15 February 2018 | Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome | Habeb, AM; Flanagan, SE; Zulali, MA; et al. |
17 July 2018 | PLIN1 haploinsufficiency is not associated with lipodystrophy | Laver, TW; Patel, KA; Colclough, K; et al. |
17 September 2018 | ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents | Hattersley, AT; Greeley, SAW; Polak, M; et al. |
3 October 2018 | Homozygosity mapping provides supporting evidence of pathogenicity in recessive Mendelian disease | Wakeling, MN; Laver, TW; Wright, CF; et al. |
4 June 2018 | Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study | Bowman, P; Sulen, Å; Barbetti, F; et al. |
4 June 2018 | Effectiveness and safety of long-term treatment with sulfonylureas in patients with neonatal diabetes due to KCNJ11 mutations: an international cohort study | Bowman, P; Sulen, Å; Barbetti, F; et al. |
30 January 2018 | Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic | Clissold, RL; Fulford, J; Hudson, M; et al. |
12 June 2018 | The Common HNF1A Variant I27L is a Modifier of Age at Diabetes Diagnosis in HNF1A-MODY Individuals. | Locke, JM; Saint-Martin, C; Laver, TW; et al. |
18 September 2018 | A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metformin | Shepherd, MH; Shields, BM; Hudson, M; et al. |