Myoclonic status in nonprogressive encephalopathies: An update von Elia, Maurizio

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The Role of Supplements and Over-the-Counter Products to Improve Sleep in Children: A Systematic Review von Innocenti, Alice, Lentini, Giuliana, Rapacchietta, Serena, Cinnirella, Paola, Elia, Maurizio, Ferri, Raffaele, Bruni, Oliviero

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Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta‐analysis of risk factors von Ferlazzo, Edoardo, Gasparini, Sara, Beghi, Ettore, Sueri, Chiara, Russo, Emilio, Leo, Antonio, Labate, Angelo, Gambardella, Antonio, Belcastro, Vincenzo, Striano, Pasquale, Paciaroni, Maurizio, Pisani, Laura Rosa, Aguglia, Umberto, Aloisi, Paolo, Arcudi, Luciano, Benna, Paolo, Bianchi, Amedeo, Bogliun, Graziella, Buttinelli, Carla, Campostrini, Roberto, Cantello, Roberto, Cianci, Vittoria, Consoli, Domenico, Coppola, Antonietta, Costanzo, Erminio, De Falco, Fabrizio Antonio, De Maria, Giovanni, Elia, Maurizio, Franceschetti, Silvana, Galimberti, Carlo Andrea, Giallonardo, Anna Teresa, Gigli, Gian Luigi, Iannacchero, Rosario, Iudice, Alfonso, La Neve, Angela, Latella, Maria Adele, Le Piane, Emilio, Magaudda, Adriana, Marciani, Maria Grazia, Maschio, Marta, Mecarelli, Oriano, Michelucci, Roberto, Minicucci, Fabio, Moglia, Arrigo, Monti, Fabrizio, Mumoli, Laura, Musolino, Rosa, Nozzoli, Cecilia, Paciello, Nicola, Paladin, Francesco, Palumbo, Pasquale, Pisani, Francesco, Primavera, Alberto, Rocchi, Raffaele, Sartucci, Ferdinando, Sasanelli, Francesco, Silvestri, Rosalia, Sofia, Vito, Specchio, Luigi M, Striano, Salvatore, Tinuper, Paolo, Villani, Flavio, Zaccara, Gaetano

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Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies von Vetri, Luigi, Calì, Francesco, Saccone, Salvatore, Vinci, Mirella, Chiavetta, Natalia Valeria, Carotenuto, Marco, Roccella, Michele, Costanza, Carola, Elia, Maurizio

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The pharmacological management of Lennox-Gastaut syndrome and critical literature review von Verrotti, Alberto, Striano, Pasquale, Iapadre, Giulia, Zagaroli, Luca, Bonanni, Paolo, Coppola, Giangennaro, Elia, Maurizio, Mecarelli, Oriano, Franzoni, Emilio, Liso, Paola De, Vigevano, Federico, Curatolo, Paolo

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STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy von Vinci, Mirella, Costanza, Carola, Galati Rando, Rosanna, Treccarichi, Simone, Saccone, Salvatore, Carotenuto, Marco, Roccella, Michele, Calì, Francesco, Elia, Maurizio, Vetri, Luigi

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A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability von Vinci, Mirella, Treccarichi, Simone, Galati Rando, Rosanna, Musumeci, Antonino, Todaro, Valeria, Federico, Concetta, Saccone, Salvatore, Elia, Maurizio, Calì, Francesco

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CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy von Dell’Isola, Giovanni Battista, Fattorusso, Antonella, Pisani, Francesco, Mastrangelo, Mario, Cordelli, Duccio Maria, Pavone, Piero, Parisi, Pasquale, Ferretti, Alessandro, Operto, Francesca Felicia, Elia, Maurizio, Carotenuto, Marco, Pruna, Dario, Matricardi, Sara, Spezia, Elisabetta, Spalice, Alberto, Scorrano, Giovanna, Savasta, Salvatore, Prontera, Paolo, Di Cara, Giuseppe, Fruttini, Daniela, Salpietro, Vincenzo, Striano, Pasquale, Verrotti, Alberto

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A Genetic Variant That Disrupts MET Transcription Is Associated with Autism von Campbell, Daniel B., Sutcliffe, James S., Ebert, Philip J., Militerni, Roberto, Bravaccio, Carmela, Trillo, Simona, Elia, Maurizio, Schneider, Cindy, Melmed, Raun, Sacco, Roberto, Persico, Antonio M., Levitt, Pat

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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders von Gillentine, Madelyn A., Wang, Tianyun, Hoekzema, Kendra, Rosenfeld, Jill, Liu, Pengfei, Guo, Hui, Kim, Chang N., De Vries, Bert B. A., Vissers, Lisenka E. L. M., Nordenskjold, Magnus, Kvarnung, Malin, Lindstrand, Anna, Nordgren, Ann, Gecz, Jozef, Iascone, Maria, Cereda, Anna, Scatigno, Agnese, Maitz, Silvia, Zanni, Ginevra, Bertini, Enrico, Zweier, Christiane, Schuhmann, Sarah, Wiesener, Antje, Pepper, Micah, Panjwani, Heena, Torti, Erin, Abid, Farida, Anselm, Irina, Srivastava, Siddharth, Atwal, Paldeep, Bacino, Carlos A., Bhat, Gifty, Cobian, Katherine, Bird, Lynne M., Friedman, Jennifer, Wright, Meredith S., Callewaert, Bert, Petit, Florence, Mathieu, Sophie, Afenjar, Alexandra, Christensen, Celenie K., White, Kerry M., Elpeleg, Orly, Berger, Itai, Espineli, Edward J., Fagerberg, Christina, Brasch-Andersen, Charlotte, Hansen, Lars Kjaersgaard, Feyma, Timothy, Hughes, Susan, Thiffault, Isabelle, Sullivan, Bonnie, Yan, Shuang, Keller, Kory, Keren, Boris, Mignot, Cyril, Kooy, Frank, Meuwissen, Marije, Basinger, Alice, Kukolich, Mary, Philips, Meredith, Ortega, Lucia, Drummond-Borg, Margaret, Lauridsen, Mathilde, Sorensen, Kristina, Lehman, Anna, Lopez-Rangel, Elena, Levy, Paul, Lessel, Davor, Lotze, Timothy, Madan-Khetarpal, Suneeta, Sebastian, Jessica, Vento, Jodie, Vats, Divya, Benman, L. Manace, Mckee, Shane, Mirzaa, Ghayda M., Muss, Candace, Pappas, John, Peeters, Hilde, Romano, Corrado, Elia, Maurizio, Galesi, Ornella, Simon, Marleen E. H., van Gassen, Koen L. I., Simpson, Kara, Stratton, Robert, Syed, Sabeen, Thevenon, Julien, Palafoll, Irene Valenzuela, Vitobello, Antonio, Bournez, Marie, Faivre, Laurence, Xia, Kun, Earl, Rachel K., Nowakowski, Tomasz, Bernier, Raphael A., Eichler, Evan E.

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Implications of a De Novo Variant in the SOX12 Gene in a Patient with Generalized Epilepsy, Intellectual Disability, and Childhood Emotional Behavioral Disorders von Treccarichi, Simone, Calì, Francesco, Vinci, Mirella, Ragalmuto, Alda, Musumeci, Antonino, Federico, Concetta, Costanza, Carola, Bottitta, Maria, Greco, Donatella, Saccone, Salvatore, Elia, Maurizio

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An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy von Elia, Maurizio, Amato, Carmelo, Bottitta, Maria, Grillo, Lucia, Calabrese, Giuseppe, Esposito, Maria, Carotenuto, Marco

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Next Generation Sequencing and Electromyography Reveal the Involvement of the P2RX6 Gene in Myopathy von Vinci, Mirella, Vitello, Girolamo Aurelio, Greco, Donatella, Treccarichi, Simone, Ragalmuto, Alda, Musumeci, Antonino, Fallea, Antonio, Federico, Concetta, Calì, Francesco, Saccone, Salvatore, Elia, Maurizio

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Epilepsy: A Multifaced Spectrum Disorder von Vetri, Luigi, Roccella, Michele, Parisi, Lucia, Smirni, Daniela, Costanza, Carola, Carotenuto, Marco, Elia, Maurizio

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SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis von Marini, Carla, Scheffer, Ingrid E., Nabbout, Rima, Mei, Davide, Cox, Kathy, Dibbens, Leanne M., McMahon, Jacinta M., Iona, Xenia, Carpintero, Rochio Sanchez, Elia, Maurizio, Cilio, Maria Roberta, Specchio, Nicola, Giordano, Lucio, Striano, Pasquale, Gennaro, Elena, Cross, J. Helen, Kivity, Sara, Neufeld, Miriam Y., Afawi, Zaid, Andermann, Eva, Keene, Daniel, Dulac, Olivier, Zara, Federico, Berkovic, Samuel F., Guerrini, Renzo, Mulley, John C.

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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders von Wang, Tianyun, Hoekzema, Kendra, Vecchio, Davide, Wu, Huidan, Sulovari, Arvis, Coe, Bradley P., Gillentine, Madelyn A., Wilfert, Amy B., Perez-Jurado, Luis A., Kvarnung, Malin, Sleyp, Yoeri, Earl, Rachel K., Rosenfeld, Jill A., Geisheker, Madeleine R., Han, Lin, Du, Bing, Barnett, Chris, Thompson, Elizabeth, Shaw, Marie, Carroll, Renee, Friend, Kathryn, Catford, Rachael, Palmer, Elizabeth E., Zou, Xiaobing, Ou, Jianjun, Li, Honghui, Guo, Hui, Gerdts, Jennifer, Avola, Emanuela, Calabrese, Giuseppe, Elia, Maurizio, Greco, Donatella, Lindstrand, Anna, Nordgren, Ann, Anderlid, Britt-Marie, Vandeweyer, Geert, Van Dijck, Anke, Van der Aa, Nathalie, McKenna, Brooke, Hancarova, Miroslava, Bendova, Sarka, Havlovicova, Marketa, Malerba, Giovanni, Bernardina, Bernardo Dalla, Muglia, Pierandrea, van Haeringen, Arie, Hoffer, Mariette J. V., Franke, Barbara, Cappuccio, Gerarda, Delatycki, Martin, Lockhart, Paul J., Manning, Melanie A., Liu, Pengfei, Scheffer, Ingrid E., Brunetti-Pierri, Nicola, Rommelse, Nanda, Amaral, David G., Santen, Gijs W. E., Trabetti, Elisabetta, Sedláček, Zdeněk, Michaelson, Jacob J., Pierce, Karen, Courchesne, Eric, Kooy, R. Frank, Nordenskjöld, Magnus, Romano, Corrado, Peeters, Hilde, Bernier, Raphael A., Gecz, Jozef, Xia, Kun, Eichler, Evan E.

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Sensory Profiles of Children with Autism Spectrum Disorder with and without Feeding Problems: A Comparative Study in Sicilian Subjects von Panerai, Simonetta, Ferri, Raffaele, Catania, Valentina, Zingale, Marinella, Ruccella, Daniela, Gelardi, Donatella, Fasciana, Daniela, Elia, Maurizio

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Poor School Academic Performance and Benign Epilepsy with Centro-Temporal Spikes von Vetri, Luigi, Pepi, Annamaria, Alesi, Marianna, Maltese, Agata, Scifo, Lidia, Roccella, Michele, Quatrosi, Giuseppe, Elia, Maurizio

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EEG Patterns in Patients with Prader-Willi Syndrome von Elia, Maurizio, Rutigliano, Irene, Sacco, Michele, Madeo, Simona F., Wasniewska, Malgorzata, Li Pomi, Alessandra, Trifiro, Giuliana, Di Bella, Paolo, De Lucia, Silvana, Vetri, Luigi, Iughetti, Lorenzo, Delvecchio, Maurizio

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Lacosamide in pediatric and adult patients: Comparison of efficacy and safety von Verrotti, Alberto, Loiacono, Giulia, Pizzolorusso, Antonella, Parisi, Pasquale, Bruni, Oliviero, Luchetti, Anna, Zamponi, Nelia, Cappanera, Silvia, Grosso, Salvatore, Kluger, Gerhard, Janello, Christine, Franzoni, Emilio, Elia, Maurizio, Spalice, Alberto, Coppola, Giangennaro, Striano, Pasquale, Pavone, Piero, Savasta, Salvatore, Viri, Maurizio, Romeo, Antonino, Aloisi, Paolo, Gobbi, Giuseppe, Ferretti, Alessandro, Cusmai, Raffaella, Curatolo, Paolo

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