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American Journal of Human Genetics|May 24, 2016
Mutations in SLC26A1 Cause NephrolithiasisHeon Yung Gee, Ikhyun Jun, Daniela A Braun, et al.The Lancet. Healthy Longevity|March 27, 2025
Metformin and physical performance in older people with probable sarcopenia and physical prefrailty or frailty in England (MET-PREVENT): a double-blind, randomised, placebo-controlled trialMiles D Witham, Claire McDonald, Nina Wilson, et al.Journal of the American Society of Nephrology : JASN|December 16, 2017
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1Sven Enerbäck, Daniel Nilsson, Noel Edwards, et al.Plos Genetics|March 8, 2017
Mutations in mitochondrial DNA causing tubulointerstitial kidney diseaseThomas M Connor, Simon Hoer, Andrew Mallett, et al.Conservation Biology : the Journal of the Society for Conservation Biology|October 29, 2025
Mapping area of habitat for inland wetland speciesFrancesca A Ridley, Catherine A Sayer, Louise Mair, et al.Hypertension (Dallas, Tex. : 1979)|July 15, 2024
Progressive Kidney Failure by Angiotensinogen Inactivation in the GermlineFlorian J Wopperer, Eric Olinger, Antje Wiesener, et al.Kidney International|September 12, 2020
Cystinuria: clinical practice recommendationAude Servais, Kay Thomas, Luca Dello Strologo, et al.Human Molecular Genetics|April 25, 2006
In-frame deletion in a novel centrosomal/ciliary protein CEP290/NPHP6 perturbs its interaction with RPGR and results in early-onset retinal degeneration in the rd16 mouseBo Chang, Hemant Khanna, Norman Hawes, et al.Journal of Medical Genetics|January 11, 2015
Evidence of digenic inheritance in Alport syndromeMaria Antonietta Mencarelli, Laurence Heidet, Helen Storey, et al.Plos One|May 18, 2026
Maintaining function and participation through tailored 24-hour movement behaviours for people living with multiple long-term conditions and frailty (The PERSONAL-AGILITY study): Protocol for a randomised controlled feasibility trialMartha Thomas, Louisa Y Herring, Melanie J Davies, et al.Pageof 52