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Journal of Medical Genetics|October 6, 2018
PEHO syndrome: the endpoint of different genetic epilepsiesManali Chitre, Michael S Nahorski, Kaitlin Stouffer, et al.Frontiers in Neurology|April 1, 2022
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical ApplicationsGiorgio Costagliola, Greta Depietri, Alexandre Michev, et al.American Journal of Medical Genetics. Part A|April 15, 2008
No major role for the EMX2 gene in schizencephalyElisa Merello, Eric Swanson, Patrizia De Marco, et al.Seizure|November 5, 2018
The pharmacological management of Lennox-Gastaut syndrome and critical literature reviewAlberto Verrotti, Pasquale Striano, Giulia Iapadre, et al.Epilepsy & Behavior : E&B|February 26, 2022
De novo GRIN2A variants associated with epilepsy and autism and literature reviewGiuseppe Donato Mangano, Antonella Riva, Antonina Fontana, et al.Frontiers in Neurology|May 18, 2026
Is cognitive profiling in NF1 still optional? A systematic review of current assessment practicesAndrea Santangelo, Alessandra Sardi, Luca Bergonzini, et al.Journal of Clinical Medicine|July 29, 2025
Post-COVID Surge in Pediatric Emergency Department Accesses for Psychiatric Conditions: A Retrospective Analysis of Anxiety, Self-Injury Behaviors, and Psychomotor AgitationTommaso Bellini, Silvia Merlo, Andrea Lacovara, et al.Frontiers in Pediatrics|March 16, 2023
Case report: Revascularization failure in NF1-related moyamoya syndrome after selumetinib: A possible pathophysiological correlation?Cristina Chelleri, Marcello Scala, Patrizia De Marco, et al.European Journal of Medical Genetics|November 5, 2022
Hydranencephaly in CENPJ-related Seckel syndromeClaudia Cuccurullo, Giuseppina Miele, Gianluca Piccolo, et al.Epilepsia Open|July 3, 2026
Expanding the electroclinical spectrum of TANC2-related disorders: Lennox-Gastaut syndrome and related developmental epileptic phenotypesLorenzo Perilli, Carlotta Stipa, Gianmichele Villano, et al.Pageof 77