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Boeckhaus, Jan, Hoefele, Julia ORCID: 0000-0002-7917-7129, Riedhammer, Korbinian M., Tonshoff, Burkhard, Ehren, Rasmus, Pape, Lars, Latta, Kay, Fehrenbach, Henry, Lange-Sperandio, Baerbel, Kettwig, Matthias, Hoyer, Peter, Staude, Hagen, Konrad, Martin, John, Ulrike, Gellermann, Jutta, Hoppe, Bernd, Galiano, Matthias, Gessner, Michaela, Pohl, Michael, Bergmann, Carsten, Friede, Tim and Gross, Oliver (2021). Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trial. Clin. Genet., 99 (1). S. 143 - 157. HOBOKEN: WILEY. ISSN 1399-0004
Burgmaier, Kathrin, Brinker, Leonie, Erger, Florian, Beck, Bodo B., Benz, Marcus R., Bergmann, Carsten, Boyer, Olivia, Collard, Laure, Dafinger, Claudia, Fila, Marc, Kowalewska, Claudia, Lange-Sperandio, Baerbel, Massella, Laura, Mastrangelo, Antonio, Mekahli, Djalila, Miklaszewska, Monika, Ortiz-Bruechle, Nadina, Patzer, Ludwig, Prikhodina, Larisa, Ranchin, Bruno, Ranguelov, Nadejda, Schild, Raphael, Seeman, Tomas, Sever, Lale, Sikora, Przemyslaw ORCID: 0000-0002-5698-6863, Szczepanska, Maria ORCID: 0000-0002-6772-1983, Teixeira, Ana, Thumfart, Julia, Uetz, Barbara, Weber, Lutz Thorsten, Wuehl, Elke, Zerres, Klaus, Doetsch, Joerg, Schaefer, Franz and Liebau, Max Christoph ORCID: 0000-0003-0494-9080 (2021). Refining genotype-phenotype correlations in 304 patients with autosomal recessive polycystic kidney disease and PKHD1 gene variants. Kidney Int., 100 (3). S. 650 - 660. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1523-1755
Gross, Oliver, Toenshoff, Burkhard, Weber, Lutz T., Pape, Lars, Latta, Kay, Fehrenbach, Henry, Lange-Sperandio, Baerbel, Zappel, Hildegard, Hoyer, Peter, Staude, Hagen, Koenig, Sabine, John, Ulrike, Gellermann, Jutta, Hoppe, Bernd, Galiano, Matthias, Hoecker, Britta, Ehren, Rasmus, Lerch, Christian, Kashtan, Clifford E., Harden, Markus, Boeckhaus, Jan and Friede, Tim (2020). A multicenter, randomized, placebo -controlled, double-blind phase 3 trial with open -arm comparison indicates safety and ef fi cacy of nephroprotective therapy with ramipril in children with Alport ? s syndrome see commentary. Kidney Int., 97 (6). S. 1275 - 1287. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1523-1755
Kreuzer, Martin, Pruefe, Jenny, Oldhafer, Martina, Bethe, Dirk, Dierks, Marie-Luise, Muether, Silvia, Thumfart, Julia ORCID: 0000-0003-1162-5295, Hoppe, Bernd, Buescher, Anja, Rascher, Wolfgang, Hansen, Matthias, Pohl, Martin, Kemper, Markus J., Drube, Jens, Rieger, Susanne, John, Ulrike, Taylan, Christina, Dittrich, Katalin, Hollenbach, Sabine, Klaus, Guenter, Fehrenbach, Henry, Kranz, Birgitta, Montoya, Carmen, Lange-Sperandio, Baerbel, Ruckenbrodt, Bettina, Billing, Heiko, Staude, Hagen, Heindl-Rusai, Krisztina, Brunkhorst, Reinhard and Pape, Lars ORCID: 0000-0002-3635-6418 (2015). Transitional Care and Adherence of Adolescents and Young Adults After Kidney Transplantation in Germany and Austria A Binational Observatory Census Within the TRANSNephro Trial. Medicine (Baltimore), 94 (48). PHILADELPHIA: LIPPINCOTT WILLIAMS & WILKINS. ISSN 1536-5964
Pruefe, Jenny, Dierks, Marie-Luise, Bethe, Dirk, Oldhafer, Martina, Muether, Silvia, Thumfart, Julia ORCID: 0000-0003-1162-5295, Feldkoetter, Markus, Buescher, Anja, Sauerstein, Katja, Hansen, Matthias, Pohl, Martin, Drube, Jens, Thiel, Florian, Rieger, Susanne, John, Ulrike, Taylan, Christina, Dittrich, Katalin, Hollenbach, Sabine, Klaus, Guenter, Fehrenbach, Henry, Kranz, Birgitta, Montoya, Carmen, Lange-Sperandio, Baerbel, Ruckenbrod, Bettina, Billing, Heiko, Staude, Hagen, Brunkhorst, Reinhard, Rusai, Krisztina, Pape, Lars and Kreuzer, Martin (2017). Transition structures and timing of transfer from paediatric to adult-based care after kidney transplantation in Germany: a qualitative study. BMJ Open, 7 (6). LONDON: BMJ PUBLISHING GROUP. ISSN 2044-6055
Weber, Stefanie, Strasser, Katja, Rath, Sabine, Kittke, Achim, Beicht, Sonja, Alberer, Martin, Lange-Sperandio, Baerbel, Hoyer, Peter F., Benz, Marcus R., Ponsel, Sabine, Weber, Lutz T., Klein, Hanns-Georg and Hoefele, Julia ORCID: 0000-0002-7917-7129 (2016). Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy. Pediatr. Nephrol., 31 (6). S. 941 - 956. NEW YORK: SPRINGER. ISSN 1432-198X