Showing results (101-110 of 241) with videos related to
Sort By:
Pageof 25
BMJ Open Diabetes Research & Care|May 6, 2026
Acylcarnitines and prediction of renal function decline in type 2 diabetesVincenzo Trischitta, Andrea Fontana, Hetal Shah, et al.Circulation|December 28, 2018
Glycemic Control, Cardiac Autoimmunity, and Long-Term Risk of Cardiovascular Disease in Type 1 Diabetes MellitusGiovane R Sousa, David Pober, Alfonso Galderisi, et al.Pediatric Transplantation|January 24, 2007
Cat-scratch disease relapse in a kidney transplant recipientMichelle N Rheault, Jo-Anne van Burik, Michael Mauer, et al.Journal of Medical Genetics|July 31, 2017
Reduction of podocyte globotriaosylceramide content in adult male patients with Fabry disease with amenable GLA mutations following 6 months of migalastat treatmentMichael Mauer, Alexey Sokolovskiy, Jay A Barth, et al.Diabetes|February 9, 2012
Gene expression differences in skin fibroblasts in identical twins discordant for type 1 diabetesM Luiza Caramori, Youngki Kim, Jason H Moore, et al.Journal of the Renin-Angiotensin-Aldosterone System : JRAAS|October 2, 2007
Angiotensin II receptor blockade blocker pre-treatment largely prevents injury from gradual renal ablation in ratsHye Won Park, Youngki Kim, Kee Hyuck Kim, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|February 21, 2012
Differential expression of laminin isoforms in diabetic nephropathy and other renal diseasesSuman Setty, Alfred A Michael, Alfred J Fish, et al.Journal of Diabetes and Its Complications|November 28, 2012
Normoalbuminuric diabetic kidney disease in the U.S. populationAmy K Mottl, Keun-Sang Kwon, Michael Mauer, et al.Diabetes Care|November 28, 2002
Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effectTomasz Klupa, James H Warram, Anthony Antonellis, et al.Diabetes|July 29, 2003
Genetic modifiers of the age at diagnosis of diabetes (MODY3) in carriers of hepatocyte nuclear factor-1alpha mutations map to chromosomes 5p15, 9q22, and 14q24Sung-Hoon Kim, Xiaowei Ma, Tomasz Klupa, et al.Pageof 25