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Items: 1 to 20 of 21

1.

Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1.

Huopio H, Reimann F, Ashfield R, Komulainen J, Lenko HL, Rahier J, Vauhkonen I, Kere J, Laakso M, Ashcroft F, Otonkoski T.

J Clin Invest. 2000 Oct;106(7):897-906.

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.

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
4.

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.
6.
7.

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
9.

Diverse roles of K(ATP) channels learned from Kir6.2 genetically engineered mice.

Seino S, Iwanaga T, Nagashima K, Miki T.

Diabetes. 2000 Mar;49(3):311-8. Review.

PMID:
10868950
10.

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
11.

Clinical and genetic heterogeneity in congenital hyperinsulinism.

Meissner T, Mayatepek E.

Eur J Pediatr. 2002 Jan;161(1):6-20. Review.

PMID:
11808881
12.

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.

13.

Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases.

de Lonlay P, Fournet JC, Touati G, Groos MS, Martin D, Sevin C, Delagne V, Mayaud C, Chigot V, Sempoux C, Brusset MC, Laborde K, Bellane-Chantelot C, Vassault A, Rahier J, Junien C, Brunelle F, Nihoul-Fékété C, Saudubray JM, Robert JJ.

Eur J Pediatr. 2002 Jan;161(1):37-48. Review.

PMID:
11808879
14.

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
15.

Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.

Banerjee I, Avatapalle B, Padidela R, Stevens A, Cosgrove KE, Clayton PE, Dunne MJ.

Clin Endocrinol (Oxf). 2013 Jun;78(6):803-13. doi: 10.1111/cen.12153. Review.

PMID:
23347463
16.

Nesidioblastosis unravelled.

Milner RD.

Arch Dis Child. 1996 May;74(5):369-72. Review. No abstract available.

17.

Congenital hyperinsulinism: exclusive human milk and breastfeeding.

Edwards TM, Spatz DL.

Adv Neonatal Care. 2014 Aug;14(4):262-6; quiz 267-8. doi: 10.1097/ANC.0000000000000085. Review.

PMID:
25000103
18.

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.

19.

Rare forms of congenital hyperinsulinism.

Marquard J, Palladino AA, Stanley CA, Mayatepek E, Meissner T.

Semin Pediatr Surg. 2011 Feb;20(1):38-44. doi: 10.1053/j.sempedsurg.2010.10.006. Review.

PMID:
21186003
20.

Congenital hyperinsulinism: global and Japanese perspectives.

Yorifuji T, Masue M, Nishibori H.

Pediatr Int. 2014 Aug;56(4):467-76. doi: 10.1111/ped.12390. Review.

PMID:
24865345

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