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Autism Research : Official Journal of the International Society for Autism Research|November 23, 2021
Gut mobilization improves behavioral symptoms and modulates urinary p-cresol in chronically constipated autistic children: A prospective studyLaura Turriziani, Arianna Ricciardello, Francesca Cucinotta, et al.
Journal of Clinical Medicine|September 23, 2022
Impact of Three Kinds of Early Interventions on Developmental Profile in Toddlers with Autism Spectrum DisorderFrancesca Cucinotta, Luigi Vetri, Liliana Ruta, et al.
Journal of Cardiovascular Medicine (Hagerstown, Md.)|July 9, 2020
Arrhythmic event prediction in patients with heart failure and reduced ejection fractionGloria Santangelo, Francesca Bursi, Maria S Negroni, et al.
Molecular Genetics & Genomic Medicine|May 15, 2023
Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorderFrancesca Cucinotta, Carla Lintas, Pasquale Tomaiuolo, et al.
Brain Sciences|October 23, 2021
Role of COMT V158M Polymorphism in the Development of Dystonia after Administration of Antipsychotic DrugsAntonio Gennaro Nicotera, Gabriella Di Rosa, Laura Turriziani, et al.
Journal of Neurodevelopmental Disorders|October 4, 2024
Clinical, developmental and serotonemia phenotyping of a sample of 70 Italian patients with Phelan-McDermid SyndromeLisa Asta, Arianna Ricciardello, Francesca Cucinotta, et al.
Frontiers in Psychiatry|November 3, 2025
Donkey-assisted therapy in mental health conditions: a systematic reviewAlessia Fulgenzi, Antonio Raffa, Carmela De Domenico, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 12, 2020
Huntingtin gene CAG repeat size affects autism risk: Family-based and case-control association studyIgnazio Stefano Piras, Chiara Picinelli, Raffaele Iennaco, et al.
Journal of Neurodevelopmental Disorders|May 27, 2026
Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndromeLaura Sandoni, Fethia Chehbani, Lisa Asta, et al.
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