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The Pediatric Infectious Disease Journal|September 28, 2017
Transient Hypothyroidism and Autoimmune Thyroiditis in Children With Chronic Hepatitis C Treated With Pegylated-interferon-α-2b and RibavirinDaniele Serranti, Giuseppe Indolfi, Gabriella Nebbia, et al.
Frontiers in Pediatrics|August 9, 2020
Case Report: Early Treatment With Chenodeoxycholic Acid in Cerebrotendinous Xanthomatosis Presenting as Neonatal CholestasisIrene Degrassi, Chiara Amoruso, Giuseppe Giordano, et al.
World Journal of Gastroenterology|March 7, 2008
Management of cholelithiasis in Italian children: a national multicenter studyClaudia Della Corte, Diego Falchetti, Gabriella Nebbia, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|May 3, 2016
Epilepsy surgery in a liver-transplanted girl with temporal lobe epilepsy and hippocampal sclerosis following PRES with status epilepticusRobertino Dilena, Gabriella Nebbia, Lorenzo Fiorica, et al.
Journal of Hepatology|July 19, 2005
Hepatitis C virus-specific reactivity of CD4+-lymphocytes in children born from HCV-infected womenSilvia Della Bella, Antonio Riva, Elisabetta Tanzi, et al.
Plos One|January 28, 2014
Comparative analysis of rs12979860 SNP of the IFNL3 gene in children with hepatitis C and ethnic matched controls using 1000 Genomes Project dataGiuseppe Indolfi, Giusi Mangone, Elisa Bartolini, et al.
Journal of Hepatology|November 18, 2008
Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patientsRossella Parini, Francesca Furlan, Luigi Notarangelo, et al.
Hepatology (Baltimore, Md.)|February 3, 2022
Sofosbuvir-velpatasvir-voxilaprevir in adolescents 12 to 17 years old with HCV infectionGuiseppe Indolfi, Deirdre Kelly, Gabriella Nebbia, et al.
Orphanet Journal of Rare Diseases|April 5, 2018
KARS-related diseases: progressive leukoencephalopathy with brainstem and spinal cord calcifications as new phenotype and a review of literatureAnna Ardissone, Davide Tonduti, Andrea Legati, et al.
The Journal of Clinical Endocrinology and Metabolism|January 14, 2016
JAG1 Loss-Of-Function Variations as a Novel Predisposing Event in the Pathogenesis of Congenital Thyroid DefectsTiziana de Filippis, Federica Marelli, Gabriella Nebbia, et al.
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