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Behavioral Sciences (Basel, Switzerland)|October 26, 2022
Diagnostic and Therapeutic Challenges of Comorbid ASD, ADHD and Psychosis: A Case ReportVeronica Scarselli, Melania Martucci, Maria Novelli, et al.
Clinical Child Psychology and Psychiatry|March 22, 2024
Misdiagnosis of functional neurological symptom disorders in paediatrics: Narrative review and relevant case reportValentina Baglioni, Dario Esposito, Katerina Bernardi, et al.
Frontiers in Neurology|August 25, 2022
Motor, epileptic, and developmental phenotypes in genetic disorders affecting G protein coupled receptors-cAMP signalingSerena Galosi, Luca Pollini, Maria Novelli, et al.
Italian Journal of Pediatrics|December 26, 2022
Early neurodevelopmental outcomes in children with asymptomatic congenital CMV infectionMaria Novelli, Fabio Natale, Anna Di Norcia, et al.
Children (Basel, Switzerland)|February 24, 2024
Comorbidities and Disease Duration in Tourette Syndrome: Impact on Cognition and Quality of Life of ChildrenGiulia Conte, Carola Costanza, Maria Novelli, et al.
Movement Disorders Clinical Practice|July 13, 2024
Autosomal Recessive Guanosine Triphosphate Cyclohydrolase I Deficiency: Redefining the Phenotypic Spectrum and OutcomesMaria Novelli, Manuela Tolve, Vicente Quiroz, et al.
Parkinsonism & Related Disorders|May 4, 2023
GNAO1-related movement disorder: An update on phenomenology, clinical course, and response to treatmentsMaria Novelli, Serena Galosi, Giovanna Zorzi, et al.
Science Signaling|October 28, 2025
Loss of the conserved switch III region in a G protein leads to severe pediatric encephalopathyMikhail Savitsky, Yonika A Larasati, Gonzalo P Solis, et al.
Annals of Neurology|July 1, 2025
The Spectrum of Neurologic Phenotypes Associated With NUS1 Pathogenic Variants: A Comprehensive Case SeriesSarah M Brooker, Maria Novelli, Robert Coukos, et al.
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