Issue 1/2019
Special Issue: The Genetic Aspects of Stone-Formation
Content (13 Articles)
Empirical therapy or precision medicine for kidney stone formers in the ‘-omics’ era?
Giovanni Gambaro
Genetics of common complex kidney stone disease: insights from genome-wide association studies
Runolfur Palsson, Olafur S. Indridason, Vidar O. Edvardsson, Asmundur Oddsson
Calcium-sensing receptor: evidence and hypothesis for its role in nephrolithiasis
Giuseppe Vezzoli, Lorenza Macrina, Giulia Magni, Teresa Arcidiacono
Inherited proximal tubular disorders and nephrolithiasis
Ben Oliveira, Robert Unwin, Stephen B. Walsh
Nephrolithiasis secondary to inherited defects in the thick ascending loop of henle and connecting tubules
Nicolas Faller, Nasser A. Dhayat, Daniel G. Fuster
Cystinuria: genetic aspects, mouse models, and a new approach to therapy
Amrik Sahota, Jay A. Tischfield, David S. Goldfarb, Michael D. Ward, Longqin Hu
Molecular basis of primary hyperoxaluria: clues to innovative treatments
Mirco Dindo, Carolina Conter, Elisa Oppici, Veronica Ceccarelli, Lorella Marinucci, Barbara Cellini
Recent advances in the identification and management of inherited hyperoxalurias
David J. Sas, Peter C. Harris, Dawn S. Milliner
Urinary proteome in inherited nephrolithiasis
Giovanna Capolongo, Miriam Zacchia, Alessandra Perna, Davide Viggiano, Giovambattista Capasso
Living kidney donation from people at risk of nephrolithiasis, with a focus on the genetic forms
Giovanni Gambaro, G. Zaza, F. Citterio, A. Naticchia, P. M. Ferraro