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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 5, 2021
Clinical characterization of primary hyperoxaluria type 3 in comparison with types 1 and 2Prince Singh, Jason K Viehman, Ramila A Mehta, et al.Applied Clinical Informatics|February 9, 2017
Effect of a Novel Clinical Decision Support Tool on the Efficiency and Accuracy of Treatment Recommendations for Cholesterol ManagementMarianne R Scheitel, Maya E Kessler, Jane L Shellum, et al.Pediatric Nephrology (Berlin, Germany)|March 11, 2019
Prevalence of low molecular weight proteinuria and Dent disease 1 CLCN5 mutations in proteinuric cohortsLada Beara-Lasic, Andrea Cogal, Kristin Mara, et al.Transplantation|April 23, 2009
Kidney transplantation for primary focal segmental glomerulosclerosis: outcomes and response to therapy for recurrenceLatonya J Hickson, Manish Gera, Hatem Amer, et al.Clinical Journal of the American Society of Nephrology : CJASN|March 14, 2020
End Points for Clinical Trials in Primary HyperoxaluriaDawn S Milliner, Tracy L McGregor, Aliza Thompson, et al.Pediatric Transplantation|September 16, 2004
Hand-assisted laparoscopic donor nephrectomy for pediatric kidney allograft recipientsDean Y Kim, Mark D Stegall, Mikel Prieto, et al.Kidney Medicine|April 7, 2022
Kidney Cysts in Hypophosphatemic Rickets With Hypercalciuria: A Case SeriesChristian Hanna, Theodora A Potretzke, Maroun Chedid, et al.American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 10, 2005
Early subclinical coronary artery calcification in young adults who were pediatric kidney transplant recipientsMichael B Ishitani, Dawn S Milliner, Dean Y Kim, et al.Kidney Medicine|November 10, 2025
Natural History of Advanced Primary Hyperoxaluria Type 1: A Retrospective StudyJohn C Lieske, Jaap W Groothoff, Yaacov Frishberg, et al.Clinical Journal of the American Society of Nephrology : CJASN|August 12, 2025
Genetic and Clinical Characterization of a Large Cohort with Suspected Monogenic Stone DiseaseAndrea G Cogal, Ahmed E Ali, Muhammad G Arnous, et al.Pageof 12