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Journal of Clinical Medicine Research|March 23, 2013
22q11 deletion syndrome and multiple complex developmental disorder: a case reportValeria Scandurra, Maria R Scordo, Roberto Canitano, et al.
Plos One|February 9, 2017
A comprehensive approach to understand somatic symptoms and their impact on emotional and psychosocial functioning in childrenRita Cerutti, Valentina Spensieri, Carmela Valastro, et al.
Frontiers in Psychiatry|September 26, 2019
Neurodevelopmental Disorders and Adaptive Functions: A Study of Children With Autism Spectrum Disorders (ASD) and/or Attention Deficit and Hyperactivity Disorder (ADHD)Valeria Scandurra, Leonardo Emberti Gialloreti, Francesca Barbanera, et al.
American Journal of Medical Genetics. Part A|March 14, 2007
Clinical and molecular characterization of a patient with a 2q31.2-32.3 deletion identified by array-CGHMaria Antonietta Mencarelli, Rossella Caselli, Chiara Pescucci, et al.
Brain & Development|July 28, 2004
Lymphoblastoid cell lines of Rett syndrome patients exposed to oxidative-stress-induced apoptosisCarla Battisti, Patrizia Formichi, Sergio Antonio Tripodi, et al.
Genes|April 23, 2022
Identification of a Novel SHANK2 Pathogenic Variant in a Patient with a Neurodevelopmental DisorderGabriella Doddato, Alessandra Fabbiani, Valeria Scandurra, et al.
Neuroscience Letters|January 30, 2008
Sympathetic overactivity and plasma leptin levels in Rett syndromeMaurizio Acampa, Francesca Guideri, Jousef Hayek, et al.
International Journal of Molecular Sciences|March 14, 2017
Role of Genetics in the Etiology of Autistic Spectrum Disorder: Towards a Hierarchical Diagnostic StrategyCyrille Robert, Laurent Pasquier, David Cohen, et al.
Early Human Development|August 7, 2015
What do home videos tell us about early motor and socio-communicative behaviours in children with autistic features during the second year of life--An exploratory studyMichele Zappella, Christa Einspieler, Katrin D Bartl-Pokorny, et al.
European Journal of Medical Genetics|November 21, 2020
CDKL5 mutations may mimic Pitt-Hopkins syndrome phenotypeAurora Currò, Gabriella Doddato, Mirella Bruttini, et al.
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