O073. Proposal guidelines for epilepsy and headache

von Dainese, Filippo, Avanzini, Giuliano, La Neve, Angela, Pruna, Dario, Paladin, Francesco
Veröffentlicht in J Headache Pain (2015)

Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment

von Rodenas-Cuadrado, Pedro, Pietrafusa, Nicola, Francavilla, Teresa, La Neve, Angela, Striano, Pasquale, Vernes, Sonja C.
Veröffentlicht in BMC Med Genet (2016)

Do neurologists agree in diagnosing drug resistance in adults with focal epilepsy?

von Zaccara, Gaetano, Mula, Marco, Ferrò, Bruno, Consoli, Domenico, Elia, Maurizio, Giallonardo, Anna Teresa, Iudice, Alfonso, La Neve, Angela, Meletti, Stefano, Tinuper, Paolo, Zummo, Leila, Perucca, Emilio
Veröffentlicht in Epilepsia (2018)

The clinical phenotype of autosomal dominant lateral temporal lobe epilepsy related to reelin mutations

von Michelucci, Roberto, Pulitano, Patrizia, Di Bonaventura, Carlo, Binelli, Simona, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Serioli, Elena, Dazzo, Emanuela, Fanciulli, Manuela, Nobile, Carlo
Veröffentlicht in Epilepsy Behav (2017)

Progressive myoclonic epilepsies: Definitive and still undetermined causes

von Franceschetti, Silvana, Michelucci, Roberto, Canafoglia, Laura, Striano, Pasquale, Gambardella, Antonio, Magaudda, Adriana, Tinuper, Paolo, La Neve, Angela, Ferlazzo, Edoardo, Gobbi, Giuseppe, Giallonardo, Anna Teresa, Capovilla, Giuseppe, Visani, Elisa, Panzica, Ferruccio, Avanzini, Giuliano, Tassinari, Carlo Alberto, Bianchi, Amedeo, Zara, Federico
Veröffentlicht 2014

ADAM23, a Gene Related to LGI1, Is Not Linked to Autosomal Dominant Lateral Temporal Epilepsy

von Rigon, Laura, Vettori, Andrea, Busolin, Giorgia, Egeo, Gabriella, Pulitano, Patrizia, Santulli, Lia, Pasini, Elena, Striano, Pasquale, la Neve, Angela, Vianello Dri, Valeria, Boniver, Clementina, Gambardella, Antonio, Banfi, Paola, Binelli, Simona, Di Bonaventura, Carlo, Striano, Salvatore, de Falco, Fabrizio, Giallonardo, Anna T., Mecarelli, Oriano, Michelucci, Roberto, Nobile, Carlo
Veröffentlicht 2011

Heterozygous Reelin Mutations Cause Autosomal-Dominant Lateral Temporal Epilepsy

von Dazzo, Emanuela, Fanciulli, Manuela, Serioli, Elena, Minervini, Giovanni, Pulitano, Patrizia, Binelli, Simona, Di Bonaventura, Carlo, Luisi, Concetta, Pasini, Elena, Striano, Salvatore, Striano, Pasquale, Coppola, Giangennaro, Chiavegato, Angela, Radovic, Slobodanka, Spadotto, Alessandro, Uzzau, Sergio, La Neve, Angela, Giallonardo, Anna Teresa, Mecarelli, Oriano, Tosatto, Silvio C.E., Ottman, Ruth, Michelucci, Roberto, Nobile, Carlo
Veröffentlicht in Am J Hum Genet (2015)

Results From an Italian Expanded Access Program on Cannabidiol Treatment in Highly Refractory Dravet Syndrome and Lennox–Gastaut Syndrome

von Iannone, Luigi Francesco, Arena, Gabriele, Battaglia, Domenica, Bisulli, Francesca, Bonanni, Paolo, Boni, Antonella, Canevini, Maria Paola, Cantalupo, Gaetano, Cesaroni, Elisabetta, Contin, Manuela, Coppola, Antonietta, Cordelli, Duccio Maria, Cricchiuti, Giovanni, De Giorgis, Valentina, De Leva, Maria Fulvia, De Rinaldis, Marta, d'Orsi, Giuseppe, Elia, Maurizio, Galimberti, Carlo Andrea, Morano, Alessandra, Granata, Tiziana, Guerrini, Renzo, Lodi, Monica A. M., La Neve, Angela, Marchese, Francesca, Masnada, Silvia, Michelucci, Roberto, Nosadini, Margherita, Pilolli, Nicola, Pruna, Dario, Ragona, Francesca, Rosati, Anna, Santucci, Margherita, Spalice, Alberto, Pietrafusa, Nicola, Striano, Pasquale, Tartara, Elena, Tassi, Laura, Papa, Amanda, Zucca, Claudio, Russo, Emilio, Mecarelli, Oriano
Veröffentlicht in Front Neurol (2021)