Hussain K - Search Results

1

Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations.

Kapoor RR, Locke J, Colclough K, Wales J, Conn JJ, Hattersley AT, Ellard S, Hussain K. Kapoor RR, et al. Among authors: hussain k. Diabetes. 2008 Jun;57(6):1659-63. doi: 10.2337/db07-1657. Epub 2008 Feb 11. Diabetes. 2008. PMID: 18268044

2

p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.

Kassem SA, Ariel I, Thornton PS, Hussain K, Smith V, Lindley KJ, Aynsley-Green A, Glaser B. Kassem SA, et al. Among authors: hussain k. Diabetes. 2001 Dec;50(12):2763-9. doi: 10.2337/diabetes.50.12.2763. Diabetes. 2001. PMID: 11723059

3

Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.

Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ. Hussain K, et al. J Clin Endocrinol Metab. 2005 Jul;90(7):4376-82. doi: 10.1210/jc.2005-0158. Epub 2005 Apr 5. J Clin Endocrinol Metab. 2005. PMID: 15811927

4

From congenital hyperinsulinism to diabetes mellitus: the role of pancreatic beta-cell KATP channels.

Hussain K, Cosgrove KE. Hussain K, et al. Pediatr Diabetes. 2005 Jun;6(2):103-13. doi: 10.1111/j.1399-543X.2005.00109.x. Pediatr Diabetes. 2005. PMID: 15963039

5

Serum glucagon counterregulatory hormonal response to hypoglycemia is blunted in congenital hyperinsulinism.

Hussain K, Bryan J, Christesen HT, Brusgaard K, Aguilar-Bryan L. Hussain K, et al. Diabetes. 2005 Oct;54(10):2946-51. doi: 10.2337/diabetes.54.10.2946. Diabetes. 2005. PMID: 16186397

6

Costello syndrome and hyperinsulinemic hypoglycemia.

Alexander S, Ramadan D, Alkhayyat H, Al-Sharkawi I, Backer KC, El-Sabban F, Hussain K. Alexander S, et al. Among authors: hussain k. Am J Med Genet A. 2005 Dec 15;139(3):227-30. doi: 10.1002/ajmg.a.31011. Am J Med Genet A. 2005. PMID: 16278907

7

Noninvasive diagnosis of focal hyperinsulinism of infancy with [18F]-DOPA positron emission tomography.

Otonkoski T, Näntö-Salonen K, Seppänen M, Veijola R, Huopio H, Hussain K, Tapanainen P, Eskola O, Parkkola R, Ekström K, Guiot Y, Rahier J, Laakso M, Rintala R, Nuutila P, Minn H. Otonkoski T, et al. Among authors: hussain k. Diabetes. 2006 Jan;55(1):13-8. Diabetes. 2006. PMID: 16380471

8

Mutations in HHEX are not a common cause of monogenic forms of beta cell dysfunction.

Minton JAL, van de Bunt M, Boustred C, Hussain K, Hattersley AT, Ellard S, Gloyn AL. Minton JAL, et al. Among authors: hussain k. Diabetologia. 2007 Sep;50(9):2019-2022. doi: 10.1007/s00125-007-0748-3. Epub 2007 Jul 6. Diabetologia. 2007. PMID: 17618412 No abstract available.

9

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. Diabetes. 2008 Jan;57(1):259-63. doi: 10.2337/db07-0998. Epub 2007 Oct 17. Diabetes. 2008. PMID: 17942822

10

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. Among authors: hussain k. 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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