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Now showing items 31-40 of 87

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Issue DateTitleAuthor(s)
8 June 2012Assessment of endogenous insulin secretion in insulin treated diabetes predicts postprandial glucose and treatment response to prandial insulin Jones, AG; Besser, RE; Shields, BM; et al.
24 March 2017A Low-Frequency Inactivating Akt2 Variant Enriched in the Finnish Population is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk Manning, A; Highland, HM; Gasser, J; et al.
27 December 2019De novo mutations in EIF2B1 affecting eIF2 signaling cause neonatal/early onset diabetes and transient hepatic dysfunction De Franco, E; Caswell, R; Johnson, M; et al.
1 July 2013The clinical utility of C-peptide measurement in the care of patients with diabetes Jones, AG; Hattersley, AT
11 July 2014Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability. Raimondo, A; Chakera, AJ; Thomsen, SK; et al.
1 June 2015Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations. Demirbilek, H; Arya, VB; Ozbek, MN; et al.
14 August 2014Neurogenin 3 is important but not essential for pancreatic islet development in humans. Rubio-Cabezas, O; Codner, E; Flanagan, SE; et al.
6 June 2016Systematic population screening, using biomarkers and genetic testing, identifies 2.5% of the U.K. pediatric diabetes population with monogenic diabetes. Shepherd, M; Shields, B; Hammersley, S; et al.
17 December 2015Adherence to Oral Glucose-Lowering Therapies and Associations With 1-Year HbA1c: A Retrospective Cohort Analysis in a Large Primary Care Database. Farmer, AJ; Rodgers, LR; Lonergan, M; et al.
17 September 2018ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents Hattersley, AT; Greeley, SAW; Polak, M; et al.
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    Hattersley, AT73
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