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Current Opinion in Allergy and Clinical Immunology|November 3, 2005
Cytokine-mediated signalling and early defects in lymphoid developmentSilvia Giliani, Patrizia Mella, Gianfranco Savoldi, et al.Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|November 1, 2016
[Molecular diagnosis of ADPKD]Francesco Scolari, Gianfranco Savoldi, Cinzia Mazza, et al.Current Opinion in Allergy and Clinical Immunology|January 11, 2005
Congenital neutropenia: advances in diagnosis and treatmentRaffaele Badolato, Stefania Fontana, Lucia D Notarangelo, et al.Journal of Clinical Immunology|October 31, 2002
A primary immunodeficiency disorder associated with absence of lymphoid germinal centersEli M Eisenstein, Memet Aker, Gianfranco Savoldi, et al.Pediatric Pulmonology|July 23, 2019
Should isolated Pseudo-Bartter syndrome be considered a CFTR-related disorder of infancy?Piercarlo Poli, Domenico Umberto De Rose, Silviana Timpano, et al.Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|April 13, 2016
[Genetics and genetic counseling]Claudia Izzi, Francesca Liut, Nadia Dallera, et al.Italian Journal of Pediatrics|November 14, 2014
Severe congenital neutropenia due to G6PC3 deficiency: early and delayed phenotype in two patients with two novel mutationsLucia Dora Notarangelo, Gianfranco Savoldi, Sara Cavagnini, et al.Journal of Nephrology|August 6, 2021
Expanding the variability of the ADPKD-GANAB clinical phenotype in a family of Italian ancestryElisa Delbarba, Laura Econimo, Chiara Dordoni, et al.Clinical Kidney Journal|February 26, 2024
Monoallelic pathogenic IFT140 variants are a common cause of autosomal dominant polycystic kidney disease-spectrum phenotypeChiara Dordoni, Letizia Zeni, Diego Toso, et al.Kidney International Reports|December 11, 2020
Variable Expressivity of HNF1B Nephropathy, From Renal Cysts and Diabetes to Medullary Sponge Kidney Through Tubulo-interstitial Kidney DiseaseClaudia Izzi, Chiara Dordoni, Laura Econimo, et al.Pageof 2