M. R. Caruso

Novel mutations of the CLCN5 gene including a complex allele and A 5′ UTR mutation in Dent disease 1

F. Anglani, L. Peruzzi, N. Glorioso, 2009, Clinical genetics.

Secondary Hyperparathyroidism in Chronic Dialysis Patients: Results of the Italian FARO Survey on Treatment and Mortality

C. Cascone, P. Messa, D. Brancaccio, 2011, Blood Purification.

Diffuse proliferative glomerulonephritis does not determine the worst outcome in childhood-onset lupus nephritis : a 23-year experience in a single centre

S. Giglio, O. Zuffardi, M. R. Caruso, 2009 .

Treatment and long-term outcome in primary distal renal tubular acidosis.

F. Trepiccione, G. Gambaro, Z. Gucev, 2019, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Application of a New Method for GWAS in a Related Case/Control Sample with Known Pedigree Structure: Identification of New Loci for Nephrolithiasis

M. P. Concas, T. Thornton, P. Usai, 2011, PLoS genetics.

Paricalcitol for secondary hyperparathyroidism in renal transplantation.

N. Perico, G. Remuzzi, F. Gaspari, 2015, Journal of the American Society of Nephrology : JASN.

Urinary proteomic analysis in the context of cancer biomarkers

A. Vlahou, H. Mischak, E. Daina, 2022 .

Fresh lemon juice supplementation for the prevention of recurrent stones in calcium oxalate nephrolithiasis: A pragmatic, prospective, randomised, open, blinded endpoint (PROBE) trial

G. Remuzzi, P. Brambilla, M. Trillini, 2021, EClinicalMedicine.

The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis.

E. Mancini, S. Andrulli, L. Garavelli, 2017, Kidney international.

Urinary proteome signature of Renal Cysts and Diabetes syndrome in children

G. Remuzzi, H. Mischak, J. Schanstra, 2019, Scientific Reports.

Primary hyperoxaluria: report of an Italian family with clear sex conditioned penetrance

G. Mandrile, D. Giachino, P. Stratta, 2008, Urological Research.

Medullary sponge kidney associated with primary distal renal tubular acidosis and mutations of the H+-ATPase genes.

M. Genuardi, S. Giglio, O. Zuffardi, 2009, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Urinary proteome signature of Renal Cysts and Diabetes syndrome in children

G. Remuzzi, H. Mischak, J. Schanstra, 2019, Scientific Reports.