The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion von Baroncelli, G. I., Carlucci, G., Freri, E., Giuca, M. R., Guarnieri, V., Navarra, G., Toschi, B., Mora, S.

Volltext

Correction to: The diagnosis of hypophosphatasia in children as a multidisciplinary effort: an expert opinion von Baroncelli, G. I., Carlucci, G., Freri, E., Giuca, M. R., Guarnieri, V., Navarra, G., Toschi, B., Mora, S.

Volltext

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

Volltext

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

Volltext

2. Follow-up of five cases with Rasmussen encephalitis with magnetoencephalography von Rossi, D.S, Visani, E, Duran, D, Rotondi, F, Canafoglia, L, Freri, E, Ragona, F, Granata, T, Panzica, F, Franceschetti, S

Volltext

Experience with immunomodulatory treatments in Rasmussen's encephalitis von GRANATA, T, FUSCO, L, VIGEVANO, F, DALLA BERNARDINA, B, SPREAFICO, R, ANTOZZI, C, GOBBI, G, FRERI, E, RAGONA, F, BROGGI, G, MANTEGAZZA, R, GIORDANO, L, VILLANI, F, CAPOVILLA, G

Volltext

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.

Volltext

Rasmussen's encephalitis: Early characteristics allow diagnosis von GRANATA, T, GOBBI, G, BERTANI, G, CASAZZA, M, DALLA BERNARDINA, B, FUSCO, L, SPREAFICO, R, VIGEVANO, F, CAPOVILLA, G, RAGONA, F, FRERI, E, CHIAPPARINI, L, BERNASCONI, P, GIORDANO, L

Volltext

Diagnostic imaging in 13 cases of Rasmussen's encephalitis: Can early MRI suggest the diagnosis? von CHIAPPARINI, L, GRANATA, T, TASSI, L, GIORDANO, L, VIRI, M, DALLA BERNARDINA, B, SPREAFICO, R, SAVOIARDO, M, FARINA, L, CICERI, E, ERBETTA, A, RAGONA, F, FRERI, E, FUSCO, L, GOBBI, G, CAPOVILLA, G

Volltext

Early clinical and EEG findings associated with the outcome in childhood absence epilepsy von Canafoglia, Laura, Dettori, Maria Sabina, Duran, Dunja, Ragona, Francesca, Freri, Elena, Casellato, Susanna, Granata, Tiziana, Franceschetti, Silvana, Panzica, Ferruccio

Volltext

Anakinra usage in febrile infection related epilepsy syndrome: an international cohort von Lai, Yi‐Chen, Muscal, Eyal, Wells, Elizabeth, Shukla, Nikita, Eschbach, Krista, Hyeong Lee, Ki, Kaliakatsos, Marios, Desai, Nevedita, Wickström, Ronny, Viri, Maurizio, Freri, Elena, Granata, Tiziana, Nangia, Srishti, Dilena, Robertino, Brunklaus, Andreas, Wainwright, Mark S., Gorman, Mark P., Stredny, Coral M., Asiri, Abdurhman, Hundallah, Khalid, Doja, Asif, Payne, Eric, Wirrell, Elaine, Koh, Sookyong, Carpenter, Jessica L., Riviello, James

Volltext

De novo monoallelic Reelin missense variants cause dominant neuronal migration disorders via a dominant-negative mechanism von Riva, Martina, Ferreira, Sofia, Hayashi, Kotaro, Saillour, Yoann, Medvedeva, Vera P, Honda, Takao, Hayashi, Kanehiro, Altersitz, Claire, Albadri, Shahad, Rosello, Marion, Dang, Julie, Serafini, Malo, Causeret, Frédéric, Henry, Olivia J, Roux, Charles-Joris, Bellesme, Céline, Freri, Elena, Josifova, Dragana, Parrini, Elena, Guerrini, Renzo, Del Bene, Filippo, Nakajima, Kazunori, Bahi-Buisson, Nadia, Pierani, Alessandra

Volltext

P20.02.B ELECTRO-CLINICAL, NEUROIMAGING FEATURES AND NEUROPATHOLOGICAL CHARACTERIZATION OF POLYMORPHOUS LOW-GRADE NEUROEPITHELIAL TUMOR OF THE YOUNG (PLNTY) von Anghileri, E, Didato, G, Deleo, F, Doniselli, F M, Moscatelli, M, Rizzi, M, Paterra, R, de Curtis, M, Farinotti, M, Freri, E, Esposito, S, Pollo, B, Silvani, A, Marucci, G

Volltext

Periventricular Nodular Heterotopia: Classification, Epileptic History, and Genesis of Epileptic Discharges von Battaglia, Giorgio, Chiapparini, Luisa, Franceschetti, Silvana, Freri, Elena, Tassi, Laura, Bassanini, Stefania, Villani, Flavio, Spreafico, Roberto, D'Incerti, Ludovico, Granata, Tiziana

Volltext

Somatic and germline mosaicisms in Severe Myoclonic Epilepsy of Infancy von Gennaro, Elena, Santorelli, Filippo M., Bertini, Enrico, Buti, Daniela, Gaggero, Roberto, Gobbi, Giuseppe, Lini, Marcella, Granata, Tiziana, Freri, Elena, Parmeggiani, Antonia, Striano, Pasquale, Veggiotti, Pierangelo, Cardinali, Simona, Bricarelli, Franca Dagna, Minetti, Carlo, Zara, Federico

Volltext

Schizencephaly: clinical spectrum, epilepsy, and pathogenesis von Granata, Tiziana, Freri, Elena, Caccia, Claudio, Setola, Veronica, Taroni, Franco, Battaglia, Giorgio

Volltext

2FC1.4 Epilepsy in girls with de novo protocadherin 19 mutations von Specchio, N., Terracciano, A., Marini, C., Trivisano, M., Mei, D., Darra, F., Bernardina, B. Dalla, Granata, T., Freri, E., Fusco, L., Guerrini, R., Bertini, E., Vigevano, F.

Volltext

P04.18 Ictal fast EEG discharges in infantile spasms, from onset to outcome von Panzica, F., Binelli, S., Granata, T., Freri, E., Visani, E., Franceschetti, S.

Volltext

Electroencephalographic Recordings of Focal Seizures in Patients Affected by Periventricular Nodular Heterotopia: Role of the Heterotopic Nodules in the Genesis of Epileptic Discha... von Battaglia, Giorgio, Franceschetti, Silvana, Chiapparini, Luisa, Freri, Elena, Bassanini, Stefania, Giavazzi, Alessio, Finardi, Adele, Taroni, Franco, Granata, Tiziana

Volltext

Familial Occurrence of Febrile Seizures and Epilepsy in Severe Myoclonic Epilepsy of Infancy (SMEI) Patients with SCN1A Mutations

Volltext