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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 4, 2026
In search of "what really matters": Insights from a web-based survey on Patient-Centered Outcomes in GLUT1DSCostanza Varesio, Ludovica Pasca, Martina Paola Zanaboni, et al.Journal of Neurology|March 3, 2005
Autosomal recessive progressive myoclonus epilepsy with ataxia and mental retardationGiovanni Coppola, Chiara Criscuolo, Giuseppe De Michele, et al.Epilepsy Research|January 25, 2015
Autosomal dominant lateral temporal epilepsy (ADLTE): novel structural and single-nucleotide LGI1 mutations in families with predominant visual aurasEmanuela Dazzo, Lia Santulli, Annio Posar, et al.Veterinary Journal (London, England : 1997)|February 15, 2023
Translational veterinary epilepsy: A win-win situation for human and veterinary neurologyMarios Charalambous, Andrea Fischer, Heidrun Potschka, et al.Epilepsia|March 10, 2017
Instruction manual for the ILAE 2017 operational classification of seizure typesRobert S Fisher, J Helen Cross, Carol D'Souza, et al.Epilepsia|May 3, 2022
ILAE classification and definition of epilepsy syndromes with onset in neonates and infants: Position statement by the ILAE Task Force on Nosology and DefinitionsSameer M Zuberi, Elaine Wirrell, Elissa Yozawitz, et al.Epilepsia|October 5, 2022
Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension studyKelly G Knupp, Ingrid E Scheffer, Berten Ceulemans, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|April 12, 2026
Transition from paediatric to adult care in paediatric-onset neurological disorders in Europe: A survey and scoping reviewDana Craiu, Maria T Papadopoulou, Jasna Orazem Mrak, et al.European Journal of Neurology|September 14, 2021
Epilepsy, electroclinical features, and long-term outcomes in Pitt-Hopkins syndrome due to pathogenic variants in the TCF4 geneSara Matricardi, Paolo Bonanni, Giulia Iapadre, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|August 14, 2016
Epilepsy in the setting of full trisomy 18: A multicenter study on 18 affected children with and without structural brain abnormalitiesSara Matricardi, Alberto Spalice, Vincenzo Salpietro, et al.Pageof 77