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Santina Città

Showing results (1-10 of 11) with videos related to

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Journal of Telemedicine and Telecare|August 19, 2007
Tele-assistance in intellectual disabilitySerafino Buono, Santina Città
Rivista Di Psichiatria|May 12, 2017
[Neuropsychological profiles, personality features and familial relational patterns in parents of children with Autism Spectrum Disorders]Marinella Zingale, Santina Città, Paola Occhipinti, et al.
Journal of Intelligence|December 22, 2023
The Intellectual Profile of Adults with Specific Learning DisabilitiesEleonora Pizzigallo, Cesare Cornoldi, Serafino Buono, et al.
Brain Sciences|August 9, 2018
Reading Deficits in Intellectual Disability Are still an Open Question: A Narrative ReviewFrancesco Domenico Di Blasi, Serafino Buono, Santina Città, et al.
American Journal of Medical Genetics. Part A|November 12, 2013
3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patientsSantina Città, Serafino Buono, Donatella Greco, et al.
European Journal of Human Genetics : EJHG|January 20, 2019
Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorderCarmela Scuderi, Lucia Saccuzzo, Mirella Vinci, et al.
Research in Developmental Disabilities|January 26, 2021
Clinical management of individuals with Intellectual Disability: The outbreak of Covid-19 pandemic as experienced in a clinical and research center Research in Developmental DisabilitiesSerafino Buono, Marinella Zingale, Santina Città, et al.
Epilepsy & Behavior : E&B|September 13, 2020
Cognitive, adaptive, and behavioral effects of adjunctive rufinamide in Lennox-Gastaut syndrome: A prospective observational clinical studyFrancesca Felicia Operto, Alberto Verrotti, Alfonso Marrelli, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
Neuromuscular Disorders : NMD|February 10, 2015
The in cis T251I and P587L POLG1 base changes: description of a new family and literature reviewCarmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Journal of Telemedicine and Telecare|August 19, 2007
Tele-assistance in intellectual disabilitySerafino Buono, Santina Città
Rivista Di Psichiatria|May 12, 2017
[Neuropsychological profiles, personality features and familial relational patterns in parents of children with Autism Spectrum Disorders]Marinella Zingale, Santina Città, Paola Occhipinti, et al.
Journal of Intelligence|December 22, 2023
The Intellectual Profile of Adults with Specific Learning DisabilitiesEleonora Pizzigallo, Cesare Cornoldi, Serafino Buono, et al.
Brain Sciences|August 9, 2018
Reading Deficits in Intellectual Disability Are still an Open Question: A Narrative ReviewFrancesco Domenico Di Blasi, Serafino Buono, Santina Città, et al.
American Journal of Medical Genetics. Part A|November 12, 2013
3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patientsSantina Città, Serafino Buono, Donatella Greco, et al.
European Journal of Human Genetics : EJHG|January 20, 2019
Biallelic intragenic duplication in ADGRB3 (BAI3) gene associated with intellectual disability, cerebellar atrophy, and behavioral disorderCarmela Scuderi, Lucia Saccuzzo, Mirella Vinci, et al.
Research in Developmental Disabilities|January 26, 2021
Clinical management of individuals with Intellectual Disability: The outbreak of Covid-19 pandemic as experienced in a clinical and research center Research in Developmental DisabilitiesSerafino Buono, Marinella Zingale, Santina Città, et al.
Epilepsy & Behavior : E&B|September 13, 2020
Cognitive, adaptive, and behavioral effects of adjunctive rufinamide in Lennox-Gastaut syndrome: A prospective observational clinical studyFrancesca Felicia Operto, Alberto Verrotti, Alfonso Marrelli, et al.
Medicina (Kaunas, Lithuania)|August 26, 2023
Specific Learning Disorders: Variation Analysis of 15 Candidate Genes in 9 Multiplex FamiliesFrancesco Calì, Francesco Domenico Di Blasi, Emanuela Avola, et al.
Neuromuscular Disorders : NMD|February 10, 2015
The in cis T251I and P587L POLG1 base changes: description of a new family and literature reviewCarmela Scuderi, Eugenia Borgione, Filippa Castello, et al.
Pageof 2