Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias von Garone, Giacomo, Capuano, Alessandro, Travaglini, Lorena, Graziola, Federica, Stregapede, Fabrizia, Zanni, Ginevra, Vigevano, Federico, Bertini, Enrico, Nicita, Francesco

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Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical review von Schirinzi, Tommaso, Garone, Giacomo, Travaglini, Lorena, Vasco, Gessica, Galosi, Serena, Rios, Loreto, Castiglioni, Claudia, Barassi, Claudia, Battaglia, Domenica, Gambardella, Maria Luigia, Cantonetti, Laura, Graziola, Federica, Marras, Carlo Efisio, Castelli, Enrico, Bertini, Enrico, Capuano, Alessandro, Leuzzi, Vincenzo

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Impact of Italian lockdown on Tourette's syndrome patients at the time of the COVID‐19 pandemic von Graziola, Federica, Garone, Giacomo, Di Criscio, Lorena, Grasso, Melissa, Curatolo, Paolo, Vigevano, Federico, Capuano, Alessandro

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Diagnostic Yield of a Targeted Next-Generation Sequencing Gene Panel for Pediatric-Onset Movement Disorders: A 3-Year Cohort Study von Graziola, Federica, Garone, Giacomo, Stregapede, Fabrizia, Bosco, Luca, Vigevano, Federico, Curatolo, Paolo, Bertini, Enrico, Travaglini, Lorena, Capuano, Alessandro

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Pediatric torticollis: clinical report and predictors of urgency of 1409 cases von Raucci, Umberto, Roversi, Marco, Ferretti, Alessandro, Faccia, Valerio, Garone, Giacomo, Panetta, Fabio, Mariani, Carlo, Rizzotto, Eloisa, Torelli, Antonio, Colafati, Giovanna Stefania, Aulisa, Angelo Gabriele, Parisi, Pasquale, Villani, Alberto

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Dyskinetic crisis in GNAO1 -related disorders: clinical perspectives and management strategies von Domínguez Carral, Jana, Reinhard, Carola, Ebrahimi-Fakhari, Darius, Dorison, Nathalie, Galosi, Serena, Garone, Giacomo, Malenica, Masa, Ravelli, Claudia, Serdaroglu, Esra, van de Pol, Laura A, Koy, Anne, Leuzzi, Vincenzo, Roubertie, Agathe, Lin, Jean-Pierre, Doummar, Diane, Cif, Laura, Ortigoza-Escobar, Juan Darío

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Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region von Nicita, Francesco, Garone, Giacomo, Spalice, Alberto, Savasta, Salvatore, Striano, Pasquale, Pantaleoni, Chiara, Spartà, Maria Valentina, Kluger, Gerhard, Capovilla, Giuseppe, Pruna, Dario, Freri, Elena, D'Arrigo, Stefano, Verrotti, Alberto

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Case Report: A rare form of congenital erythrocytosis due to SLC30A10 biallelic variants-differential diagnosis and recommendation for biochemical and genetic screening von Giannini, Rosalinda, Agolini, Emanuele, Palumbo, Giuseppe, Novelli, Antonio, Garone, Giacomo, Grasso, Melissa, Colafati, Giovanna Stefania, Matraxia, Marta, Piccirilli, Eleonora, Deodati, Annalisa, Ceglie, Giulia

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Early Myoclonic Encephalopathy in 9q33‐q34 Deletion Encompassing STXBP1 and SPTAN1 von Nicita, Francesco, Ulgiati, Fiorenza, Bernardini, Laura, Garone, Giacomo, Papetti, Laura, Novelli, Antonio, Spalice, Alberto

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Acute Pupillary Disorders in Children: A 10-Year Retrospective Study of 101 Patients von Garone, Giacomo, Roversi, Marco, Pisani, Mara, La Penna, Francesco, Musolino, Antonio, Cristaldi, Sebastian, Musolino, Anna Maria, Roberto, Amanda, Petrocelli, Gianni, Reale, Antonino, Midulla, Fabio, Villani, Alberto, Raucci, Umberto

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A cohort study on acute ocular motility disorders in pediatric emergency department von Raucci, Umberto, Parisi, Pasquale, Vanacore, Nicola, Ferro, Valentina, Garone, Giacomo, Sancetta, Federica, Petroni, Sergio, Pro, Stefano, Rossi, Rossella, Reale, Antonino, Pirozzi, Nicola

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Working memory, attention and planning abilities in NKX2.1-related chorea von Graziola, Federica, Garone, Giacomo, Grasso, Melissa, Schirinzi, Tommaso, Capuano, Alessandro

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Alternating Hemiplegia of Childhood: Understanding the Genotype-Phenotype Relationship of ATP1A3 Variations von Capuano, Alessandro, Garone, Giacomo, Tiralongo, Giuseppe, Graziola, Federica

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Reply to: “GNAO1 Haploinsufficiency Associated with a Mild Delayed‐Onset Dystonia Phenotype” von Wirth, Thomas, Garone, Giacomo, Kurian, Manju A., Piton, Amélie, Roze, Emmanuel, Lin, Jean Pierre, Tranchant, Christine, Cif, Laura, Doummar, Diane, Anheim, Mathieu

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Cognitive Assessment in GNAO1 Neurodevelopmental Disorder Using an Eye Tracking System von Graziola, Federica, Garone, Giacomo, Grasso, Melissa, Capuano, Alessandro

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Movement Disorders in Patients With Genetic Developmental and Epileptic Encephalopathies von van der Veen, Sterre, Tse, Gabrielle T W, Ferretti, Alessandro, Garone, Giacomo, Post, Bart, Specchio, Nicola, Fung, Victor S C, Trivisano, Marina, Scheffer, Ingrid E

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Prestatus and status dystonicus in children and adolescents von Garone, Giacomo, Graziola, Federica, Nicita, Francesco, Frascarelli, Flaminia, Randi, Franco, Zazza, Marco, Cantonetti, Laura, Cossu, Silvia, Marras, Carlo Efisio, Capuano, Alessandro

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Acute Movement Disorders in Childhood von Garone, Giacomo, Graziola, Federica, Grasso, Melissa, Capuano, Alessandro

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Highlighting the Dystonic Phenotype Related to GNAO1 von Wirth, Thomas, Garone, Giacomo, Kurian, Manju A., Piton, Amélie, Millan, Francisca, Telegrafi, Aida, Drouot, Nathalie, Rudolf, Gabrielle, Chelly, Jamel, Marks, Warren, Burglen, Lydie, Demailly, Diane, Coubes, Phillipe, Castro‐Jimenez, Mayte, Joriot, Sylvie, Ghoumid, Jamal, Belin, Jérémie, Faucheux, Jean‐Marc, Blumkin, Lubov, Hull, Mariam, Parnes, Mered, Ravelli, Claudia, Poulen, Gaëtan, Calmels, Nadège, Nemeth, Andrea H., Smith, Martin, Barnicoat, Angela, Ewenczyk, Claire, Méneret, Aurélie, Roze, Emmanuel, Keren, Boris, Mignot, Cyril, Beroud, Christophe, Acosta, Fernando, Nowak, Catherine, Wilson, William G., Steel, Dora, Capuano, Alessandro, Vidailhet, Marie, Lin, Jean‐Pierre, Tranchant, Christine, Cif, Laura, Doummar, Diane, Anheim, Mathieu

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A novel KCTD17 mutation is associated with childhood early-onset hyperkinetic movement disorder von Graziola, Federica, Stregapede, Fabrizia, Travaglini, Lorena, Garone, Giacomo, Verardo, Margherita, Bosco, Luca, Pro, Stefano, Bertini, Enrico, Curatolo, Paolo, Vigevano, Federico, Capuano, Alessandro

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