Ellard S - Search Results

1

Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two Siblings.

Satapathy AK, Jain V, Ellard S, Flanagan SE. Satapathy AK, et al. Among authors: ellard s. Indian Pediatr. 2016 Oct 8;53(10):912-913. doi: 10.1007/s13312-016-0958-1. Indian Pediatr. 2016. PMID: 27771675 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: ellard 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. Among authors: ellard s. 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: ellard s. 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: ellard s. 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: ellard s. 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

Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers.

Stanik J, Gasperikova D, Paskova M, Barak L, Javorkova J, Jancova E, Ciljakova M, Hlava P, Michalek J, Flanagan SE, Pearson E, Hattersley AT, Ellard S, Klimes I. Stanik J, et al. Among authors: ellard s. J Clin Endocrinol Metab. 2007 Apr;92(4):1276-82. doi: 10.1210/jc.2006-2490. Epub 2007 Jan 9. J Clin Endocrinol Metab. 2007. PMID: 17213273 Free PMC article.

8

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: ellard s. 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.

9

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: ellard s. 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.

10

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. Among authors: ellard s. 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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