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Clinical and Investigative Medicine. Medecine Clinique Et Experimentale|November 5, 2003
Molecular genetics of autosomal dominant polycystic kidney diseaseYork PeiClinical Journal of the American Society of Nephrology : CJASN|August 19, 2007
Diagnostic approach in autosomal dominant polycystic kidney diseaseYork PeiNephron. Clinical Practice|November 13, 2010
Practical genetics for autosomal dominant polycystic kidney diseaseYork PeiAdvances in Chronic Kidney Disease|March 12, 2010
Diagnosis and screening of autosomal dominant polycystic kidney diseaseYork Pei, Terry WatnickKidney International|January 26, 2020
Next-generation sequencing for detection of somatic mosaicism in autosomal dominant polycystic kidney diseaseOlivier Devuyst, York PeiSeminars in Nephrology|September 3, 2010
Diagnosis of autosomal-dominant polycystic kidney disease: an integrated approachMoumita Barua, York PeiExpert Opinion on Medical Diagnostics|March 19, 2013
Diagnosis of autosomal dominant polycystic kidney diseaseYork Pei, Xiao ZhaoAdvances in Kidney Disease and Health|December 14, 2023
Assessing the Risk of Progression to Kidney Failure in Patients With Autosomal Dominant Polycystic Kidney DiseaseMatthew B Lanktree, Timothy Kline, York PeiJournal of Nephrology|November 19, 2016
Methodological issues in clinical trials of polycystic kidney disease: a focused reviewIoan-Andrei Iliuta, Abhijat Kitchlu, York PeiEuropean Journal of Pediatrics|April 12, 2011
Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafnessPierre Robitaille, Aicha Merouani, Ning He, et al.Pageof 11