetics|October 18, 2024
Exploring the clinical spectrum of CNTNAP2-related neurodevelopmental disorders: A case series and a literature appraisalGiulia Barcia, Giovanna Scorrano, Marlène Rio, et al.
Orphanet Journal of Rare Diseases|November 15, 2013
Encephalopathy in children with Dravet syndrome is not a pure consequence of epilepsyRima Nabbout, Nicole Chemaly, Mathilde Chipaux, et al.
Epilepsia Open|November 8, 2021
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and familiesNicole Chemaly, Mathieu Kuchenbuch, Théo Teng, et al.
Developmental Medicine and Child Neurology|November 12, 2025
Intravenous immunoglobulin and febrile status epilepticus in children with Dravet syndrome: A retrospective multicentre studyRomane Marc, Nicole Chemaly, Mathieu Kuchenbuch, et al.
Epilepsia Open|March 15, 2019
Autism spectrum disorder and cognitive profile in children with Dravet syndrome: Delineation of a specific phenotypeLisa Ouss, Dorothee Leunen, Jacques Laschet, et al.
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