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Diabetes Care|June 25, 2015
Recognition and Management of Individuals With Hyperglycemia Because of a Heterozygous Glucokinase MutationAli J Chakera, Anna M Steele, Anna L Gloyn, et al.
Diabetes|August 8, 2025
Rare Variants in NEUROD1 and PDX1 Are Low-Penetrance Causes of MODY, Whereas Those in APPL1 and WFS1 Are Not Associated With MODYAparajita Sriram, Matthew N Wakeling, Andrew T Hattersley, et al.
Journal of Clinical Research in Pediatric Endocrinology|January 29, 2020
Heterozygous Insulin Receptor (INSR) Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case SeriesAashish Sethi, Nicola Foulds, Sarah Ehtisham, et al.
Journal of Negative Results in Biomedicine|November 28, 2006
A study of association between common variation in the growth hormone-chorionic somatomammotropin hormone gene cluster and adult fasting insulin in a UK Caucasian populationRachel M Freathy, Simon M S Mitchell, Beatrice Knight, et al.
Diabetes Care|November 19, 2015
A Type 1 Diabetes Genetic Risk Score Can Aid Discrimination Between Type 1 and Type 2 Diabetes in Young AdultsRichard A Oram, Kashyap Patel, Anita Hill, et al.
BMJ Open|March 21, 2020
Strategies to identify individuals with monogenic diabetes: results of an economic evaluationJaime L Peters, Rob Anderson, Beverley Shields, et al.
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