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Kidney International|September 3, 2010
The bone and mineral disorder of children undergoing chronic peritoneal dialysisDagmara Borzych, Lesley Rees, Il Soo Ha, et al.
Clinical Journal of the American Society of Nephrology : CJASN|December 1, 2016
Peritoneal Dialysis Access Revision in Children: Causes, Interventions, and OutcomesDagmara Borzych-Duzalka, T Fazil Aki, Marta Azocar, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best PracticeRon T Gansevoort, Mustafa Arici, Thomas Benzing, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 4, 2020
Patient- and parent proxy-reported outcome measures for life participation in children with chronic kidney disease: a systematic reviewJasmijn Kerklaan, Elyssa Hannan, Amanda Baumgart, et al.
Pediatric Nephrology (Berlin, Germany)|July 21, 2014
Demographics of paediatric renal replacement therapy in Europe: a report of the ESPN/ERA-EDTA registryNicholas Chesnaye, Marjolein Bonthuis, Franz Schaefer, et al.
The New England Journal of Medicine|July 16, 2011
MYO1E mutations and childhood familial focal segmental glomerulosclerosisCaterina Mele, Paraskevas Iatropoulos, Roberta Donadelli, et al.
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