Cited by

• The molecular mechanisms and pharmacotherapy of ATP-sensitive potassium channel gene mutations underlying neonatal diabetes.

  Lang V, Light PE. Lang V, et al. Pharmgenomics Pers Med. 2010;3:145-61. doi: 10.2147/PGPM.S6969. Epub 2010 Nov 24. Pharmgenomics Pers Med. 2010. PMID: 23226049 Free PMC article.
• Mutations in the ABCC8 gene encoding the SUR1 subunit of the KATP channel cause transient neonatal diabetes, permanent neonatal diabetes or permanent diabetes diagnosed outside the neonatal period.

  Patch AM, Flanagan SE, Boustred C, Hattersley AT, Ellard S. Patch AM, et al. Diabetes Obes Metab. 2007 Nov;9 Suppl 2(Suppl 2):28-39. doi: 10.1111/j.1463-1326.2007.00772.x. Diabetes Obes Metab. 2007. PMID: 17919176 Free PMC article.
• Future Roadmaps for Precision Medicine Applied to Diabetes: Rising to the Challenge of Heterogeneity.

  Bowman P, Flanagan SE, Hattersley AT. Bowman P, et al. J Diabetes Res. 2018 Nov 27;2018:3061620. doi: 10.1155/2018/3061620. eCollection 2018. J Diabetes Res. 2018. PMID: 30599002 Free PMC article. Review.
• Sulfonylurea treatment outweighs insulin therapy in short-term metabolic control of patients with permanent neonatal diabetes mellitus due to activating mutations of the KCNJ11 (KIR6.2) gene.

  Tonini G, Bizzarri C, Bonfanti R, Vanelli M, Cerutti F, Faleschini E, Meschi F, Prisco F, Ciacco E, Cappa M, Torelli C, Cauvin V, Tumini S, Iafusco D, Barbetti F; Early-Onset Diabetes Study Group of the Italian Society of Paediatric Endocrinology and Diabetology. Tonini G, et al. Diabetologia. 2006 Sep;49(9):2210-3. doi: 10.1007/s00125-006-0329-x. Epub 2006 Jul 1. Diabetologia. 2006. PMID: 16816952 No abstract available.
• Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.

  Flanagan SE, Edghill EL, Gloyn AL, Ellard S, Hattersley AT. Flanagan SE, et al. Diabetologia. 2006 Jun;49(6):1190-7. doi: 10.1007/s00125-006-0246-z. Epub 2006 Apr 12. Diabetologia. 2006. PMID: 16609879