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Kidney International Reports|December 23, 2017
Tolerability of Aquaretic-Related Symptoms Following Tolvaptan for Autosomal Dominant Polycystic Kidney Disease: Results From TEMPO 3:4Olivier Devuyst, Arlene B Chapman, Susan E Shoaf, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|February 15, 2016
Tolvaptan and Neurocognitive Function in Mild to Moderate Chronic Hyponatremia: A Randomized Trial (INSIGHT)Joseph G Verbalis, Howard Ellison, Mary Hobart, et al.
European Journal of Endocrinology|February 15, 2011
Efficacy and safety of oral tolvaptan therapy in patients with the syndrome of inappropriate antidiuretic hormone secretionJoseph G Verbalis, Suzanne Adler, Robert W Schrier, et al.
The New England Journal of Medicine|November 16, 2006
Tolvaptan, a selective oral vasopressin V2-receptor antagonist, for hyponatremiaRobert W Schrier, Peter Gross, Mihai Gheorghiade, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 22, 2016
Prevalence of autosomal dominant polycystic kidney disease in the European UnionCynthia J Willey, Jaime D Blais, Anthony K Hall, et al.
Clinical Kidney Journal|February 13, 2019
Standardizing total kidney volume measurements for clinical trials of autosomal dominant polycystic kidney diseaseMarie E Edwards, Jaime D Blais, Frank S Czerwiec, et al.
Kidney International Reports|June 11, 2020
A Randomized Trial of Modified-Release Versus Immediate-Release Tolvaptan in ADPKDRonald D Perrone, Arlene B Chapman, Dorothee Oberdhan, et al.
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