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Items: 1 to 20 of 28

1.

Genotype-phenotype correlations in children with congenital hyperinsulinism due to recessive mutations of the adenosine triphosphate-sensitive potassium channel genes.

Henwood MJ, Kelly A, Macmullen C, Bhatia P, Ganguly A, Thornton PS, Stanley CA.

J Clin Endocrinol Metab. 2005 Feb;90(2):789-94. Epub 2004 Nov 23.

PMID:
15562009
2.

[Congenital hyperinsulinism in newborn and infant].

Giurgea I, Ribeiro MJ, Boddaert N, Touati G, Robert JJ, Saudubray JM, Jaubert F, Bellanné-Chantelot C, Brunelle F, Nihoul-Fékété C, de Lonlay P.

Arch Pediatr. 2005 Nov;12(11):1628-35. Epub 2005 Sep 28. Review. French.

PMID:
16198094
3.

Congenital hyperinsulinism: molecular basis of a heterogeneous disease.

Meissner T, Beinbrech B, Mayatepek E.

Hum Mutat. 1999;13(5):351-61. Review.

PMID:
10338089
5.

The structure and function of the ATP-sensitive K+ channel in insulin-secreting pancreatic beta-cells.

Miki T, Nagashima K, Seino S.

J Mol Endocrinol. 1999 Apr;22(2):113-23. Review.

PMID:
10194514
6.

Molecular biology of adenosine triphosphate-sensitive potassium channels.

Aguilar-Bryan L, Bryan J.

Endocr Rev. 1999 Apr;20(2):101-35. Review.

PMID:
10204114
7.

KATP channel mutations in congenital hyperinsulinism.

Saint-Martin C, Arnoux JB, de Lonlay P, Bellanné-Chantelot C.

Semin Pediatr Surg. 2011 Feb;20(1):18-22. doi: 10.1053/j.sempedsurg.2010.10.012. Review.

PMID:
21185999
8.
9.

Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.

Sharma N, Crane A, Gonzalez G, Bryan J, Aguilar-Bryan L.

Kidney Int. 2000 Mar;57(3):803-8. Review.

10.

A view of sur/KIR6.X, KATP channels.

Babenko AP, Aguilar-Bryan L, Bryan J.

Annu Rev Physiol. 1998;60:667-87. Review.

PMID:
9558481
11.

Hyperinsulinism in infancy--genetic aspects.

Darendeliler F, Bas F.

Pediatr Endocrinol Rev. 2006 Aug;3 Suppl 3:521-6. Review. Erratum in: Pediatr Endocrinol Rev. 2007 Sep;5(1):470.

PMID:
17551476
12.

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.

Flanagan SE, Clauin S, Bellanné-Chantelot C, de Lonlay P, Harries LW, Gloyn AL, Ellard S.

Hum Mutat. 2009 Feb;30(2):170-80. doi: 10.1002/humu.20838. Review.

PMID:
18767144
13.

Molecular mechanisms of neonatal hyperinsulinism.

Giurgea I, Bellanné-Chantelot C, Ribeiro M, Hubert L, Sempoux C, Robert JJ, Blankenstein O, Hussain K, Brunelle F, Nihoul-Fékété C, Rahier J, Jaubert F, de Lonlay P.

Horm Res. 2006;66(6):289-96. Epub 2006 Sep 26. Review.

PMID:
17003566
14.
15.

ATP-sensitive potassium channelopathies: focus on insulin secretion.

Ashcroft FM.

J Clin Invest. 2005 Aug;115(8):2047-58. Review.

16.

Human K(ATP) channelopathies: diseases of metabolic homeostasis.

Olson TM, Terzic A.

Pflugers Arch. 2010 Jul;460(2):295-306. doi: 10.1007/s00424-009-0771-y. Epub 2009 Dec 24. Review.

17.

Molecular biology of K(ATP) channels and implications for health and disease.

Akrouh A, Halcomb SE, Nichols CG, Sala-Rabanal M.

IUBMB Life. 2009 Oct;61(10):971-8. doi: 10.1002/iub.246. Review.

18.

ATP-sensitive potassium channels in health and disease.

Clark R, Proks P.

Adv Exp Med Biol. 2010;654:165-92. doi: 10.1007/978-90-481-3271-3_8. Review.

19.

Genetics of neonatal hyperinsulinism.

Glaser B, Thornton P, Otonkoski T, Junien C.

Arch Dis Child Fetal Neonatal Ed. 2000 Mar;82(2):F79-86. Review.

20.

Trafficking of ATP-sensitive potassium channels in health and disease.

Sivaprasadarao A, Taneja TK, Mankouri J, Smith AJ.

Biochem Soc Trans. 2007 Nov;35(Pt 5):1055-9. Review.

PMID:
17956278

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