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Issue Date Title Author(s)
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.
3 September 2016 Beta cell function and ongoing autoimmunity in long-standing, childhood onset type 1 diabetes.
Williams, GM; Long, AE; Wilson, IV; et al.
2012 The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy
Urbanek, M; Hayes, MG; Lee, H; et al.
1 May 2010 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
Freathy, RM; Mook-Kanamori, DO; Sovio, U; et al.
3 April 2018 Genetic scores to stratify risk of developing multiple islet autoantibodies and type 1 diabetes: a prospective study in children.
Bonifacio, E; Beyerlein, A; Hippich, M; et al.
15 February 2018 Pharmacogenomics in diabetes: outcomes of thiamine therapy in TRMA syndrome
Habeb, AM; Flanagan, SE; Zulali, MA; et al.
18 June 2019 Association of maternal circulating 25(OH)D and calcium with birth weight: A mendelian randomisation analysis
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