SIX2 and BMP4 Mutations Associate With Anomalous Kidney Development by WEBER, Stefanie, TAYLOR, Jaclyn C, EMRE, Sevinc, MARCO GHIGGERI, Gian, BAKKALOGLU, Aysin, MEHLS, Otto, ANTIGNAC, Corinne, NETWORK, Escape, SCHAEFER, Franz, BURDINE, Rebecca D, WINYARD, Paul, BAKER, Kari F, SULLIVAN-BROWN, Jessica, SCHILD, Raphael, KNUPPEL, Tanja, ZUROWSKA, Aleksandra M, CALDAS-ALFONSO, Alberto, LITWIN, Mieczyslaw

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Recurrence of proteinuria 10 years post-transplant in NPHS2-associated focal segmental glomerulosclerosis after conversion from cyclosporin A to sirolimus by Höcker, Britta, Knüppel, Tanja, Waldherr, Rüdiger, Schaefer, Franz, Weber, Stefanie, Tönshoff, Burkhard

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Clinical course and NPHS2 analysis in patients with late steroid-resistant nephrotic syndrome by Schwaderer, Peter, Knüppel, Tanja, Konrad, Martin, Mehls, Otto, Schärer, Karl, Schaefer, Franz, Weber, Stefanie

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Prevalence of mutations in renal developmental genes in children with renal hypodysplasia : Results of the ESCAPE study by WEBER, Stefanie, MORINIERE, Vincent, WÜHL, Elke, ZUROWSKA, Aleksandra M, MEHLS, Otto, ANTIGNAC, Corinne, SCHAEFER, Franz, SALOMON, Remi, KNÜPPEL, Tanja, CHARBIT, Marina, DUSEK, Jiri, GHIGGERI, Gian Marco, JANKAUSKIENE, Augustina, MIR, Sevgi, MONTINI, Giovanni, PECO-ANTIC, Amira

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Double homozygous missense mutations in DACH1 and BMP4 in a patient with bilateral cystic renal dysplasia by Schild, Raphael, Knüppel, Tanja, Konrad, Martin, Bergmann, Carsten, Trautmann, Agnes, Kemper, Markus J, Wu, Kongming, Yaklichkin, Sergey, Wang, Jing, Pestell, Richard, Müller-Wiefel, Dirk E, Schaefer, Franz, Weber, Stefanie

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DEAP-HUS: Deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome by Zipfel, Peter F., Mache, Christoph, Müller, Dominik, Licht, Christoph, Wigger, Marianne, Skerka, Christine

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