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Canadian Journal of Kidney Health and Disease|December 7, 2020
Complications in Patients With Autosomal Dominant Polycystic Kidney Disease Undergoing Ureteroscopy: A Cohort StudyVinusha Kalatharan, Blayne Welk, Danielle M Nash, et al.
Scientific Reports|December 14, 2023
Real-life use of tolvaptan in ADPKD: a retrospective analysis of a large Canadian cohortLuca Calvaruso, Kevin Yau, Pedram Akbari, et al.
Kidney International|October 28, 2011
A missense mutation in PKD1 attenuates the severity of renal diseaseYork Pei, Zheng Lan, Kairong Wang, et al.
Canadian Journal of Kidney Health and Disease|April 2, 2021
Risk of Hospital Encounters With Kidney Stones in Autosomal Dominant Polycystic Kidney Disease: A Cohort StudyVinusha Kalatharan, Blayne Welk, Danielle M Nash, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|October 14, 2022
Clonal Hematopoiesis of Indeterminate Potential and Kidney Function Decline in the General PopulationBryan Kestenbaum, Alexander G Bick, Caitlyn Vlasschaert, et al.
Frontiers in Genetics|December 6, 2019
Genome-Wide Study Updates in the International Genetics and Translational Research in Transplantation Network (iGeneTRAiN)Claire E Fishman, Maede Mohebnasab, Jessica van Setten, et al.
Kidney International Reports|July 9, 2025
Patients With Mild ADPKD by Kidney Imaging but Low Estimated GFRSeung Heyck Lee, Mauricio Miranda Cam, Taher Dehkharghanian, et al.
BMC Medical Genetics|July 20, 2012
BRCA2 variants and cardiovascular disease in a multi-ethnic studyKevin Zbuk, Changchun Xie, Robin Young, et al.
Clinical Journal of the American Society of Nephrology : CJASN|May 26, 2010
Prospects for mTOR inhibitor use in patients with polycystic kidney disease and hamartomatous diseasesVicente E Torres, Alessandra Boletta, Arlene Chapman, et al.
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