Flanagan SE - Search Results

1

Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience.

Sharma R, Roy K, Satapathy AK, Kumar A, Nanda PM, Damle N, Houghton JAL, Flanagan SE, Radha V, Mohan V, Jain V. Sharma R, et al. Among authors: flanagan se. Indian Pediatr. 2022 Feb 15;59(2):105-109. doi: 10.1007/s13312-022-2438-0. Epub 2022 Jan 5. Indian Pediatr. 2022. PMID: 34992182 Free PMC article.

2

An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism.

Hussain K, Flanagan SE, Smith VV, Ashworth M, Day M, Pierro A, Ellard S. Hussain K, et al. Among authors: flanagan se. Diabetes. 2008 Jan;57(1):259-63. doi: 10.2337/db07-0998. Epub 2007 Oct 17. Diabetes. 2008. PMID: 17942822

3

Congenital hyperinsulinism due to a compound heterozygous ABCC8 mutation with spontaneous resolution at eight weeks.

Kumaran A, Kapoor RR, Flanagan SE, Ellard S, Hussain K. Kumaran A, et al. Among authors: flanagan se. Horm Res Paediatr. 2010;73(4):287-92. doi: 10.1159/000284394. Epub 2010 Mar 9. Horm Res Paediatr. 2010. PMID: 20215776

4

The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.

Banerjee I, Skae M, Flanagan SE, Rigby L, Patel L, Didi M, Blair J, Ehtisham S, Ellard S, Cosgrove KE, Dunne MJ, Clayton PE. Banerjee I, et al. Among authors: flanagan se. Eur J Endocrinol. 2011 May;164(5):733-40. doi: 10.1530/EJE-10-1136. Epub 2011 Mar 4. Eur J Endocrinol. 2011. PMID: 21378087

5

Congenital hyperinsulinism caused by mutations in ABCC8 (SUR1) gene.

Thakur S, Flanagan SE, Ellard S, Verma IC. Thakur S, et al. Among authors: flanagan se. Indian Pediatr. 2011 Sep;48(9):733-4. Indian Pediatr. 2011. PMID: 21992908

6

The heterogeneity of focal forms of congenital hyperinsulinism.

Ismail D, Kapoor RR, Smith VV, Ashworth M, Blankenstein O, Pierro A, Flanagan SE, Ellard S, Hussain K. Ismail D, et al. Among authors: flanagan se. J Clin Endocrinol Metab. 2012 Jan;97(1):E94-9. doi: 10.1210/jc.2011-1628. Epub 2011 Oct 26. J Clin Endocrinol Metab. 2012. PMID: 22031516 Free PMC article.

7

Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell.

Oçal G, Flanagan SE, Hacihamdioğlu B, Berberoğlu M, Siklar Z, Ellard S, Savas Erdeve S, Okulu E, Akin IM, Atasay B, Arsan S, Yağmurlu A. Oçal G, et al. Among authors: flanagan se. J Pediatr Endocrinol Metab. 2011;24(11-12):1019-23. doi: 10.1515/jpem.2011.347. J Pediatr Endocrinol Metab. 2011. PMID: 22308858

8

SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.

Sansbury FH, Flanagan SE, Houghton JA, Shuixian Shen FL, Al-Senani AM, Habeb AM, Abdullah M, Kariminejad A, Ellard S, Hattersley AT. Sansbury FH, et al. Among authors: flanagan se. Diabetologia. 2012 Sep;55(9):2381-5. doi: 10.1007/s00125-012-2595-0. Epub 2012 Jun 2. Diabetologia. 2012. PMID: 22660720

9

Permanent neonatal diabetes caused by a novel mutation.

Jain V, Flanagan SE, Ellard S. Jain V, et al. Among authors: flanagan se. Indian Pediatr. 2012 Jun;49(6):486-8. doi: 10.1007/s13312-012-0093-6. Indian Pediatr. 2012. PMID: 22796691 Free article.

10

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.

Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K. Kapoor RR, et al. Among authors: flanagan se. Eur J Endocrinol. 2013 Mar 15;168(4):557-64. doi: 10.1530/EJE-12-0673. Print 2013 Apr. Eur J Endocrinol. 2013. PMID: 23345197 Free PMC article.

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