Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Flavia Cirillo"'
Autor:
Elisa Fucà, Flavia Cirillo, Laura Celestini, Paolo Alfieri, Diletta Valentini, Floriana Costanzo, Stefano Vicari
Publikováno v:
Frontiers in Psychiatry, Vol 13 (2023)
IntroductionChildren and adolescents with intellectual disability (ID) exhibit higher rates of oppositional defiant disorder (ODD) than typically developing (TD) peers. However, studies focusing on the investigation of ODD prevalence in youth with Do
Externí odkaz:
https://doaj.org/article/f9f049bd34f14efcaa9e636aa5cff2ee
Autor:
Paolo Alfieri, Francesca Cumbo, Giulia Serra, Monia Trasolini, Camilla Frattini, Francesco Scibelli, Serena Licchelli, Flavia Cirillo, Cristina Caciolo, Maria Pia Casini, Adele D’Amico, Marco Tartaglia, Maria Cristina Digilio, Rossella Capolino, Stefano Vicari
Publikováno v:
Brain Sciences, Vol 11, Iss 2, p 233 (2021)
Noonan syndrome (NS) is a dominant clinically variable and genetically heterogeneous developmental disorder caused by germ-line mutations encoding components of the Ras–MAPK signaling pathway. A few studies have investigated psychopathological feat
Externí odkaz:
https://doaj.org/article/29dfd9051c164f5f831e577089260789
Autor:
Paola De Rose, Fortunata Salvaguardia, Paola Bergonzini, Flavia Cirillo, Francesco Demaria, Maria Pia Casini, Deny Menghini, Stefano Vicari
Publikováno v:
The Scientific World Journal, Vol 2016 (2016)
The aim of the present study is to evaluate the current psychopathological problems of different forms associated with maltreatment on children’s and adolescents’ mental health. Ninety-five females and ninety males with a mean age of 8.8 years wh
Externí odkaz:
https://doaj.org/article/21b7a33fad0c4f1d8f79ac11381b8843
Autor:
Francesca Cumbo, Flavia Cirillo, Paolo Alfieri, Maria Pia Casini, Rossella Capolino, Monia Trasolini, Serena Licchelli, Giulia Serra, Francesco Scibelli, Maria Cristina Digilio, Adele D'Amico, Marco Tartaglia, Camilla Frattini, Stefano Vicari, Cristina Caciolo
Publikováno v:
Brain Sciences
Brain Sciences, Vol 11, Iss 233, p 233 (2021)
Volume 11
Issue 2
Brain Sciences, Vol 11, Iss 233, p 233 (2021)
Volume 11
Issue 2
Noonan syndrome (NS) is a dominant clinically variable and genetically heterogeneous developmental disorder caused by germ-line mutations encoding components of the Ras–MAPK signaling pathway. A few studies have investigated psychopathological feat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49f1e7c6ca4c13ed06548f2ca96bdda5
http://europepmc.org/articles/PMC7918671
http://europepmc.org/articles/PMC7918671
Autor:
Chiara Leoni, Giorgia Piccini, Cristina Caciolo, Francesca Perrino, Stefano Vicari, Patrizio Pasqualetti, Maria Cristina Digilio, Paolo Alfieri, Giuseppe Zampino, Giulia Serra, Marco Tartaglia, Serena Licchelli, Flavia Cirillo
Publikováno v:
European Journal of Paediatric Neurology. 22:170-177
Introduction Noonan syndrome (NS) is an autosomal dominant disorder characterized by short stature, skeletal and haematological/lymphatic defects, distinctive facies, cryptorchidism, and a wide spectrum of congenital heart defects. Recurrent features
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::144ed119818babb0286f209c7e644922
https://doi.org/10.1016/j.ejpn.2017.09.009
https://doi.org/10.1016/j.ejpn.2017.09.009