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Epilepsia|December 28, 1999
No evidence of a major locus for benign familial infantile convulsions on chromosome 19q12-q13.1E Gennaro, M Malacarne, I Carbone, et al.Brain & Development|April 14, 2009
Early-onset seizure variant of Rett syndrome: definition of the clinical diagnostic criteriaR Artuso, M A Mencarelli, R Polli, et al.Epilepsia|March 1, 1997
Early-onset benign occipital seizure susceptibility syndromeC D Ferrie, A Beaumanoir, R Guerrini, et al.Neurology|July 20, 2007
An open-label trial of levetiracetam in severe myoclonic epilepsy of infancyP Striano, A Coppola, M Pezzella, et al.American Journal of Human Genetics|April 28, 2001
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityM Malacarne, E Gennaro, F Madia, et al.Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.European Journal of Neurology|December 10, 2019
Subgroup comparison according to clinical phenotype and serostatus in autoimmune encephalitis: a multicenter retrospective studyM Gastaldi, S Mariotto, M P Giannoccaro, et al.Epilepsy Research|August 30, 2016
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter studyP De Liso, F Vigevano, N Specchio, et al.Pageof 7