Flanagan S - Search Results

1

Sirolimus therapy in infants with severe hyperinsulinemic hypoglycemia.

Senniappan S, Alexandrescu S, Tatevian N, Shah P, Arya V, Flanagan S, Ellard S, Rampling D, Ashworth M, Brown RE, Hussain K. Senniappan S, et al. Among authors: flanagan s. N Engl J Med. 2014 Mar 20;370(12):1131-7. doi: 10.1056/NEJMoa1310967. N Engl J Med. 2014. PMID: 24645945 Free article.

2

High-dose glibenclamide can replace insulin therapy despite transitory diarrhea in early-onset diabetes caused by a novel R201L Kir6.2 mutation.

Codner E, Flanagan S, Ellard S, García H, Hattersley AT. Codner E, et al. Among authors: flanagan s. Diabetes Care. 2005 Mar;28(3):758-9. doi: 10.2337/diacare.28.3.758. Diabetes Care. 2005. PMID: 15735229 No abstract available.

3

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 Free article.

4

A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.

Proks P, Arnold AL, Bruining J, Girard C, Flanagan SE, Larkin B, Colclough K, Hattersley AT, Ashcroft FM, Ellard S. Proks P, et al. Among authors: flanagan se. Hum Mol Genet. 2006 Jun 1;15(11):1793-800. doi: 10.1093/hmg/ddl101. Epub 2006 Apr 13. Hum Mol Genet. 2006. PMID: 16613899

5

HLA genotyping supports a nonautoimmune etiology in patients diagnosed with diabetes under the age of 6 months.

Edghill EL, Dix RJ, Flanagan SE, Bingley PJ, Hattersley AT, Ellard S, Gillespie KM. Edghill EL, et al. Among authors: flanagan se. Diabetes. 2006 Jun;55(6):1895-8. doi: 10.2337/db06-0094. Diabetes. 2006. PMID: 16731860

6

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

Pearson ER, Flechtner I, Njølstad PR, Malecki MT, Flanagan SE, Larkin B, Ashcroft FM, Klimes I, Codner E, Iotova V, Slingerland AS, Shield J, Robert JJ, Holst JJ, Clark PM, Ellard S, Søvik O, Polak M, Hattersley AT; Neonatal Diabetes International Collaborative Group. Pearson ER, et al. Among authors: flanagan se. N Engl J Med. 2006 Aug 3;355(5):467-77. doi: 10.1056/NEJMoa061759. N Engl J Med. 2006. PMID: 16885550 Free article.

7

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. Among authors: flanagan se. 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.

8

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. Among authors: flanagan se. 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.

9

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.

10

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. Among authors: flanagan se. 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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