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Journal Article
Mueller, Roman-Ulrich, Messchendorp, A. Lianne, Birn, Henrik, Capasso, Giovambattista 
ORCID: 0000-0003-3469-8614, Cornec-Le Gall, Emilie, Devuyst, Olivier ORCID: 0000-0003-3744-4767, van Eerde, Albertien, Guirchoun, Patrick, Harris, Tess, Hoorn, Ewout J., Knoers, Nine V. A. M., Korst, Uwe, Mekahli, Djalila, Le Meur, Yannick, Nijenhuis, Tom, Ong, Albert C. M., Sayer, John A., Schaefer, Franz, Servais, Aude, Tesar, Vladimir, Torra, Roser, Walsh, Stephen B. and Gansevoort, Ron T.
.
An update on the use of tolvaptan for autosomal dominant polycystic kidney disease: consensus statement on behalf of the ERA Working Group on Inherited Kidney Disorders, the European Rare Kidney Disease Reference Network and Polycystic Kidney Disease International.
Nephrol. Dial. Transplant..
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2385
Neirijnck, Yasmine ORCID: 0000-0001-7236-8451, Reginensi, Antoine, Renkema, Kirsten Y., Massa, Filippo, Kozlov, Vladimir M., Dhib, Haroun, Bongers, Ernie M. H. F., Feitz, Wout F., van Eerde, Albertien M. ORCID: 0000-0001-5953-5956, Lefebvre, Veronique, Knoers, Nine V. A. M., Tabatabaei, Mansoureh, Schulz, Herbert, McNeill, Helen ORCID: 0000-0003-1126-5154, Schaefer, Franz, Wegner, Michael, Sock, Elisabeth ORCID: 0000-0001-9925-3136 and Schedl, Andreas ORCID: 0000-0001-9380-7396
(2018).
Sox11 gene disruption causes congenital anomalies of the kidney and urinary tract (CAKUT).
Kidney Int., 93 (5).
S. 1142 - 1154.
NEW YORK:
ELSEVIER SCIENCE INC.
ISSN 1523-1755
Schlingmann, Karl P., Jouret, Francois, Shen, Kuang, Nigam, Anukrati, Arjona, Francisco J., Dafinger, Claudia, Houillier, Pascal, Jones, Deborah P., Kleinerueschkamp, Felix, Oh, Jun, Godefroid, Nathalie, Eltan, Mehmet, Guran, Tulay, Burtey, Stephane, Parotte, Marie-Christine, Koenig, Jens, Braun, Alina, Bos, Caro ORCID: 0000-0001-5016-9435, Serra, Maria Ibars, Rehmann, Holger, Zwartkruis, Fried J. T., Renkema, Kirsten Y., Klingel, Karin, Schulze-Bahr, Eric, Schermer, Bernhard, Bergmann, Carsten, Altmueller, Janine, Thiele, Holger, Beck, Bodo B., Dahan, Karin, Sabatini, David, Liebau, Max C., Vargas-Poussou, Rosa, Knoers, Nine V. A. M., Konrad, Martin and de Baaij, Jeroen H. F.
(2021).
mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.
J. Am. Soc. Nephrol., 32 (11).
S. 2885 - 2900.
WASHINGTON:
AMER SOC NEPHROLOGY.
ISSN 1533-3450