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Displaying 7 results.
    • Journal article
    Albuminuria and tolvaptan in autosomal-dominant polycystic kidney disease: results of the TEMPO 3:4 Trial.
    Gansevoort, Ron T Meijer, Esther Chapman, Arlene B Czerwiec, Frank S Devuyst, Olivier[UCL] Grantham, Jared J Higashihara, Eiji Krasa, Holly B Ouyang, John Perrone, Ronald D Torres, Vicente E TEMPO 3:4 Investigators (2016) Nephrology, Dialysis, Transplantation — Vol. 31, no. 11, p. 1887-1894 (2016)
    • Journal article
    Rationale and design of the TEMPO (Tolvaptan Efficacy and Safety in Management of Autosomal Dominant Polycystic Kidney Disease and its Outcomes) 3-4 Study.
    Torres, Vicente E. Meijer, Esther Bae, Kyongtae T. Chapman, Arlene B. Devuyst, Olivier[UCL] Gansevoort, Ron T. Grantham, Jared J. Higashihara, Eiji Perrone, Ronald D. Krasa, Holly B. Ouyang, John J. Czerwiec, Frank S. (2011) American Journal of Kidney Diseases — Vol. 57, no. 5, p. 692-699 (2011)
    • Journal article
    Flank pain has a significant adverse impact on quality of life in ADPKD: the CYSTic-QoL study
    Winterbottom, Jean Simms, Roslyn J Caroli, Anna Cornec-Le Gall, Emilie Demoulin, Nathalie[UCL] Furlano, Monica Meijer, Esther Devuyst, Olivier[UCL] Gansevoort, Ron T Le-Meur, Yannick Perico, Norberto Torra, Roser Ong, Albert C M (2022) Clinical kidney journal — Vol. 15, no. 11, p. 2063-2071 (2022)
    • Journal article
    HYDROchlorothiazide versus placebo to PROTECT polycystic kidney disease patients and improve their quality of life: study protocol and rationale for the HYDRO-PROTECT randomized controlled trial.
    Bais, Thomas Meijer, Esther Kramers, Bart J Vart, Priya Vervloet, Marc Salih, Mahdi Bammens, Bert Demoulin, Nathalie[UCL] Todorova, Polina Müller, Roman-Ulrich Halbritter, Jan Paliege, Alexander Gall, Emilie Cornec-Le Knebelmann, Bertrand Torra, Roser Ong, Albert C M Karet Frankl, Fiona E Gansevoort, Ron T (2024) Trials — Vol. 25, no.1, p. 120 (2024)
    • Journal article
    Analysis of data from the ERA-EDTA Registry indicates that conventional treatments for chronic kidney disease do not reduce the need for renal replacement therapy in autosomal dominant polycystic kidney disease
    Spithoven, Edwin M Kramer, Anneke Meijer, Esther Orskov, Bjarne Wanner, Christoph Caskey, Fergus Collart, Frederic Finne, Patrik Fogarty, Damian G Groothoff, Jaap W Hoitsma, Andries Nogier, Marie-Béatrice Postorino, Maurizio Ravani, Pietro Zurriaga, Oscar Jager, Kitty J Gansevoort, Ron T ERA-EDTA Registry EuroCYST Consortium WGIKD Devuyst, Olivier[UCL] Pirson, Yves[UCL] (2014) Kidney International — Vol. 86, no. 6, p. 1244-1252 (2014)
    • Journal article
    Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival--an analysis of data from the ERA-EDTA Registry.
    Spithoven, Edwin M Kramer, Anneke Meijer, Esther Orskov, Bjarne Wanner, Christoph Abad, Jose M Aresté, Nuria de la Torre, Ramón Alonso Caskey, Fergus Couchoud, Cécile Finne, Patrik Heaf, James Hoitsma, Andries de Meester, Johan Pascual, Julio Postorino, Maurizio Ravani, Pietro Zurriaga, Oscar Jager, Kitty J Gansevoort, Ron T Devuyst, Olivier[UCL] Pirson, Yves[UCL] EuroCYST Consortiu WGIKD ERA-EDTA Registry (2014) Nephrology, Dialysis, Transplantation — Vol. 29, no.suppl 4, p. iv15-iv25 (2014)
    • Journal article
    Monoallelic IFT140 pathogenic variants are an important cause of the autosomal dominant polycystic kidney-spectrum phenotype.
    Senum, Sarah R Li, Ying Sabrina M Benson, Katherine A Joli, Giancarlo Olinger, Eric[UCL] Lavu, Sravanthi Madsen, Charles D Gregory, Adriana V Neatu, Ruxandra Kline, Timothy L Audrézet, Marie-Pierre Outeda, Patricia Nau, Cherie B Meijer, Esther Ali, Hamad Steinman, Theodore I Mrug, Michal Phelan, Paul J Watnick, Terry J Peters, Dorien J M Ong, Albert C M Conlon, Peter J Perrone, Ronald D Cornec-Le Gall, Emilie Hogan, Marie C Torres, Vicente E Sayer, John A Genomics England Research Consortium, the HALT PKD, CRISP, DIPAK, ADPKD Modifier, and TAME PKD studies Harris, Peter C (2022) American journal of human genetics — Vol. 109, no.1, p. 136-156 (2022)