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Clinical Journal of the American Society of Nephrology : CJASN|April 24, 2010
Correlation of kidney function, volume and imaging findings, and PKHD1 mutations in 73 patients with autosomal recessive polycystic kidney diseaseMeral Gunay-Aygun, Esperanza Font-Montgomery, Linda Lukose, et al.
Kidney International|September 27, 2008
Characterization of large rearrangements in autosomal dominant polycystic kidney disease and the PKD1/TSC2 contiguous gene syndromeMark B Consugar, Wai C Wong, Patrick A Lundquist, et al.
Contemporary Clinical Trials Communications|April 14, 2021
Improving data quality in observational research studies: Report of the Cure Glomerulonephropathy (CureGN) networkBrenda W Gillespie, Louis-Philippe Laurin, Dawn Zinsser, et al.
Cell|May 13, 2004
Comparative genomics identifies a flagellar and basal body proteome that includes the BBS5 human disease geneJin Billy Li, Jantje M Gerdes, Courtney J Haycraft, et al.
Kidney International|March 23, 2019
Health-related quality of life in glomerular diseasePietro A Canetta, Jonathan P Troost, Shannon Mahoney, et al.
The Journal of Clinical Investigation|September 3, 2024
Increased risk of kidney failure in patients with genetic kidney disordersMark D Elliott, Natalie Vena, Maddalena Marasa, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|November 14, 2018
CureGN Study Rationale, Design, and Methods: Establishing a Large Prospective Observational Study of Glomerular DiseaseLaura H Mariani, Andrew S Bomback, Pietro A Canetta, et al.
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