Mutations in the IRBIT domain of ITPR1 are a frequent cause of autosomal dominant nonprogressive congenital ataxia von Barresi, S., Niceta, M., Alfieri, P., Brankovic, V., Piccini, G., Bruselles, A., Barone, M.R., Cusmai, R., Tartaglia, M., Bertini, E., Zanni, G.

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Neuroimaging Changes in Menkes Disease, Part 1 von Manara, R, D'Agata, L, Rocco, M C, Cusmai, R, Freri, E, Pinelli, L, Darra, F, Procopio, E, Mardari, R, Zanus, C, Di Rosa, G, Soddu, C, Severino, M, Ermani, M, Longo, D, Sartori, S

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Effectiveness and tolerability of Perampanel in children and adolescents with refractory epilepsies − an Italian observational multicenter study von De Liso, P, Vigevano, F, Specchio, N, De Palma, L, Bonanni, P, Osanni, E, Coppola, G, Parisi, P, Grosso, S, Verrotti, A, Spalice, A, Nicita, F, Zamponi, N, Siliquini, S, Giordano, L, Martelli, P, Guerrini, R, Rosati, A, Ilvento, L, Belcastro, V, Striano, P, Vari, M.S, Capovilla, G, Beccari, F, Bruni, O, Luchetti, A, Gobbi, G, Russo, A, Pruna, D, Tozzi, A.E, Cusmai, R

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Neuroimaging Changes in Menkes Disease, Part 2 von Manara, R, Rocco, M C, D'agata, L, Cusmai, R, Freri, E, Giordano, L, Darra, F, Procopio, E, Toldo, I, Peruzzi, C, Vittorini, R, Spalice, A, Fusco, C, Nosadini, M, Longo, D, Sartori, S

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Electroclinical findings and long‐term outcomes in epileptic patients with inv dup (15) von Matricardi, S., Darra, F., Spalice, A., Basti, C., Fontana, E., Dalla Bernardina, B., Elia, M., Giordano, L., Accorsi, P., Cusmai, R., De Liso, P., Romeo, A., Ragona, F., Granata, T., Concolino, D., Carotenuto, M., Pavone, P., Pruna, D., Striano, P., Savasta, S., Verrotti, A.

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De novo Absence Status Epilepticus in a pediatric cohort: Electroclinical pattern in a multicenter Italian patients cohort von Pepi, C., Cesaroni, E., Striano, P., Maiorani, D., Pruna, D., Cossu, S., Di Capua, M., Vigevano, F., Specchio, N., Cusmai, R.

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Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome von Grosso, S., Coppola, G., Cusmai, R., Parisi, P., Spalice, A., Foligno, S., Verrotti, A., Balestri, P.

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Clinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication von Verrotti, A., Laino, D., Rinaldi, V. E., Suppiej, A., Giordano, L., Toldo, I., Margari, L., Parisi, P., Rizzo, R., Matricardi, S., Cusmai, R., Grosso, S., Gaggero, R., Zamponi, N., Pavone, P., Capovilla, G., Rauchenzauner, M., Cerminara, C., Di Gennaro, G., Esposito, M., Striano, P., Savasta, S., Coppola, G., Siliquini, S., Operto, F., Belcastro, V., Ragona, F., Marseglia, G. L., Spalice, A.

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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH) von des Portes, Vincent, Francis, Fiona, Pinard, Jean-Marc, Desguerre, Isabelle, Moutard, Marie-Laure, Snoeck, Irina, Meiners, Linda C., Capron, François, Cusmai, Raffaella, Ricci, Stefano, Motte, Jacques, Echenne, Bernard, Ponsot, Gérard, Dulac, Olivier, Chelly, Jamel, Beldjord, Cherif

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Childhood refractory focal epilepsy following acute febrile encephalopathy von Specchio, N., Fusco, L., Claps, D., Trivisano, M., Longo, D., Cilio, M. R., Valeriani, M., Cusmai, R., Cappelletti, S., Gentile, S., Fariello, G., Specchio, L. M., Vigevano, F.

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Neuroimaging Changes in Menkes Disease, Part 1 von Manara, R., D'Agata, L., Rocco, M.C., Cusmai, R., Freri, E., Pinelli, L., Darra, F., Procopio, E., Mardari, R., Zanus, C., Di Rosa, G., Soddu, C., Severino, M., Ermani, M., Longo, D., Sartori, S.

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Infantile ascending hereditary spastic paralysis (IAHSP): Clinical features in 11 families von LESCA, G, EYMARD-PIERRE, E, BOESPFLUG-TANGUY, O, BERTINI, E, SANTORELLI, F. M, CUSMAI, R, DI CAPUA, M, VALENTE, E. M, ATTIA-SOBOL, J, PLAUCHU, H, LEUZZI, V, PONZONE, A

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Mucositis pain: treatment pptions for the patient von Antonacci, G., Cerati, C., Racis, M., Lo Russo, I., Togliardi, E., Cusmai, R., Saibene, G.

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Neuropsychiatric Aspects of Tuberous Sclerosis von CURATOLO, P., CUSMAI, R., CORTESI, F., CHIRON, C., JAMBAQUE, I., DULAC, O.

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Convulsions associated with gastroenteritis in the spectrum of benign focal epilepsies in infancy: 30 cases including four cases with ictal EEG recording von Cusmai, Raffaella, Jocic-Jakubi, Bosanka, Cantonetti, Laura, Japaridze, Natia, Vigevano, Federico

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PP6.2 – 1668 Early EEG monitoring following prenatal diagnosis predicts epileptogenesis in tuberous sclerosis von Moavero, R, Cusmai, R, Vigevano, F, Toscano, A, Caforio, L, Bernardi, B

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PS-033 Ifosfamide induced encephalopathy: prophylaxis and therapy with methylene blue von Gambitta, L, Togliardi, E, Cusmai, R, Costanza, C Della, Nurro, S, Ruffino, E, Saibene, G

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P01.1 Epilepsy and cognitive long-term outcome is improved by prompt seizure control in children with tuberous sclerosis von Cusmai, R., Moavero, R., Bombardieri, R., Vigevano, F., Curatolo, P.

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The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience von Coppola, Giangennaro, Veggiotti, Pierangelo, Cusmai, Raffaella, Bertoli, Simona, Cardinali, Simonetta, Dionisi-Vici, Carlo, Elia, Mirella, Lispi, Maria Luisa, Sarnelli, Chiara, Tagliabue, Anna, Toraldo, Caterina, Pascotto, Antonio

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P280 – 1775 Neurophysiological features in congenital disorders of glycosylation von Cusmai, R, Pro, S, Balestri, M, Moavero, R, Dionisi Vici, C, Bevivino, E, Vigevano, F, Martinelli, D

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