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Cancers|December 17, 2024
Molecular and Clinical Features of Adrenocortical Tumors in Beckwith-Wiedemann SpectrumDiana Carli, Federico Rondot, Maria Luca, et al.
The Journal of Pediatrics|June 30, 2024
Molecular Basis and Diagnostic Approach to Isolated and Syndromic Lateralized Overgrowth in ChildhoodSimone Bellucca, Diana Carli, Andrea Gazzin, et al.
Human Genomics|February 14, 2023
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institutionTiziana Vaisitti, Valeria Bracciamà, Angelo Corso Faini, et al.
Genes|November 27, 2025
Functional Characterization of a Novel PBX1 De Novo Missense Variant Identified in a Pediatric Patient with CAKUTCaterina Scolari, Angelo Corso Faini, Giulia Verra, et al.
BMC Psychiatry|August 15, 2013
Effectiveness of lithium in subjects with treatment-resistant depression and suicide risk: a protocol for a randomised, independent, pragmatic, multicentre, parallel-group, superiority clinical trialAndrea Cipriani, Francesca Girlanda, Emilia Agrimi, et al.
European Journal of Endocrinology|April 2, 2024
Functional evaluation of a novel nonsense variant of the calcium-sensing receptor gene leading to hypocalcemiaClaudia Saglia, Francesca Arruga, Caterina Scolari, et al.
Antibiotics (Basel, Switzerland)|December 24, 2021
Efficacy and Safety of Remdesivir over Two Waves of the SARS-CoV-2 PandemicMariacristina Poliseno, Crescenzio Gallo, Donatella Concetta Cibelli, et al.
Cancers|February 11, 2023
Performance Metrics of the Scoring System for the Diagnosis of the Beckwith-Wiedemann Spectrum (BWSp) and Its Correlation with Cancer DevelopmentMaria Luca, Diana Carli, Simona Cardaropoli, et al.
Pediatric Nephrology (Berlin, Germany)|October 9, 2024
Matching clinical and genetic data in pediatric patients at risk of developing cystic kidney diseaseValeria Bracciamà, Tiziana Vaisitti, Fiorenza Mioli, et al.
BMC Medical Genomics|November 28, 2023
Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failureClaudia Saglia, Valeria Bracciamà, Luca Trotta, et al.
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