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Issue Date Title Author(s)
1 August 2013 An in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophy
Weedon, MN; Ellard, S; Prindle, MJ; et al.
18 December 2013 Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study
Oram, RA; Rawlingson, A; Shields, BM; et al.
12 October 2013 The majority of patients with long-duration type 1 diabetes are insulin microsecretors and have functioning beta cells
Oram, RA; Jones, AG; Besser, REJ; et al.
6 September 2017 Costs and Treatment Pathways for Type 2 Diabetes in the UK: A Mastermind Cohort Study
Eibich, P; Green, A; Hattersley, AT; et al.
3 May 2017 Dominant ER Stress-Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts
De Franco, E; Flanagan, SE; Yagi, T; et al.
12 October 2017 Heterozygous RFX6 protein truncating variants are associated with MODY with reduced penetrance
Patel, KA; Kettunen, J; Laakso, M; et al.
17 August 2016 Hypogonadotropic hypogonadism and short stature in patients with diabetes due to neurogenin 3 deficiency
Rubio-Cabezas, O; Luis Gómez, J; Gleisner, A; et al.
2 August 2016 The common p.R114W HNF4A mutation causes a distinct clinical subtype of monogenic diabetes.
Laver, TW; Colclough, K; Shepherd, M; et al.
1 July 2013 The clinical utility of C-peptide measurement in the care of patients with diabetes
Jones, AG; Hattersley, AT
7 February 2017 Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes
Day, JO; Flanagan, SE; Shepherd, MH; et al.