Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Santina Città"'
Autor:
Eleonora Pizzigallo, Cesare Cornoldi, Serafino Buono, Santina Città, Francesco Viola, Enrico Toffalini
Publikováno v:
Journal of Intelligence, Vol 11, Iss 12, p 223 (2023)
Despite growing research on adults with specific learning disabilities (SLDs), evidence concerning their intellectual profile remains scarce. The present study examined the results of the administration of the Wechsler Adult Intelligence Scale—Four
Externí odkaz:
https://doaj.org/article/39526917fd2447c39c965b7687da8018
Autor:
Francesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, Mirella Vinci, Antonino Musumeci, Angelo Gloria, Donatella Greco, Daniela Rita Raciti, Alessandro Zagami, Biagio Rizzo, Santina Città, Concetta Federico, Luigi Vetri, Salvatore Saccone, Serafino Buono
Publikováno v:
Medicina, Vol 59, Iss 8, p 1503 (2023)
Background and Objectives: Specific Learning Disorder (SLD) is a complex neurobiological disorder characterized by a persistent difficult in reading (dyslexia), written expression (dysgraphia), and mathematics (dyscalculia). The hereditary and geneti
Externí odkaz:
https://doaj.org/article/c52658657864431d919bb3b9d79f8f4a
Autor:
Francesco Domenico Di Blasi, Serafino Buono, Santina Città, Angela Antonia Costanzo, Pierluigi Zoccolotti
Publikováno v:
Brain Sciences, Vol 8, Iss 8, p 146 (2018)
Background. In children with intellectual disability (ID), the acquisition of reading skills constitutes a basic step towards the possibility of independent living, social inclusion and participation. Methods. We carried out a narrative review of the
Externí odkaz:
https://doaj.org/article/20b03571d0c3469799e8c1cc27e13ef7
Autor:
Raffaele Ferri, Paola Occhipinti, Donatella Greco, Grazia Trubia, Giovanna Mascali, Santina Città, Marinella Zingale, Catalda Gagliano, Vita Mongelli, Enrica Pettinato, Serafino Buono
Publikováno v:
Research in Developmental Disabilities
During the COVID-19 pandemic, the Oasi Research Institute of Troina (Italy) became an important hotbed for infection; in fact, 109 patients with different levels of Intellectual Disability (ID) tested positive for COVID-19. The procedures and interve
Autor:
Teresa Mattina, Lucia Saccuzzo, Santina Città, Lucia Castiglia, Marco Fichera, Michele Salemi, Corrado Romano, Mirella Vinci, Carmela Scuderi, Eugenia Borgione, Ornella Galesi
In recent years, chromosomal microarray analysis has permitted the discovery of rearrangements underlying several neurodevelopmental disorders and still represents the first diagnostic test for unexplained neurodevelopmental disabilities. Here we rep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc0e8301b0ee7d9a41a71ef0294f88b4
http://hdl.handle.net/20.500.11769/359702
http://hdl.handle.net/20.500.11769/359702
Publikováno v:
Rivista di psichiatria. 52(2)
The study of neuropsychological profiles and personality features of parents of persons with Autism Spectrum Disorder (ASD) has highlighted specific traits that turned out to be useful for diagnostic purposes.In our study, psychodiagnostic measures h
Autor:
Serafino Buono, Enrico Alfei, Sara Bulgheroni, Corrado Romano, Concetta Barone, Chiara Pantaleoni, Santina Città, Donatella Greco, Arianna Usilla
Publikováno v:
American Journal of Medical Genetics Part A. 161:3018-3022
The 3q29 microdeletion syndrome is a rare, recurrent genomic disorder, associated with a variable phenotype, despite the same deletion size, consisting in neurodevelopmental features, such as intellectual disability (ID), schizophrenia, autism, bipol
Autor:
Serafino Buono, Santina Città
Publikováno v:
Journal of telemedicine and telecare. 13(5)
We conducted a trial of multidisciplinary tele-assistance to support 20 families of patients with intellectual disability. Psychological, educational, social and medical support was provided by videoconferencing, email and on-line sharing of diagnost
Autor:
Claudio Zucca, Michela Sole, Pasquale Striano, Francesca Felicia Operto, Grazia Maria Giovanna Pastorino, Alfonso Marrelli, Alberto Verrotti, Santina Città, Roberta Ciuffini, Giangennaro Coppola, Maurizio Elia, Valentina Manfredi
Introduction Lennox–Gastaut syndrome (LGS) is a severe pediatric epilepsy syndrome characterized by multiple drug-resistant seizure types. Children with LGS usually experience cognitive regression, and LGS is almost always associated with moderate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec555dd2cee5ea5e6b607e5b8a60e528
http://hdl.handle.net/11567/1027665
http://hdl.handle.net/11567/1027665
Publikováno v:
Publons
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::0bc08ac9f5ec8c4f6ec0e6da3a2be9e9
https://publons.com/publon/14332001/
https://publons.com/publon/14332001/