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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.
Clinical Journal of the American Society of Nephrology : CJASN|February 10, 2023
Rapid Progression of Focal Segmental Glomerulosclerosis in Patients with High-Risk APOL1 GenotypesMahmoud Kallash, Yujie Wang, Abigail Smith, et al.
Nature|January 6, 2022
RNA profiles reveal signatures of future health and disease in pregnancyMorten Rasmussen, Mitsu Reddy, Rory Nolan, et al.
Physical Review Letters|December 12, 2001
Antilambda production in Au+Au collisions at 11.7A GeV/cB B Back, R R Betts, J Chang, et al.
Physical Review Letters|April 6, 2001
Baryon rapidity loss in relativistic Au + Au collisionsB B Back, R R Betts, J Chang, 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.
Nature Genetics|November 7, 2006
Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversibleBernward Hinkes, Roger C Wiggins, Rasheed Gbadegesin, et al.
Nature Communications|February 25, 2016
FAT1 mutations cause a glomerulotubular nephropathyHeon Yung Gee, Carolin E Sadowski, Pardeep K Aggarwal, et al.
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