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Pediatric Nephrology (Berlin, Germany)|December 12, 2023
Transition of care: lessons from the Standardizing Care to Improve Outcomes in Pediatric End Stage Renal Disease (SCOPE) dialysis collaborativeRaj Munshi, Alison Hewitt Torres, Bertha Ramirez-Preciado, et al.Pediatric Nephrology (Berlin, Germany)|July 2, 2020
Clinical evaluation of the Prismaflex™ HF 20 set and Prismaflex™ system 7.10 for acute continuous kidney replacement therapy (CKRT) in childrenRaj Munshi, Kathy Lee-Son, Richard M Hackbarth, et al.Clinical Journal of the American Society of Nephrology : CJASN|June 25, 2016
Risk Factors for and Outcomes of Catheter-Associated Peritonitis in Children: The SCOPE CollaborativeChristine B Sethna, Kristina Bryant, Raj Munshi, et al.Pediatric Nephrology (Berlin, Germany)|January 10, 2018
Fungal peritonitis in the Standardizing Care to Improve Outcomes in Pediatric End Stage Renal Disease (SCOPE) CollaborativeRaj Munshi, Christine B Sethna, Troy Richardson, et al.Journal of the American Society of Nephrology : JASN|November 13, 2010
MCP-1 gene activation marks acute kidney injuryRaj Munshi, Ali Johnson, Edward D Siew, et al.Clinical Journal of the American Society of Nephrology : CJASN|August 30, 2019
Kidney Support in Children using an Ultrafiltration Device: A Multicenter, Retrospective StudyShina Menon, John Broderick, Raj Munshi, et al.Pediatric Nephrology (Berlin, Germany)|May 9, 2026
Trends in chronic dialysis practices and outcomes in North American children: a 30-year NAPRTCS registry analysisAnkana Daga, Kathleen Altemose, Sarah Twichell, et al.JCI Insight|July 12, 2016
A wearable artificial kidney for patients with end-stage renal diseaseVictor Gura, Matthew B Rivara, Scott Bieber, et al.Pediatric Nephrology (Berlin, Germany)|March 2, 2021
Continued reduction in peritonitis rates in pediatric dialysis centers: results of the Standardizing Care to Improve Outcomes in Pediatric End Stage Renal Disease (SCOPE) CollaborativeAlicia M Neu, Troy Richardson, Heidi Gruhler De Souza, et al.Kidney International|August 5, 2020
An international cohort study of autosomal dominant tubulointerstitial kidney disease due to REN mutations identifies distinct clinical subtypesMartina Živná, Kendrah Kidd, Mohamad Zaidan, et al.Pageof 2