Similar articles for PMID: 15579781

Year	Number of Results
1993	1
1995	1
1996	6
1997	5
1998	8
1999	7
2000	10
2001	8
2002	8
2003	7
2004	10
2005	9
2006	17
2007	26
2008	11
2009	10
2010	11
2011	24
2012	21
2013	14
2014	6
2015	7
2016	6
2017	11
2018	4
2019	7
2020	7
2021	7
2022	6
2023	2
2024	0

1

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.

Tornovsky S, Crane A, Cosgrove KE, Hussain K, Lavie J, Heyman M, Nesher Y, Kuchinski N, Ben-Shushan E, Shatz O, Nahari E, Potikha T, Zangen D, Tenenbaum-Rakover Y, de Vries L, Argente J, Gracia R, Landau H, Eliakim A, Lindley K, Dunne MJ, Aguilar-Bryan L, Glaser B. Tornovsky S, et al. J Clin Endocrinol Metab. 2004 Dec;89(12):6224-34. doi: 10.1210/jc.2004-1233. J Clin Endocrinol Metab. 2004. PMID: 15579781

2

ABCC8 (SUR1) and KCNJ11 (KIR6.2) mutations in persistent hyperinsulinemic hypoglycemia of infancy and evaluation of different therapeutic measures.

Darendeliler F, Fournet JC, Baş F, Junien C, Gross MS, Bundak R, Saka N, Günöz H. Darendeliler F, et al. J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):993-1000. doi: 10.1515/jpem.2002.15.7.993. J Pediatr Endocrinol Metab. 2002. PMID: 12199344

3

Congenital hyperinsulinism associated ABCC8 mutations that cause defective trafficking of ATP-sensitive K+ channels: identification and rescue.

Yan FF, Lin YW, MacMullen C, Ganguly A, Stanley CA, Shyng SL. Yan FF, et al. Diabetes. 2007 Sep;56(9):2339-48. doi: 10.2337/db07-0150. Epub 2007 Jun 15. Diabetes. 2007. PMID: 17575084 Free PMC article.

4

Hyperinsulinism in infancy--genetic aspects.

Darendeliler F, Bas F. Darendeliler F, et al. Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:521-6. Pediatr Endocrinol Rev. 2006. PMID: 17551476 Review.

5

Genotypes of the pancreatic beta-cell K-ATP channel and clinical phenotypes of Japanese patients with persistent hyperinsulinaemic hypoglycaemia of infancy.

Ohkubo K, Nagashima M, Naito Y, Taguchi T, Suita S, Okamoto N, Fujinaga H, Tsumura K, Kikuchi K, Ono J. Ohkubo K, et al. Clin Endocrinol (Oxf). 2005 Apr;62(4):458-65. doi: 10.1111/j.1365-2265.2005.02242.x. Clin Endocrinol (Oxf). 2005. PMID: 15807877

6

Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.

Park SE, Flanagan SE, Hussain K, Ellard S, Shin CH, Yang SW. Park SE, et al. Eur J Endocrinol. 2011 Jun;164(6):919-26. doi: 10.1530/EJE-11-0160. Epub 2011 Mar 21. Eur J Endocrinol. 2011. PMID: 21422196

7

Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI).

Fernández-Marmiesse A, Salas A, Vega A, Fernández-Lorenzo JR, Barreiro J, Carracedo A. Fernández-Marmiesse A, et al. Hum Mutat. 2006 Feb;27(2):214. doi: 10.1002/humu.9401. Hum Mutat. 2006. PMID: 16429405

8

Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.

Gloyn AL, Siddiqui J, Ellard S. Gloyn AL, et al. Hum Mutat. 2006 Mar;27(3):220-31. doi: 10.1002/humu.20292. Hum Mutat. 2006. PMID: 16416420 Review.

9

Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.

Fournet JC, Mayaud C, de Lonlay P, Gross-Morand MS, Verkarre V, Castanet M, Devillers M, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C. Fournet JC, et al. Am J Pathol. 2001 Jun;158(6):2177-84. doi: 10.1016/S0002-9440(10)64689-5. Am J Pathol. 2001. PMID: 11395395 Free PMC article.

10

Genetic analysis of Japanese patients with persistent hyperinsulinemic hypoglycemia of infancy: nucleotide-binding fold-2 mutation impairs cooperative binding of adenine nucleotides to sulfonylurea receptor 1.

Tanizawa Y, Matsuda K, Matsuo M, Ohta Y, Ochi N, Adachi M, Koga M, Mizuno S, Kajita M, Tanaka Y, Tachibana K, Inoue H, Furukawa S, Amachi T, Ueda K, Oka Y. Tanizawa Y, et al. Diabetes. 2000 Jan;49(1):114-20. doi: 10.2337/diabetes.49.1.114. Diabetes. 2000. PMID: 10615958

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