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Journal Article
Leenen, Esther, Beck, Bodo, Joerres, Achim and Weidemann, Alexander (2020). Rare genetic Diseases with adult onset - Investigations of a Transplant Centre in Cologne. Internist, 61 (SUPPL 1). S. S53 - 1. HEIDELBERG: SPRINGER HEIDELBERG. ISSN 1432-1289
Leenen, Esther, Erger, Florian, Altmuller, Janine 
ORCID: 0000-0003-4372-1521, Wenzel, Andrea, Thiele, Holger, Harth, Ana ORCID: 0000-0002-1551-9214, Tschernoster, Nikolai ORCID: 0000-0002-6058-9342, Lokhande, Shanti, Joerres, Achim, Becker, Jan-Ulrich, Ekici, Arif, Huettel, Bruno, Beck, Bodo and Weidemann, Alexander
(2022).
Alport syndrome and autosomal dominant tubulointerstitial kidney disease frequently underlie end-stage renal disease of unknown origin-a single-center analysis.
Nephrol. Dial. Transplant., 37 (10).
S. 1895 - 1906.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385
Tuschen, Katharina, Anders, Johanna, Elfanish, Amin, Schildgen, Verena, Schildgen, Oliver ORCID: 0000-0003-4297-9627, Becker, Jan Ulrich and Weidemann, Alexander ORCID: 0000-0002-7984-9597
(2021).
Renal transplantation after recovery from COVID-19-a case report with implications for transplant programs in the face of the ongoing corona-pandemic.
BMC Nephrol., 22 (1).
LONDON:
BMC.
ISSN 1471-2369