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Case Reports in Nephrology|July 31, 2019
Deterioration in Clinical Status Is Not Enough to Suspend Eculizumab: A Genetic Complement-Mediated Atypical Hemolytic Uremic Syndrome Case ReportLuca Calvaruso, Alessandro Naticchia, Pietro Manuel Ferraro, et al.
Kidney & Blood Pressure Research|July 23, 2019
Sodium Fluctuations and Mortality in a General Hospitalized PopulationGianmarco Lombardi, Pietro Manuel Ferraro, Luca Calvaruso, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|December 13, 2019
[ADPKD treatment: Tolvaptan and Octreotide]Marco Galliani, Silvana Chicca, Elio Vitaliano, et al.
Nutrients|August 29, 2024
Potential Add-On Benefits of Dietary Intervention in the Treatment of Autosomal Dominant Polycystic Kidney DiseaseErica Rosati, Giulia Condello, Chiara Tacente, et al.
Scientific Reports|December 14, 2023
Real-life use of tolvaptan in ADPKD: a retrospective analysis of a large Canadian cohortLuca Calvaruso, Kevin Yau, Pedram Akbari, et al.
Clinical Kidney Journal|November 6, 2025
Cardiac complications in autosomal dominant polycystic kidney disease: links to genotype and CKD severityGiulia Condello, Pierluigi Fulignati, Viola D'Ambrosio, et al.
Clinical Biochemistry|September 20, 2015
Utility of serum procalcitonin and C-reactive protein in severity assessment of community-acquired pneumonia in childrenLuisa Agnello, Chiara Bellia, Maria Di Gangi, et al.
Clinical Kidney Journal|September 25, 2025
A novel CT-based radiomics approach for kidney function evaluation in ADPKD: a pilot studyLuca Calvaruso, Pierluigi Fulignati, Luigi Larosa, et al.
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