1. Early‐onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. Issue 5 (30th September 2012) Authors: Agostinelli, S.; Traverso, M.; Accorsi, P.; Beccaria, F.; Belcastro, V.; Capovilla, G.; Cappanera, S.; Coppola, A.; Dalla Bernardina, B.; Darra, F.; Ferretti, M.; Elia, M.; Galeone, D.; Giordano, L.; Gobbi, G.; Nicita, F.; Parisi, P.; Pezzella, M.; Spalice, A.; Striano, S. Journal: European journal of neurology Issue: Volume 20:Issue 5(2013:May) Page Start: 856 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Pediatric moyamoya disease and syndrome in Italy: Data from the Italian Society of Pediatric Neurology multicentric retrospective study. (June 2017) Authors: Sartori, S.; Po', C.; Carai, A.; Rosati, A.; Accorsi, P.; Iodice, A.; Savasta, S.; D'Avella, D.; Greco, F.; Raviglione, F.; Ragazzi, P.; Agostini, M.; Cesaroni, E.; Di Rosa, G.; Striano, P.; Nicita, F.; Cordelli, D.; Suppiej, A.; Nosadini, M.; Marras, C.E. Journal: European journal of paediatric neurology Issue: Volume 21(2017)Supplement 1 Page Start: e151 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. The natural history of spinal neurofibromatosis: a critical review of clinical and genetic features. (22nd November 2014) Authors: Ruggieri, M.; Polizzi, A.; Spalice, A.; Salpietro, V.; Caltabiano, R.; D'Orazi, V.; Pavone, P.; Pirrone, C.; Magro, G.; Platania, N.; Cavallaro, S.; Muglia, M.; Nicita, F. Journal: Clinical genetics Issue: Volume 87:Number 5(2015:May) Page Start: 401 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗