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Clinical Kidney Journal|December 25, 2018
Management of autosomal-dominant polycystic kidney disease-state-of-the-artRoman-Ulrich Müller, Thomas BenzingClinical Kidney Journal|February 27, 2018
Enhancing outpatient nephrology experience for internal medicine residentsVarun Agrawal, Kenar D Jhaveri, Hitesh H ShahClinical Kidney Journal|June 6, 2022
Can ketogenic dietary interventions slow disease progression in ADPKD: what we know and what we don'tAlbert C M Ong, Roser TorraClinical Kidney Journal|June 6, 2022
More dissimilarities than affinities between DNAJB11-PKD and ADPKDIsabella Pisani, Marco Allinovi, Viviana Palazzo, et al.Clinical Kidney Journal|June 6, 2022
Ketogenic dietary interventions in autosomal dominant polycystic kidney disease-a retrospective case series study: first insights into feasibility, safety and effectsSebastian Strubl, Simon Oehm, Jacob A Torres, et al.Clinical Kidney Journal|June 6, 2022
An update of proliferative glomerulonephritis with monoclonal immunoglobulin depositsManna Li, Gaosi XuClinical Kidney Journal|June 6, 2022
Management of acute renal replacement therapy in critically ill cirrhotic patientsJimena Del Risco-Zevallos, Alicia Molina Andújar, Gastón Piñeiro, et al.Clinical Kidney Journal|June 6, 2022
New-onset anemia and associated risk of ESKD and death in non-dialysis CKD patients: a multicohort observational studyRoberto Minutolo, Michele Provenzano, Paolo Chiodini, et al.Clinical Kidney Journal|June 6, 2022
Association between bone mineral density at different anatomical sites and both mortality and fracture risk in patients receiving renal replacement therapy: a longitudinal studyDavid A Jaques, Scott Henderson, Andrew DavenportClinical Kidney Journal|May 20, 2022
Treatment of primary hyperoxaluria type 1Asheeta Gupta, Michael J G Somers, Michelle A BaumPageof 300