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Scientific Reports|May 8, 2024
Development of a clinical calculator to aid the identification of MODY in pediatric patients at the time of diabetes diagnosisBeverley M Shields, Annelie Carlsson, Kashyap Patel, et al.
Pediatric Diabetes|January 8, 2013
Home urine C-peptide creatinine ratio (UCPCR) testing can identify type 2 and MODY in pediatric diabetesRachel E J Besser, Beverley M Shields, Suzanne E Hammersley, et al.
Human Molecular Genetics|November 21, 2023
Penetrance and expressivity of mitochondrial variants in a large clinically unselected populationStuart J Cannon, Timothy Hall, Gareth Hawkes, et al.
Diabetologia|November 10, 2022
The relationship between islet autoantibody status and the genetic risk of type 1 diabetes in adult-onset type 1 diabetesNicholas J Thomas, Helen C Walkey, Akaal Kaur, et al.
The Journal of Clinical Endocrinology and Metabolism|July 19, 2018
PLIN1 Haploinsufficiency Is Not Associated With LipodystrophyThomas W Laver, Kashyap A Patel, Kevin Colclough, et al.
Diabetes|October 27, 2004
Common variants of the hepatocyte nuclear factor-4alpha P2 promoter are associated with type 2 diabetes in the U.K. populationMichael N Weedon, Katharine R Owen, Beverley Shields, et al.
Plos Medicine|October 6, 2006
Combining information from common type 2 diabetes risk polymorphisms improves disease predictionMichael N Weedon, Mark I McCarthy, Graham Hitman, et al.
Ebiomedicine|January 7, 2026
Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetesJames Russ-Silsby, Kevin Colclough, Matthew B Johnson, et al.
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