R. Poussou

From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes

R. Salomon, J. Rendu, B. Ranchin, 2011, Human mutation.

A physiological approach to recurrent nephrolithiasis and its genetic determinants

M. Daudon, V. Frochot, E. Letavernier, 2020 .

Fanconi syndrome and severe polyuria: an uncommon clinicobiological presentation of a Gitelman syndrome

R. Salomon, P. Niaudet, A. Garnier, 2014, BMC Pediatrics.

From lowe syndrome to Dent disease: correlations between mutations of the OCRL1 gene and clinical and biochemical phenotypes

R. Salomon, J. Rendu, B. Ranchin, 2011, Human mutation.