 | Up a level |
2019
Okorn, Christine, Goertz, Anne, Vester, Udo, Beck, Bodo B., Bergmann, Carsten, Habbig, Sandra, Koenig, Jens, Konrad, Martin, Mueller, Dominik, Oh, Jun, Ortiz-Bruechle, Nadina, Patzer, Ludwig, Schild, Raphael, Seeman, Tomas, Staudeu, Hagen, Thumfart, Julia 
ORCID: 0000-0003-1162-5295, Toenshoff, Burkhard, Walden, Ulrike, Weber, Lutz, Zaniew, Marcin, Zappel, Hildegard, Hoyer, Peter F. and Weber, Stefanie
(2019).
HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry.
Pediatr. Nephrol., 34 (6).
S. 1065 - 1076.
NEW YORK:
SPRINGER.
ISSN 1432-198X
2018
Hennies, Imke, Gimpel, Charlotte, Gellermann, Jutta, Moeller, Kristina, Mayer, Brigitte, Dittrich, Katalin, Buescher, Anja K., Hansen, Matthias, Aulbert, Wiebke, Wuehl, Elke, Nissel, Richard, Schalk, Gessa, Weber, Lutz T., Pohl, Michael, Wygoda, Simone, Beetz, Rolf, Klaus, Guenter, Fehrenbach, Henry, Konig, Sabine, Staude, Hagen, Beringer, Ortraud, Bald, Martin, Walden, Ulrike, von Schnakenburg, Christian, Bertram, Gunhard, Wallot, Michael, Haeffner, Karsten, Wiech, Thorsten ORCID: 0000-0003-4053-1474, Hoyer, Peter F. and Pohl, Martin
(2018).
Presentation of pediatric Henoch-Schonlein purpura nephritis changes with age and renal histology depends on biopsy timing.
Pediatr. Nephrol., 33 (2).
S. 277 - 287.
NEW YORK:
SPRINGER.
ISSN 1432-198X
2014
Fehrenbach, Henry, Decker, Christian, Eisenberger, Tobias, Frank, Valeska, Hampel, Tobias, Walden, Ulrike, Amann, Kerstin U., Krueger-Stollfuss, Ingrid, Bolz, Hanno J., Haeffner, Karsten, Pohl, Martin and Bergmann, Carsten (2014). Mutations in WDR19 encoding the intraflagellar transport component IFT144 cause a broad spectrum of ciliopathies. Pediatr. Nephrol., 29 (8). S. 1451 - 1457. NEW YORK: SPRINGER. ISSN 1432-198X