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Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome.
Montanaro, Federica Alice Maria; Alfieri, Paolo; Caciolo, Cristina; Cumbo, Francesca; Piga, Simone; Tartaglia, Marco; Licchelli, Serena; Digilio, Maria Cristina; Vicari, Stefano.
Afiliación
  • Montanaro FAM; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Alfieri P; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Caciolo C; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Cumbo F; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Piga S; Unit of Muscular and Neurodegenerative Disorders, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Tartaglia M; Clinical Epidemiology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Licchelli S; Genetics and Rare Diseases Research Division, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Digilio MC; Child and Adolescent Neuropsychiatry Unit, Department of Neuroscience, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Vicari S; Fondazione UILDM Lazio Onlus, Rome, Italy.
Am J Med Genet C Semin Med Genet ; 190(4): 510-519, 2022 12.
Article en En | MEDLINE | ID: mdl-36490374
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Síndrome de Noonan Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Italia
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastorno por Déficit de Atención con Hiperactividad / Síndrome de Noonan Límite: Female / Humans / Male Idioma: En Revista: Am J Med Genet C Semin Med Genet Asunto de la revista: GENETICA MEDICA Año: 2022 Tipo del documento: Article País de afiliación: Italia