Skip to content
Log in
Sponsored AI AM CLAUDE, A Beginner's Guide: Learn the basics of working with AI AI AM CLAUDE, A Beginner's Guide: Learn the basics of working with AI

Author

G. Di Rosa

View on Semantic Scholar

4 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Oct 2026

Interpreting Early Neurological Findings in Infants with Gastroesophageal Reflux Symptoms: A Longitudinal Evaluation Using the HINE

Background: Gastroesophageal reflux (GER) is common during infancy. Transient neuromotor features, including alteration in muscle tone, posture, and motor behaviour, have been observed in infants with GER symptoms. Methods: This retrospective observational study included 55 infants with clinical symptoms of GER, includ...

G. Di Rosa, Giulia Spoto, Carla Consoli et al. · 0 citations
Open access Sep 2026

Association Between Toe Walking and Repetitive Behaviors in Children with Autism Spectrum Disorder: A Cross-Sectional Phenotypic Analysis

Background and Objectives: Toe walking (TW) is frequently observed in children with Autism Spectrum Disorder (ASD), yet its clinical significance remains incompletely understood. While previous studies have linked TW to ASD severity and multisystem involvement, its relationship with the behavioral phenotype of repetiti...

M. Gnazzo, G. Bargiacchi, B. Gallai et al. · 0 citations
Open access Aug 2026

Genetic Heterogeneity in Autism Spectrum Disorder: Diagnostic Yield, Recurrent Genes, and Rare Variant-Phenotype Associations from Whole-Exome Sequencing

Overall, this integrative WES study provides clinically actionable diagnoses, highlights recurrent genes, and uncovers phenotype-specific signals, supporting convergent pathways with gene-level heterogeneity.

Zainab Gaouzi, Giulia Spoto, F. Polito et al. · 0 citations
Case report Open access Aug 2026

RFX3 Pathogenic Variants as a Rare Cause of Infantile Epileptic Spasms Syndrome

This case expands the clinical spectrum associated with RFX3 variants, supporting a potential role in IESS and early neurodevelopmental disruption, and highlights the relevance of including RFX3 in the genetic evaluation of patients with IESS and co-occurring neurodevelopmental disorders.

Graziana Ceraolo, Giulia Spoto, M. Trivisano et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.