Francesco Scibelli
Rome, 00165, Italy
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 11 publications
"BottegaMente": An Italian program of internship for people with autism spectrum disorder.
Journal: Research in developmental disabilities
Published: April 24, 2024
Characterizing individual differences in children and adolescents with autism spectrum disorder: a descriptive study.
Journal: Frontiers in psychology
Published: October 18, 2023
Differences and Similarities in Adaptive Functioning between Children with Autism Spectrum Disorder and Williams-Beuren Syndrome: A Longitudinal Study.
Journal: Genes
Published: June 06, 2022
A Comparison of Adaptive Functioning Between Children With Duplication 7 Syndrome and Williams-Beuren Syndrome: A Pilot Investigation.
Journal: Frontiers in psychiatry
Published: January 27, 2022
Cooperative Parent-Mediated Therapy in Children with Fragile X Syndrome and Williams Beuren Syndrome: A Pilot RCT Study of a Transdiagnostic Intervention-Preliminary Data.
Journal: Brain sciences
Published: October 12, 2021
Manic and Depressive Symptoms in Children Diagnosed with Noonan Syndrome.
Journal: Brain sciences
Published: December 24, 2020
Clinical and individual features associated with maternal stress in young adolescents with autism spectrum disorder.
Journal: Autism research : official journal of the International Society for Autism Research
Published: November 26, 2020
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling.
Journal: Brain sciences
Published: September 24, 2020
Comparison of Adaptive Functioning in Children with Williams Beuren Syndrome and Autism Spectrum Disorder: A Cross-Syndrome Study.
Journal: Autism research : official journal of the International Society for Autism Research
Published: June 04, 2020
TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics.
Journal: International journal of molecular sciences
Published: January 31, 2020
Further insight into the neurobehavioral pattern of children carrying the 2p16.3 heterozygous deletion involving NRXN1: Report of five new cases.
Journal: Genes, brain, and behavior
Published: December 13, 2019
Showing 1-11 of 11
Last Updated: 09/26/2026