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Clinical Linguistics & Phonetics|October 17, 2017
Early communicative skills of children with Klinefelter syndromeLaura Zampini, Tiziana Burla, Gaia Silibello, et al.Research in Developmental Disabilities|April 25, 2022
Age-related hallmarks of psychopathology in Cornelia de Lange and Rubinstein-Taybi syndromesLudovica Giani, Giovanni Michelini, Paola Francesca Ajmone, et al.Journal of Psychiatric Research|August 7, 2025
Executive function deficits as risk markers for psychopathology and autism related traits in cornelia de lange and rubinstein-Taybi syndromesLudovica Giani, Giovanni Michelini, Paola Francesca Ajmone, et al.Journal of Child Neurology|September 26, 2013
Think about it: FMR1 gene mosaicismFrancesca Andrea Bonarrigo, Silvia Russo, Paola Vizziello, et al.Minerva Pediatrica|March 24, 2016
Klinefelter Syndrome in preschool children: the importance of an early multidisciplinary approach for patients and familiesClaudia Rigamonti, Paola Vizziello, Federico Monti, et al.Journal of Speech, Language, and Hearing Research : JSLHR|July 21, 2021
Irony Comprehension in Children With Cochlear Implants: The Role of Language Competence, Theory of Mind, and Prosody RecognitionFrancesca Panzeri, Sara Cavicchiolo, Beatrice Giustolisi, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 8, 2014
Communication, cognitive development and behavior in children with Cornelia de Lange Syndrome (CdLS): preliminary resultsPaola Francesca Ajmone, Claudia Rigamonti, Francesca Dall'Ara, et al.International Journal of Language & Communication Disorders|July 21, 2017
Vocal and gestural productions of 24-month-old children with sex chromosome trisomiesLaura Zampini, Lara Draghi, Gaia Silibello, et al.Italian Journal of Pediatrics|October 5, 2012
Early manifestations in a cohort of children prenatally diagnosed with 47,XYY. Role of multidisciplinary counseling for parental guidance and prevention of aggressive behaviorFaustina Lalatta, Emanuela Folliero, Ugo Cavallari, et al.American Journal of Medical Genetics. Part A|May 23, 2013
Healthcare transition in patients with rare genetic disorders with and without developmental disability: neurofibromatosis 1 and Williams-Beuren syndromeAndrea Van Lierde, Francesca Menni, Maria Francesca Bedeschi, et al.Pageof 2