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Number of items: 6.

Enerbäck, Sven; Nilsson, Daniel; Edwards, Noel; Heglind, Mikael; Alkanderi, Sumaya; Ashton, Emma; Deeb, Asma; Kokash, Feras E B; Bakhsh, Abdulrahim R A; Van't Hoff, William; Walsh, Stephen B; D'Arco, Felice; Daryadel, Arezoo; Bourgeois, Soline; Wagner, Carsten A; Kleta, Robert; Bockenhauer, Detlef; Sayer, John A (2018). Acidosis and Deafness in Patients with Recessive Mutations in FOXI1. Journal of the American Society of Nephrology (JASN), 29(3):1041-1048.

Aymé, Ségolène; Bockenhauer, Detlef; Day, Simon; Devuyst, Olivier; et al (2017). Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International, 92(4):796-808.

Blanchard, Anne; Bockenhauer, Detlef; Bolignano, Davide; Calò, Lorenzo A; Cosyns, Etienne; Devuyst, Olivier; Ellison, David H; Karet Frankl, Fiona E; Knoers, Nine V.A.M; Konrad, Martin; Lin, Shih-Hua; Vargas-Poussou, Rosa (2017). Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney International, 91(1):24-33.

Klootwijk, Enriko D; Reichold, Markus; Helip-Wooley, Amanda; Tolaymat, Asad; Broeker, Carsten; Robinette, Steven L; Reinders, Joerg; Peindl, Dominika; Renner, Kathrin; Eberhart, Karin; Assmann, Nadine; Oefner, Peter J; Dettmer, Katja; Sterner, Christina; Schroeder, Josef; Zorger, Niels; Witzgall, Ralph; Reinhold, Stephan W; Stanescu, Horia C; Bockenhauer, Detlef; Jaureguiberry, Graciana; Courtneidge, Holly; Hall, Andrew M; Wijeyesekera, Anisha D; Holmes, Elaine; Nicholson, Jeremy K; O'Brien, Kevin; Bernardini, Isa; Krasnewich, Donna M; Arcos-Burgos, Mauricio; Izumi, Yuichiro; Nonoguchi, Hiroshi; Jia, Yuzhi; Reddy, Janardan K; Ilyas, Mohammad; Unwin, Robert J; Gahl, William A; Warth, Richard; Kleta, Robert (2014). Mistargeting of Peroxisomal EHHADH and Inherited Renal Fanconi's Syndrome. New England Journal of Medicine, 370(2):129-138.

Has, Cristina; Spartà, Giuseppina; Kiritsi, Dimitra; Weibel, Lisa; Moeller, Alexander; Vega-Warner, Virginia; Waters, Aoife; He, Yinghong; Anikster, Yair; Esser, Philipp; Straub, Beate K; Hausser, Ingrid; Bockenhauer, Detlef; Dekel, Benjamin; Hildebrandt, Friedhelm; Bruckner-Tuderman, Leena; Laube, Guido F (2012). Integrin α3 mutations with kidney, lung, and skin disease. New England Journal of Medicine, 366(16):1508-1514.

Schoeb, Dominik S; Chernin, Gil; Heeringa, Saskia F; Matejas, Verena; Held, Susanne; Vega-Warner, Virginia; Bockenhauer, Detlef; Vlangos, Christopher N; Moorani, Khemchand N; Neuhaus, Thomas J; Kari, Jameela A; MacDonald, James; Saisawat, Pawaree; Ashraf, Shazia; Ovunc, Bugsu; Zenker, Martin; Hildebrandt, Friedhelm (2010). Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS). Nephrology, Dialysis, Transplantation, 25(9):2970-2976.

This list was generated on Sat May 25 03:05:42 2019 CEST.