Ketogenic Diets in the Treatment of Epilepsy
Elia, Maurizio, Klepper, Joerg, Leiendecker, Baerbel, Hartmann, Hans
Published in Current pharmaceutical design (01.01.2017)
Published in Current pharmaceutical design (01.01.2017)
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The Role of Supplements and Over-the-Counter Products to Improve Sleep in Children: A Systematic Review
Innocenti, Alice, Lentini, Giuliana, Rapacchietta, Serena, Cinnirella, Paola, Elia, Maurizio, Ferri, Raffaele, Bruni, Oliviero
Published in International journal of molecular sciences (25.04.2023)
Published in International journal of molecular sciences (25.04.2023)
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Epilepsy in cerebrovascular diseases: Review of experimental and clinical data with meta‐analysis of risk factors
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
Published in Epilepsia (Copenhagen) (01.08.2016)
Published in Epilepsia (Copenhagen) (01.08.2016)
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Whole Exome Sequencing as a First-Line Molecular Genetic Test in Developmental and Epileptic Encephalopathies
Vetri, Luigi, Calì, Francesco, Saccone, Salvatore, Vinci, Mirella, Chiavetta, Natalia Valeria, Carotenuto, Marco, Roccella, Michele, Costanza, Carola, Elia, Maurizio
Published in International journal of molecular sciences (01.01.2024)
Published in International journal of molecular sciences (01.01.2024)
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The pharmacological management of Lennox-Gastaut syndrome and critical literature review
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
Published in Seizure (London, England) (01.12.2018)
Published in Seizure (London, England) (01.12.2018)
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A de novo ARIH2 gene mutation was detected in a patient with autism spectrum disorders and intellectual disability
Vinci, Mirella, Treccarichi, Simone, Galati Rando, Rosanna, Musumeci, Antonino, Todaro, Valeria, Federico, Concetta, Saccone, Salvatore, Elia, Maurizio, Calì, Francesco
Published in Scientific reports (09.07.2024)
Published in Scientific reports (09.07.2024)
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STXBP6 Gene Mutation: A New Form of SNAREopathy Leads to Developmental Epileptic Encephalopathy
Vinci, Mirella, Costanza, Carola, Galati Rando, Rosanna, Treccarichi, Simone, Saccone, Salvatore, Carotenuto, Marco, Roccella, Michele, Calì, Francesco, Elia, Maurizio, Vetri, Luigi
Published in International journal of molecular sciences (01.11.2023)
Published in International journal of molecular sciences (01.11.2023)
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A Genetic Variant That Disrupts MET Transcription Is Associated with Autism
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
Published in Proceedings of the National Academy of Sciences - PNAS (07.11.2006)
Published in Proceedings of the National Academy of Sciences - PNAS (07.11.2006)
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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
Treccarichi, Simone, Calì, Francesco, Vinci, Mirella, Ragalmuto, Alda, Musumeci, Antonino, Federico, Concetta, Costanza, Carola, Bottitta, Maria, Greco, Donatella, Saccone, Salvatore, Elia, Maurizio
Published in Current Issues in Molecular Biology (01.07.2024)
Published in Current Issues in Molecular Biology (01.07.2024)
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Next Generation Sequencing and Electromyography Reveal the Involvement of the P2RX6 Gene in Myopathy
Vinci, Mirella, Vitello, Girolamo Aurelio, Greco, Donatella, Treccarichi, Simone, Ragalmuto, Alda, Musumeci, Antonino, Fallea, Antonio, Federico, Concetta, Calì, Francesco, Saccone, Salvatore, Elia, Maurizio
Published in Current issues in molecular biology (01.02.2024)
Published in Current issues in molecular biology (01.02.2024)
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PLEKHG1: New Potential Candidate Gene for Periventricular White Matter Abnormalities
Calì, Francesco, Vinci, Mirella, Treccarichi, Simone, Papa, Carla, Gloria, Angelo, Musumeci, Antonino, Federico, Concetta, Vitello, Girolamo Aurelio, Nicotera, Antonio Gennaro, Di Rosa, Gabriella, Vetri, Luigi, Saccone, Salvatore, Elia, Maurizio
Published in Genes (01.08.2024)
Published in Genes (01.08.2024)
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Epilepsy: A Multifaced Spectrum Disorder
Vetri, Luigi, Roccella, Michele, Parisi, Lucia, Smirni, Daniela, Costanza, Carola, Carotenuto, Marco, Elia, Maurizio
Published in Behavioral sciences (23.01.2023)
Published in Behavioral sciences (23.01.2023)
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Journal Article
From Cannabis to Cannabidiol to Treat Epilepsy, Where Are We?
Lippiello, Pellegrino, Balestrini, Simona, Leo, Antonio, Coppola, Antonietta, Citraro, Rita, Elia, Maurizio, Russo, Emilio, De Sarro, Giovambattista
Published in Current pharmaceutical design (01.01.2016)
Published in Current pharmaceutical design (01.01.2016)
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SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis
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.
Published in Epilepsia (Copenhagen) (01.07.2009)
Published in Epilepsia (Copenhagen) (01.07.2009)
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Phenotypic Spectrum of NFIA Haploinsufficiency: Two Additional Cases and Review of the Literature
Bertini, Veronica, Cambi, Francesca, Orsini, Alessandro, Bonuccelli, Alice, Fiorini, Aureliano, Santangelo, Andrea, Scacciati, Massimo, Elia, Maurizio, Galesi, Ornella, Peroni, Diego, Valetto, Angelo
Published in Genes (30.11.2022)
Published in Genes (30.11.2022)
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Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders
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
Published in Nature communications (21.10.2020)
Published in Nature communications (21.10.2020)
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Poor School Academic Performance and Benign Epilepsy with Centro-Temporal Spikes
Vetri, Luigi, Pepi, Annamaria, Alesi, Marianna, Maltese, Agata, Scifo, Lidia, Roccella, Michele, Quatrosi, Giuseppe, Elia, Maurizio
Published in Behavioral sciences (28.01.2023)
Published in Behavioral sciences (28.01.2023)
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Sensory Profiles of Children with Autism Spectrum Disorder with and without Feeding Problems: A Comparative Study in Sicilian Subjects
Panerai, Simonetta, Ferri, Raffaele, Catania, Valentina, Zingale, Marinella, Ruccella, Daniela, Gelardi, Donatella, Fasciana, Daniela, Elia, Maurizio
Published in Brain sciences (31.05.2020)
Published in Brain sciences (31.05.2020)
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Electroclinical Features of Epilepsy in Mucopolysaccharidosis III: Outcome Description in a Cohort of 15 Italian Patients
Barone, Rita, Fiumara, Agata, Gulisano, Mariangela, Cirnigliaro, Lara, Cocuzza, Maria Donatella, Guida, Claudia, Pettinato, Fabio, Greco, Filippo, Elia, Maurizio, Rizzo, Renata
Published in Frontiers in neurology (19.07.2021)
Published in Frontiers in neurology (19.07.2021)
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