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Autoimmunity Reviews|December 11, 2012
The impact of the profile of biologics on treatment costsGianni Leardini, Chiara RigonAging Clinical and Experimental Research|January 2, 2004
Epidemiology of osteoarthritis: prevalence, risk factors and functional impactMaria Chiara Corti, Chiara RigonEndocrine Connections|August 27, 2025
Optimising diagnosis in children with Short Stature: an integrated clinical and NGS approachLaura Guazzarotti, Chiara Mozzato, Silvia Zoletto, et al.Genes|March 29, 2023
Homozygous <i>TNNI3</i> Mutations and Severe Early Onset Dilated Cardiomyopathy: Patient Report and Review of the LiteratureUgo Sorrentino, Ilaria Gabbiato, Chiara Canciani, et al.Italian Journal of Pediatrics|October 1, 2022
From clinical to molecular diagnosis: relevance of diagnostic strategy in two cases of branchio-oto-renal syndrome - case reportElena Cacciatori, Sebastiano Aleo, Giulietta Scuvera, et al.Seizure|September 7, 2011
Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3AMarilena Vecchi, Matteo Cassina, Alberto Casarin, et al.Audiology Research|October 26, 2021
DFNA20/26 and Other ACTG1-Associated Phenotypes: A Case Report and Review of the LiteratureUgo Sorrentino, Chiara Piccolo, Chiara Rigon, et al.Clinical Chemistry|February 16, 2026
Characterization of STRC Gene Conversions by Nanopore SequencingChiara Rigon, Ugo Sorrentino, Sara Volta, et al.Neuropediatrics|January 8, 2015
Forkhead box G1 gene haploinsufficiency: an emerging cause of dyskinetic encephalopathy of infancyChiara Bertossi, Matteo Cassina, Ambra Cappellari, et al.JIMD Reports|July 26, 2014
A Hunter Patient with a Severe Phenotype Reveals Two Large Deletions and Two Duplications Extending 1.2 Mb Distally to IDS LocusAlessandra Zanetti, Rosella Tomanin, Angelica Rampazzo, et al.Pageof 3