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Italian Journal of Pediatrics|January 13, 2022
Eligibility criteria for pediatric patients who may benefit from anti SARS-CoV-2 monoclonal antibody therapy administration: an Italian inter-society consensus statementMarcello Lanari, Elisabetta Venturini, Luca Pierantoni, et al.Epilepsy Research|July 24, 2012
Reflex myoclonic epilepsy in infancy: a multicenter clinical studyAlberto Verrotti, Sara Matricardi, Giuseppe Capovilla, et al.The Journal of Pediatrics|September 3, 2013
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with Down syndromeAlberto Verrotti, Raffaella Cusmai, Francesco Nicita, et al.Developmental Medicine and Child Neurology|July 27, 2010
Intracerebral large artery disease in Aicardi-Goutières syndrome implicates SAMHD1 in vascular homeostasisVenkateswaran Ramesh, Bruno Bernardi, Altin Stafa, et al.Annals of Neurology|February 26, 2005
Unusual variants of Alexander's diseaseMarjo S van der Knaap, Gajja S Salomons, Rong Li, et al.BMC Psychiatry|February 1, 2012
The characteristics and activities of child and adolescent mental health services in Italy: a regional surveyLaura Pedrini, Giovanni Colasurdo, Stefano Costa, et al.Epilepsy Research|December 15, 2010
Benign convulsions associated with mild gastroenteritis: a multicenter clinical studyAlberto Verrotti, Giuliana Nanni, Sergio Agostinelli, et al.Human Molecular Genetics|February 22, 2014
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotypePamela Magini, Tommaso Pippucci, I-Chun Tsai, et al.Human Mutation|January 30, 2009
Mutations in MFSD8/CLN7 are a frequent cause of variant-late infantile neuronal ceroid lipofuscinosisChiara Aiello, Alessandra Terracciano, Alessandro Simonati, et al.Journal of Neurology|October 19, 2014
Long-term outcome of epilepsy in patients with Prader-Willi syndromeAlberto Verrotti, Raffaella Cusmai, Daniela Laino, et al.Pageof 7