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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2007 | 6 |
2008 | 2 |
2009 | 1 |
2024 | 0 |
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7 results
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Page 1
Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations.
Diabetes Care. 2008 Feb;31(2):204-9. doi: 10.2337/dc07-1785. Epub 2007 Nov 19.
Diabetes Care. 2008.
PMID: 18025408
Free PMC article.
Mutations in ATP-sensitive K+ channel genes cause transient neonatal diabetes and permanent diabetes in childhood or adulthood.
Flanagan SE, Patch AM, Mackay DJ, Edghill EL, Gloyn AL, Robinson D, Shield JP, Temple K, Ellard S, Hattersley AT.
Flanagan SE, et al.
Diabetes. 2007 Jul;56(7):1930-7. doi: 10.2337/db07-0043. Epub 2007 Apr 19.
Diabetes. 2007.
PMID: 17446535
Free PMC article.
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Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.
Edghill EL, Flanagan SE, Patch AM, Boustred C, Parrish A, Shields B, Shepherd MH, Hussain K, Kapoor RR, Malecki M, MacDonald MJ, Støy J, Steiner DF, Philipson LH, Bell GI; Neonatal Diabetes International Collaborative Group; Hattersley AT, Ellard S.
Edghill EL, et al.
Diabetes. 2008 Apr;57(4):1034-42. doi: 10.2337/db07-1405. Epub 2007 Dec 27.
Diabetes. 2008.
PMID: 18162506
Free PMC article.
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An in-frame deletion in Kir6.2 (KCNJ11) causing neonatal diabetes reveals a site of interaction between Kir6.2 and SUR1.
Craig TJ, Shimomura K, Holl RW, Flanagan SE, Ellard S, Ashcroft FM.
Craig TJ, et al.
J Clin Endocrinol Metab. 2009 Jul;94(7):2551-7. doi: 10.1210/jc.2009-0159. Epub 2009 Apr 7.
J Clin Endocrinol Metab. 2009.
PMID: 19351728
Free PMC article.
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Origin of de novo KCNJ11 mutations and risk of neonatal diabetes for subsequent siblings.
Edghill EL, Gloyn AL, Goriely A, Harries LW, Flanagan SE, Rankin J, Hattersley AT, Ellard S.
Edghill EL, et al.
J Clin Endocrinol Metab. 2007 May;92(5):1773-7. doi: 10.1210/jc.2006-2817. Epub 2007 Feb 27.
J Clin Endocrinol Metab. 2007.
PMID: 17327377
Free PMC article.
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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.
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Sulfonylurea treatment in young children with neonatal diabetes: dealing with hyperglycemia, hypoglycemia, and sick days.
Codner E, Flanagan SE, Ugarte F, García H, Vidal T, Ellard S, Hattersley AT.
Codner E, et al.
Diabetes Care. 2007 May;30(5):e28-9. doi: 10.2337/dc06-2134. Epub 2007 Mar 2.
Diabetes Care. 2007.
PMID: 17337505
Free PMC article.
No abstract available.
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