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

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

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

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Are Mutations in the DHRS9 Gene Causally Linked to Epilepsy? A Case Report by Francesco Calì, Maurizio Elia, Mirella Vinci, Luigi Vetri, Edvige Correnti, Emanuele Trapolino, Michele Roccella, Francesca Vanadia, Valentino Romano

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

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

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

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

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Italian report on RARE epilepsies (i‐RARE): A consensus on multidisciplinarity by Antonella Riva, Antonietta Coppola, Francesca Bisulli, Alberto Verrotti, Irene Bagnasco, Maurizio Elia, Francesca Darra, Simona Lattanzi, Stefano Meletti, Angela La Neve, Giancarlo Di Gennaro, Isabella Brambilla, Katia Santoro, Tommaso Prisco, Francesca Macari, Antonio Gambardella, Carlo diBonaventura, Simona Balestrini, Carla Marini, Dario Pruna, Giuseppe Capovilla, Nicola Specchio, Giuseppe Gobbi, Pasquale Striano, the iRARE Study Group

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The Italian registry for patients with Prader–Willi syndrome by Marco Salvatore, Paola Torreri, Graziano Grugni, Adele Rocchetti, Mohamad Maghnie, Giuseppa Patti, Antonino Crinò, Maurizio Elia, Donatella Greco, Corrado Romano, Adriana Franzese, Enza Mozzillo, Annamaria Colao, Gabriella Pugliese, Uberto Pagotto, Valentina Lo Preiato, Emanuela Scarano, Concetta Schiavariello, Gianluca Tornese, Danilo Fintini, Sarah Bocchini, Sara Osimani, Luisa De Sanctis, Michele Sacco, Irene Rutigliano, Maurizio Delvecchio, Maria Felicia Faienza, Malgorzata Wasniewska, Domenico Corica, Stefano Stagi, Laura Guazzarotti, Pietro Maffei, Francesca Dassie, Domenica Taruscio

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European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registry by Louise Gallagher, Michael Absoud, Miguel Castelo-Branco, Tony Charman, Maja Hempel, Richard Delorme, Guiomar Oliveira, Roberta Battini, Sven Bölte, Claire S Leblond, Thomas Bourgeron, Alexandra Lautarescu, Mercedes Serrano, Federico Vigevano, Christian P Schaaf, Bethany Oakley, Julian Tillmann, Pierre Violland, Declan G M Murphy, Sarah Douglas, Paolo Bonanni, Grainne McAlonan, Roberta Milone, Josefina Castro-Fornieles, Madeleine Bloomfield, Síofra Heraty, Roderik Plas, Anjuli Ghosh, Katrien Van den Bosch, Eliza Eaton, Ana Blázquez Hinojosa, Nadia Bolshakova, Jacqueline Borg, Sara Calderoni, Rosa Calvo Escalona, Pilar Caro, Freddy Cliquet, Alberto Danieli, Maurizio Elia, Nuno Madeira, Ciara J Molloy, Susana Mouga, Virginia Montiel, Ana Pina Rodrigues, Kristiina Tammimies, Charlotte Tye, Beatrice Mazzone, Cara O’Neill, Julie Pender, Verena Romero, Christopher Chatham

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