11573/1701266 - 2024 -
Comorbidities and Disease Duration in Tourette Syndrome: Impact on Cognition and Quality of Life of Children Conte, Giulia; Costanza, Carola; Novelli, Maria; Scarselli, Veronica; Arigliani, Elena; Valente, Francesca; Baglioni, Valentina; Terrinoni, Arianna; Chiarotti, Flavia; Cardona, Francesco - 01a Articolo in rivista
rivista: CHILDREN (Basel: MDPI AG, 2014-) pp. - - issn: 2227-9067 - wos: WOS:001169920600001 (0) - scopus: 2-s2.0-85187204195 (0)
11573/1711787 - 2024 -
One-year neurodevelopmental outcome in children with asymptomatic congenital CMV infection Novelli, Maria; Caramuscio, Elvira; Natale, Fabio; Zitarelli, Cristina; Ferri, Rosa; Terrin, Gianluca; Caravale, Barbara - 01a Articolo in rivista
rivista: GLOBAL PEDIATRICS (New York: Elsevier Inc.) pp. - - issn: 2667-0097 - wos: (0) - scopus: (0)
11573/1710607 - 2024 -
“Neurodevelopmental outcome of a child with UPD(16)mat: A case report” Novelli, Maria; Mammarella, Valeria; Calandriello, Francesca; Temofonte, Sara; Goldoni, Marina; Macchiarulo, Ilaria; Versacci, Paolo; Pizzuti, Antonio; Petrilli, Jessica; Brina, Carlo Di; Caravale, Barbara - 01a Articolo in rivista
rivista: GLOBAL PEDIATRICS (New York: Elsevier Inc.) pp. - - issn: 2667-0097 - wos: (0) - scopus: (0)
11573/1711079 - 2023 -
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum Galosi, Serena; Novelli, M; Di Rocco, M; Flex, E; Messina, E; Pollini, Luca; Parrini, E; Pisani, F; Guerrini, Renzo; Leuzzi, V; Martinelli, S - 01f Lettera, Nota
rivista: MOVEMENT DISORDERS (New York, N.Y. : John Wiley & Sons) pp. 2313-2314 - issn: 1531-8257 - wos: WOS:001063564300001 (2) - scopus: 2-s2.0-85168895621 (4)
11573/1706347 - 2023 -
Array-comparative genomic hybridization analysis in a cohort of 130 children with Autism Spectrum Disorders: A single Center Italian Study Martucci, M; Novelli, M; Scarselli, V; Di Palma, F; Fioriello, F; Bernardini, L; Aceti, F; Giacchetti, N; Sogos, C; Pizzuti, A - 01a Articolo in rivista
rivista: LA CLINICA TERAPEUTICA (Roma : Società editrice Universo) pp. - - issn: 1972-6007 - wos: (0) - scopus: (0)
11573/1705193 - 2023 -
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatments Novelli, Maria; Galosi, Serena; Zorzi, Giovanna; Martinelli, Simone; Capuano, Alessandro; Nardecchia, Francesca; Granata, Tiziana; Pollini, Luca; Di Rocco, Martina; Marras, Carlo Efisio; Nardocci, Nardo; Leuzzi, Vincenzo - 01g Articolo di rassegna (Review)
rivista: PARKINSONISM & RELATED DISORDERS (Elsevier Science:Molenwarf 1, 1014 AG Amsterdam The Netherlands:011 31 20 4853597, EMAIL: p.j.bishop@elsevier.com, INTERNET: http://www.elsevier.com, Fax: 011 31 20 4853249) pp. - - issn: 1353-8020 - wos: WOS:001010021100001 (9) - scopus: 2-s2.0-85154532335 (14)
11573/1666784 - 2022 -
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signaling Galosi, Serena; Pollini, Luca; Novelli, Maria; Bernardi, Katerina; Di Rocco, Martina; Martinelli, Simone; Leuzzi, Vincenzo - 01a Articolo in rivista
rivista: FRONTIERS IN NEUROLOGY (Lausanne: Frontiers Research Foundation, 2010-) pp. - - issn: 1664-2295 - wos: WOS:000843322400001 (8) - scopus: 2-s2.0-85136516821 (8)
11573/1663402 - 2022 -
Early neurodevelopmental outcomes in children with asymptomatic congenital CMV infection Novelli, Maria; Natale, Fabio; Di Norcia, Anna; Boiani, Arianna; Temofonte, Sara; Calandriello, Francesca; Zitarelli, Cristina; Caravale, Barbara - 01a Articolo in rivista
rivista: THE ITALIAN JOURNAL OF PEDIATRICS (London : BioMed Central
Ospedaletto : Pacini Editore) pp. 203- - issn: 1824-7288 - wos: WOS:000904070900001 (5) - scopus: 2-s2.0-85144637684 (6)
11573/1666786 - 2022 -
Diagnostic and Therapeutic Challenges of Comorbid ASD, ADHD and Psychosis: A Case Report Scarselli, Veronica; Martucci, Melania; Novelli, Maria; Galosi, Serena; Romani, Maria; Sogos, Carla - 01i Case report
rivista: BEHAVIORAL SCIENCES (Basel : MDPI) pp. - - issn: 2076-328X - wos: WOS:000872178400001 (2) - scopus: 2-s2.0-85140362361 (3)
11573/1541832 - 2021 -
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ10 deficiency in muscle or skin fibroblasts Mero, S.; Salviati, L.; Leuzzi, V.; Rubegni, A.; Calderan, C.; Nardecchia, F.; Galatolo, D.; Desbats, M. A.; Naef, V.; Gemignani, F.; Novelli, M.; Tessa, A.; Battini, R.; Santorelli, F. M.; Marchese, M. - 01a Articolo in rivista
rivista: JOURNAL OF NEUROLOGY (Heidelberg Germany: Springer Verlag) pp. - - issn: 0340-5354 - wos: WOS:000627716700005 (19) - scopus: 2-s2.0-85102491970 (19)