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Jump to: 2017 | 2016
Number of items: 2.

2017

Ebner, Kathrin, Reintjes, Nadine, Feldkoetter, Markus, Koerber, Friederike, Nagel, Mato, Doetsch, Joeg, Hoppe, Bernd, Weber, Lutz Thorsten, Beck, Bodo B. and Liebau, Max Christoph ORCID: 0000-0003-0494-9080 (2017). A case report on the exceptional coincidence of two inherited renal disorders: ADPKD and Alport syndrome. Clin. Nephrol., 88 (1). S. 45 - 52. DEISENHOFEN-MUENCHEN: DUSTRI-VERLAG DR KARL FEISTLE. ISSN 0301-0430

2016

Riehle, Marc, Buescher, Anja K., Gohlke, Bjoern-Oliver, Kassmann, Mario, Kolatsi-Joannou, Maria, Braesen, Jan H., Nagel, Mato, Becker, Jan U., Winyard, Paul, Hoyer, Peter F., Preissner, Robert, Krautwurst, Dietmar, Gollasch, Maik, Weber, Stefanie and Harteneck, Christian (2016). TRPC6 G757D Loss-of-Function Mutation Associates with FSGS. J. Am. Soc. Nephrol., 27 (9). S. 2771 - 2784. WASHINGTON: AMER SOC NEPHROLOGY. ISSN 1533-3450

This list was generated on Wed Apr 21 03:36:51 2021 CEST.