31 March 2016 | Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes | Babiker, T; Vedovato, N; Patel, K; et al. |
9 June 2016 | Isolated pancreatic aplasia due to a hypomorphic PTF1A mutation | Houghton, JA; Swift, GH; Shaw-Smith, C; et al. |
27 April 2016 | Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk. | Vedovato, N; Cliff, E; Proks, P; et al. |
1 November 2016 | Low IgE is a useful tool to identify STAT3 gain-of-functionmMutations. | Johnson, MB; Flanagan, SE; Martins, TB; et al. |
1 September 2016 | Prematurity should not prevent genetic testing for neonatal diabetes | Besser, RE; Flanagan, SE; Mackay, DG; et al. |
1 October 2016 | Monogenic autoimmune diseases of the endocrine system | Johnson, MB; Hattersley, AT; Flanagan, SE |
5 April 2016 | Type 1 Diabetes Genetic Risk Score: a novel tool to discriminate monogenic and type 1 diabetes | Patel, KA; Oram, RA; Flanagan, SE; et al. |
11 April 2016 | Psychiatric morbidity in children with KCNJ11 neonatal diabetes | Bowman, P; Broadbridge, E; Knight, BA; et al. |