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Biomarkers : Biochemical Indicators of Exposure, Response, and Susceptibility to Chemicals|July 11, 2014
Urinary p-cresol is elevated in young French children with autism spectrum disorder: a replication studyStefano Gabriele, Roberto Sacco, Sonia Cerullo, et al.Scientific Reports|July 26, 2017
Homeostatic Left Heart integration and disintegration links atrio-ventricular covariation's dyshomeostasis in Hypertrophic CardiomyopathyPaolo Piras, Concetta Torromeo, Antonietta Evangelista, et al.Autism Research : Official Journal of the International Society for Autism Research|October 7, 2015
Slow intestinal transit contributes to elevate urinary p-cresol level in Italian autistic childrenStefano Gabriele, Roberto Sacco, Laura Altieri, et al.Journal of Clinical Medicine|May 13, 2026
Growth Outcomes and Relapse Risk in Pediatric Medulloblastoma Survivors with and Without Growth Hormone Therapy: A 23-Year Single-Center Cohort StudyGerdi Tuli, Jessica Munarin, Paola Ragazzi, et al.Antioxidants (Basel, Switzerland)|January 27, 2021
Reevaluation of Serum Arylesterase Activity in Neurodevelopmental DisordersIgnazio Stefano Piras, Stefano Gabriele, Laura Altieri, et al.Scientific Reports|October 8, 2016
Left Atrial trajectory impairment in Hypertrophic Cardiomyopathy disclosed by Geometric Morphometrics and Parallel TransportPaolo Piras, Concetta Torromeo, Federica Re, et al.International Journal of Molecular Sciences|January 26, 2020
<i>NTRK</i> Fusions in Central Nervous System Tumors: A Rare, but Worthy TargetAlessandro Gambella, Rebecca Senetta, Giammarco Collemi, et al.Plos One|April 16, 2015
A new 4D trajectory-based approach unveils abnormal LV revolution dynamics in hypertrophic cardiomyopathyAndrea Madeo, Paolo Piras, Federica Re, et al.Genes, Chromosomes & Cancer|July 2, 2022
Lateralized overgrowth with vascular malformation caused by a somatic PTPN11 pathogenic variant: Another piece added to the puzzle of mosaic RASopathiesAlessandro Mussa, Antonella Turchiano, Simona Cardaropoli, et al.Cancers|December 17, 2024
Molecular and Clinical Features of Adrenocortical Tumors in Beckwith-Wiedemann SpectrumDiana Carli, Federico Rondot, Maria Luca, et al.Pageof 4