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Arianna Ricciardello

The pediatric psychopharmacology of autism spectrum disorder: A systematic review - Part I: The past and the present
2021 · Antonio M. Persico, Arianna Ricciardello, et al. · Progress in Neuro-Psychopharmacology and Biological Psychiatry · 142
Phenotypic spectrum of NRXN1 mono‐ and bi‐allelic deficiency: A systematic review
2019 · Paola Castronovo, Marco Baccarin, et al. · Clinical Genetics · 63
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The psychopharmacology of autism spectrum disorder and Rett syndrome
2019 · Antonio M. Persico, Arianna Ricciardello, et al. · Handbook of clinical neurology · 54
Genotype–phenotype correlation in Phelan‐McDermid syndrome: A comprehensive review of chromosome 22q13 deleted genes
2021 · Arianna Ricciardello, Pasquale Tomaiuolo, et al. · American Journal of Medical Genetics Part A · 51
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Autism Spectrum Disorder
2022 · Marco O. Bertelli, Muhammad Waqar Azeem, et al. · Springer eBooks · 43
Urinary Untargeted Metabolic Profile Differentiates Children with Autism from Their Unaffected Siblings
2022 · Anna Maria Timperio, Federica Gevi, et al. · Metabolites · 35
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Efficacy and Safety of Q10 Ubiquinol With Vitamins B and E in Neurodevelopmental Disorders: A Retrospective Chart Review
2022 · Francesca Cucinotta, Arianna Ricciardello, et al. · Frontiers in Psychiatry · 24
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Gut mobilization improves behavioral symptoms and modulates urinary p‐cresol in chronically constipated autistic children: A prospective study
2021 · Laura Turriziani, Arianna Ricciardello, et al. · Autism Research · 22
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Evidence that ITGB3 promoter variants increase serotonin blood levels by regulating platelet serotonin transporter trafficking
2018 · Stefano Gabriele, Marco Canali, et al. · Human Molecular Genetics · 19
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Diagnostic yield and clinical impact of chromosomal microarray analysis in autism spectrum disorder
2023 · Francesca Cucinotta, Carla Lintas, et al. · Molecular Genetics & Genomic Medicine · 17
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Cognitive, behavioral and socio-communication skills as predictors of response to Early Start Denver Model: a prospective study in 32 young children with Autism Spectrum Disorder
2024 · Lisa Asta, Tiziana Di Bella, et al. · Frontiers in Psychiatry · 15
Autisms
2020 · Antonio M. Persico, Francesca Cucinotta, et al. · Elsevier eBooks · 15
Clinical, developmental and serotonemia phenotyping of a sample of 70 Italian patients with Phelan-McDermid Syndrome
2024 · Lisa Asta, Arianna Ricciardello, et al. · Journal of Neurodevelopmental Disorders · 14
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Toe walking in children and adolescents with Autism Spectrum Disorder: Relationship with sensory and motor functions,language, cognition, and autism severity
2024 · Michela Camia, Roberto Sacco, et al. · Research in Autism · 13
FARP‐1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family
2020 · Francesca Cucinotta, Arianna Ricciardello, et al. · Molecular Genetics & Genomic Medicine · 12
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Huntingtin gene CAG repeat size affects autism risk: Family‐based and case–control association study
2020 · Ignazio Stefano Piras, Chiara Picinelli, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 8
Depression and Catatonia Associated With Lansoprazole in an Adolescent With Phelan-McDermid Syndrome: A Case Report
2022 · Antonio M. Persico, Arianna Ricciardello, et al. · Journal of Clinical Psychopharmacology · 6
Coenzyme Q10, Vitamin E and Polyvitamin B: an exploratory double-blind randomized cross-over study in Phelan-McDermid Syndrome
2023 · Antonio M. Persico, Arianna Ricciardello, et al. · Rare Disease and Orphan Drugs Journal · 2
Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndrome
2026 · Laura Sandoni, Fethia Chehbani, et al. · Journal of Neurodevelopmental Disorders · 1
Additional file 1 of Chromosome 22q13 terminal deletion size is associated with relevant clinical features in a sample of 63 Italian patients with Phelan-McDermid syndrome
2026 · Laura Sandoni, Fethia Chehbani, et al. · Figshare
Contributors
2020 · Alexej Abyzov, Kevin Cameron Allan, et al. · Elsevier eBooks
Genotype-Phenotype Correlations in Phelan-Mcdermid Syndrome
2019 · Arianna Ricciardello · INSAR 2019 Annual Meeting
Works count: 26
Citation count: 556
H-index: 13
I10-index: 15
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