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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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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Role of COMT V158M Polymorphism in the Development of Dystonia after Administration of Antipsychotic Drugs von Nicotera, Antonio Gennaro, Di Rosa, Gabriella, Turriziani, Laura, Costanzo, Maria Cristina, Stracuzzi, Emanuela, Vitello, Girolamo Aurelio, Rando, Rosanna Galati, Musumeci, Antonino, Vinci, Mirella, Musumeci, Sebastiano Antonino, Calì, Francesco

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Killer-specific secretory (Ksp37) gene expression in subjects with Down’s syndrome von Salemi, Michele, Barone, Concetta, Morale, Maria Concetta, Caniglia, Salvatore, Romano, Carmelo, Salluzzo, Maria Grazia, Rando, Rosanna G. Galati, Ragalmuto, Alda, Bosco, Paolo, Romano, Corrado

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Poly (ADP-ribose) polymerase-1 (PARP-1) − 410C/T polymorphism in Sicilian patients with Parkinson's disease von Salluzzo, Maria Grazia, Cosentino, Filomena I, Romano, Carmelo, Scillato, Francesco, Morale, Maria Concetta, Rando, Rosanna Galati, Elia, Federica, Spada, Rosario S, Bosco, Paolo, Salemi, Michele

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