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Brain : a Journal of Neurology|December 20, 2019
Homozygous STXBP1 variant causes encephalopathy and gain-of-function in synaptic transmissionHanna C A Lammertse, Annemiek A van Berkel, Michele Iacomino, et al.Journal of Medical Genetics|May 20, 2022
Gain-of-function p.F28S variant in RAC3 disrupts neuronal differentiation, migration and axonogenesis during cortical development, leading to neurodevelopmental disorderMasashi Nishikawa, Marcello Scala, Muhammad Umair, et al.Expert Opinion on Pharmacotherapy|November 21, 2025
Optimizing pharmacological management of the febrile childMarco Bianchi, Mattia Costa, Fabio Cardinale, et al.Journal of Child Neurology|March 4, 2026
Managing Fever and Vaccination Risks in Dravet Syndrome: From Pathophysiology to Clinical PracticeAlessandro Ferretti, Marco Bianchi, Mattia Costa, et al.Epilepsia|June 15, 2007
Antiepileptic drugs and MTHFR polymorphisms influence hyper-homocysteinemia recurrence in epileptic patientsVincenzo Belcastro, Gorgone Gaetano, Domenico Italiano, et al.Brain & Development|September 19, 2022
Immediate and progressive neurological damage after electrical injury: A pediatric case reportAlfonso Rubino, Pia Bernardo, Carmela Russo, et al.Journal of Child Neurology|October 25, 2011
Electroencephalographic features in dravet syndrome: five-year follow-up study in 22 patientsNicola Specchio, Martina Balestri, Marina Trivisano, et al.Epilepsia|February 15, 2023
Ketamine as advanced second-line treatment in benzodiazepine-refractory convulsive status epilepticus in childrenSilvia Buratti, Emanuele Giacheri, Antonella Palmieri, et al.European Journal of Human Genetics : EJHG|April 3, 2019
Three de novo DDX3X variants associated with distinctive brain developmental abnormalities and brain tumor in intellectually disabled femalesMarcello Scala, Annalaura Torella, Mariasavina Severino, et al.Current Neuropharmacology|March 15, 2017
The α2δ Subunit and Absence Epilepsy: Beyond Calcium Channels?Roberta Celli, Ines Santolini, Michela Guiducci, et al.Pageof 68