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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 7, 2025
Fulfilling the needs of caregivers in delivering health services to children with developmental and epileptic encephalopathiesLauren Kelada, Stephanie Best, Kristine Pierce, et al.
Epilepsia|May 5, 2026
Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoidsCristiana Mattei, Miaomiao Mao, Sean Byars, et al.
Epilepsia Open|May 25, 2021
Seizures in Sotos syndrome: Phenotyping in 49 patientsOlivier Fortin, Christian Vincelette, Afsheen Q Khan, et al.
Translational Psychiatry|January 27, 2024
Multiomic analysis implicates nuclear hormone receptor signalling in clustering epilepsyRebekah de Nys, Clare L van Eyk, Tarin Ritchie, et al.
Epilepsia|May 24, 2025
Serial correlation between saliva and blood beta-hydroxybutyrate levels in children commencing the ketogenic diet for epilepsyNeha Kaul, Jing Duan, Dong Cui, et al.
Pediatrics|August 24, 2019
Fragile Females: Case Series of Epilepsy in Girls With FMR1 DisruptionKenneth A Myers, Femke N G van 't Hof, Lynette G Sadleir, et al.
Epilepsy Research|January 26, 2018
Childhood-onset generalized epilepsy in Bainbridge-Ropers syndromeKenneth A Myers, Susan M White, Shehla Mohammed, et al.
Epilepsia|June 7, 2024
SCN8A self-limited infantile epilepsy: Does epilepsy resolve?Emma Young, Rebekah Harris, Nico Lieffering, et al.
Epilepsia|November 5, 2011
Clinical and neurophysiologic features of progressive myoclonus epilepsy without renal failure caused by SCARB2 mutationsGuido Rubboli, Silvana Franceschetti, Samuel F Berkovic, et al.
Epilepsia|February 22, 2023
IRF2BPL: A new genotype for progressive myoclonus epilepsiesCinzia Costa, Karen L Oliver, Carmen Calvello, et al.
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