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Human Molecular Genetics|October 23, 2003
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamicsLuca Rampoldi, Gianluca Caridi, Daniela Santon, et al.Journal of the American Society of Nephrology : JASN|April 15, 2005
Familial vesicoureteral reflux: testing replication of linkage in seven new multigenerational kindredsSimone Sanna-Cherchi, Adam Reese, Terry Hensle, et al.Journal of the American Society of Nephrology : JASN|February 9, 2007
Active focal segmental glomerulosclerosis is associated with massive oxidation of plasma albuminLuca Musante, Giovanni Candiano, Andrea Petretto, et al.Pediatric Nephrology (Berlin, Germany)|September 30, 2024
Shiga toxin-producing Escherichia coli infection as a precipitating factor for atypical hemolytic-uremic syndromeGabriele Mortari, Carolina Bigatti, Giulia Proietti Gaffi, et al.Journal of Proteomics|September 16, 2015
Urine proteome analysis in Dent's disease shows high selective changes potentially involved in chronic renal damageLaura Santucci, Giovanni Candiano, Franca Anglani, et al.Journal of the American Society of Nephrology : JASN|December 1, 2001
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosisGianluca Caridi, Roberta Bertelli, Alba Carrea, et al.American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|December 25, 2002
Genetics, clinical and pathological features of glomerulonephritis associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)Gian Marco Ghiggeri, Gianluca Caridi, Umberto Magrini, et al.Journal of Clinical Medicine|August 12, 2022
Multicentric Carpotarsal Osteolysis Syndrome Associated Nephropathy: Novel Variants of MAFB Gene and Literature ReviewStefania Drovandi, Francesca Lugani, Olivia Boyer, et al.Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.Clinical Journal of the American Society of Nephrology : CJASN|July 8, 2011
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotypeMaddalena Gigante, Gianluca Caridi, Eustacchio Montemurno, et al.Pageof 11