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Number of items: 4.

Luciani, Alessandro; Sirac, Christophe; Terryn, Sara; Javaugue, Vincent; Prange, Jenny Ann; Bender, Sébastien; Bonaud, Amélie; Cogné, Michel; Aucouturier, Pierre; Ronco, Pierre; Bridoux, Frank; Devuyst, Olivier (2016). Impaired Lysosomal Function Underlies Monoclonal Light Chain-Associated Renal Fanconi Syndrome. Journal of the American Society of Nephrology (JASN), 27(7):2049-2061.

Bakey, Zeineb; Bihoreau, Marie-Thérèse; Piedagnel, Rémi; Delestré, Laure; Arnould, Catherine; de Villiers, Alexandre d'Hotman; Devuyst, Olivier; Hoffmann, Sigrid; Ronco, Pierre; Gauguier, Dominique; Lelongt, Brigitte (2015). The SAM domain of ANKS6 has different interacting partners and mutations can induce different cystic phenotypes. Kidney International, 88(2):299-310.

Mihout, Fabrice; Devuyst, Olivier; Bensman, Albert; Brocheriou, Isabelle; Ridel, Christophe; Wagner, Carsten A; Mohebbi, Nilufar; Boffa, Jean-Jacques; Plaisier, Emmanuelle; Ronco, Pierre (2014). Acute metabolic acidosis in a GLUT2-deficient patient with Fanconi-Bickel syndrome: new pathophysiology insights. Nephrology, Dialysis, Transplantation, 29:iv113-iv116.

Devuyst, Olivier; Antignac, Corinne; Bindels, René J M; Chauveau, Dominique; Emma, Francesco; Gansevoort, Ron; Maxwell, Patrick H; Ong, Albert C M; Remuzzi, Giuseppe; Ronco, Pierre; Schaefer, Franz (2012). The ERA-EDTA Working Group on inherited kidney disorders. Nephrology, Dialysis, Transplantation, 27(1):67-69.

This list was generated on Mon Apr 22 05:41:29 2019 CEST.