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Cognitive, adaptive, and behavioral features in Joubert syndrome.
Bulgheroni, Sara; D'Arrigo, Stefano; Signorini, Sabrina; Briguglio, Marilena; Di Sabato, Maria Lucia; Casarano, Manuela; Mancini, Francesca; Romani, Marta; Alfieri, Paolo; Battini, Roberta; Zoppello, Marina; Tortorella, Gaetano; Bertini, Enrico; Leuzzi, Vincenzo; Valente, Enza Maria; Riva, Daria.
Afiliação
  • Bulgheroni S; Developmental Neurology Division, IRCCS Fondazione Istituto Neurologico C. Besta, Milan, Italy.
  • D'Arrigo S; Developmental Neurology Division, IRCCS Fondazione Istituto Neurologico C. Besta, Milan, Italy.
  • Signorini S; Unit of Child Neurology and Psychiatry, IRCCS Fondazione Istituto Neurologico Nazionale C. Mondino, Pavia, Italy.
  • Briguglio M; Department of Pediatric, Gynecological, Microbiological and Biomedical Sciences, Unit of Infantile Neuropsychiatry, University of Messina, Messina, Italy.
  • Di Sabato ML; Department of Pediatrics and Child Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
  • Casarano M; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.
  • Mancini F; Neurogenetics Unit, Mendel Laboratory, IRCCS Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Italy.
  • Romani M; Neurogenetics Unit, Mendel Laboratory, IRCCS Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Italy.
  • Alfieri P; Unit of Child Neuropsichiatry, IRCCS Bambino Gesù Children's Hospital, Rome, Italy.
  • Battini R; Department of Developmental Neuroscience, IRCCS Fondazione Stella Maris, Pisa, Italy.
  • Zoppello M; Unit of Child Neurology and Psychiatry, IRCCS Fondazione Istituto Neurologico Nazionale C. Mondino, Pavia, Italy.
  • Tortorella G; Department of Pediatric, Gynecological, Microbiological and Biomedical Sciences, Unit of Infantile Neuropsychiatry, University of Messina, Messina, Italy.
  • Bertini E; Laboratory of Molecular Medicine, Unit of Neuromuscular and Neurodegenerative Disorders, IRCCS Bambino Gesù Pediatric Hospital, Rome, Italy.
  • Leuzzi V; Department of Pediatrics and Child Neurology and Psychiatry, Sapienza University of Rome, Rome, Italy.
  • Valente EM; Department of Medicine and Surgery, Section of Neurosciences, University of Salerno, Salerno, Italy.
  • Riva D; Neurogenetics Unit, IRCCS Santa Lucia Foundation, Rome, Italy.
Am J Med Genet A ; 170(12): 3115-3124, 2016 12.
Article em En | MEDLINE | ID: mdl-27530364
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Anormalidades Múltiplas / Cerebelo / Anormalidades do Olho / Doenças Renais Císticas / Deficiência Intelectual Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article
Texto completo
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XML
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Retina / Anormalidades Múltiplas / Cerebelo / Anormalidades do Olho / Doenças Renais Císticas / Deficiência Intelectual Tipo de estudo: Clinical_trials Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article