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Glucose intolerance and diabetes are observed in the long-term follow-up of nonpancreatectomized patients with persistent hyperinsulinemic hypoglycemia of infancy due to mutations in the ABCC8 gene.

Gussinyer M, Clemente M, Cebrián R, Yeste D, Albisu M, Carrascosa A.

Diabetes Care. 2008 Jun;31(6):1257-9. Epub 2008 Mar 13.PMID: 18339976 [PubMed - indexed for MEDLINE]Related articlesFree article

Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.

Abdulhadi-Atwan M, Bushman J, Tornovsky-Babaey S, Perry A, Abu-Libdeh A, Glaser B, Shyng SL, Zangen DH.

Diabetes. 2008 Jul;57(7):1935-40. Epub 2008 Apr 4. Erratum in: Diabetes. 2008 Sep;57(9):2552. Bushmann, Jeremy [corrected to Bushman, Jeremy]. PMID: 18390792 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

J Pediatr Endocrinol Metab. 2002 Jul-Aug;15(7):993-1000.PMID: 12199344 [PubMed - indexed for MEDLINE]Related articles

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

Pinney SE, MacMullen C, Becker S, Lin YW, Hanna C, Thornton P, Ganguly A, Shyng SL, Stanley CA.

J Clin Invest. 2008 Aug;118(8):2877-86.PMID: 18596924 [PubMed - indexed for MEDLINE]Related articlesFree article

Protein-sensitive hypoglycemia without leucine sensitivity in hyperinsulinism caused by K(ATP) channel mutations.

Fourtner SH, Stanley CA, Kelly A.

J Pediatr. 2006 Jul;149(1):47-52.PMID: 16860127 [PubMed - indexed for MEDLINE]Related articles

The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.

Sandal T, Laborie LB, Brusgaard K, Eide SA, Christesen HB, Søvik O, Njølstad PR, Molven A.

Clin Genet. 2009 May;75(5):440-8.PMID: 19475716 [PubMed - indexed for MEDLINE]Related articles

The role of ATP sensitive channels in insulin secretion and the implications in persistent hyperinsulinemic hypoglycaemia of infancy (PHHI).

Shah JH, Maguire DJ, Brown D, Cotterill A.

Adv Exp Med Biol. 2007;599:133-8.PMID: 17727257 [PubMed - indexed for MEDLINE]Related articles

A rare mutation in ABCC8/SUR1 leading to altered ATP-sensitive K+ channel activity and beta-cell glucose sensing is associated with type 2 diabetes in adults.

Tarasov AI, Nicolson TJ, Riveline JP, Taneja TK, Baldwin SA, Baldwin JM, Charpentier G, Gautier JF, Froguel P, Vaxillaire M, Rutter GA.

Diabetes. 2008 Jun;57(6):1595-604. Epub 2008 Mar 17.PMID: 18346985 [PubMed - indexed for MEDLINE]Related articlesFree article

A novel mutation associated with congenital hyperinsulinism.

Natarajan G, Aggarwal S, Merritt TA.

Am J Perinatol. 2007 Aug;24(7):401-4. Epub 2007 Jun 27.PMID: 17597441 [PubMed - indexed for MEDLINE]Related articles

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.

Hum Mutat. 2006 Feb;27(2):214.PMID: 16429405 [PubMed - indexed for MEDLINE]Related articles

Persistent hyperinsulinemic hypoglycemia of infancy.

Cohen MM Jr.

Am J Med Genet A. 2003 Nov 1;122A(4):351-3. Review.PMID: 14518075 [PubMed - indexed for MEDLINE]Related articles

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.

Clin Endocrinol (Oxf). 2005 Apr;62(4):458-65.PMID: 15807877 [PubMed - indexed for MEDLINE]Related articles

Mutations in the sulfonylurea receptor gene in relation to the long-term outcome of persistent hyperinsulinemic hypoglycemia of infancy.

Taguchi T, Suita S, Ohkubo K, Ono J.

J Pediatr Surg. 2002 Apr;37(4):593-8.PMID: 11912517 [PubMed - indexed for MEDLINE]Related articles

Understanding protein-sensitive hypoglycemia.

Wolfsdorf JI.

J Pediatr. 2006 Jul;149(1):6-7. No abstract available. PMID: 16860114 [PubMed - indexed for MEDLINE]Related articles

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 [PubMed - indexed for MEDLINE]Related articles

Complex ABCC8 DNA variations in congenital hyperinsulinism: lessons from functional studies.

Muzyamba M, Farzaneh T, Behe P, Thomas A, Christesen HB, Brusgaard K, Hussain K, Tinker A.

Clin Endocrinol (Oxf). 2007 Jul;67(1):115-24. Epub 2007 Apr 27.PMID: 17466004 [PubMed - indexed for MEDLINE]Related articles

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.

Polak M, Dechaume A, Cavé H, Nimri R, Crosnier H, Sulmont V, de Kerdanet M, Scharfmann R, Lebenthal Y, Froguel P, Vaxillaire M; French ND (Neonatal Diabetes) Study Group.

Diabetes. 2008 Apr;57(4):1115-9. Epub 2008 Jan 2.PMID: 18171712 [PubMed - indexed for MEDLINE]Related articlesFree article

Mutations in the ABCC8 (SUR1 subunit of the K(ATP) channel) gene are associated with a variable clinical phenotype.

Klupa T, Kowalska I, Wyka K, Skupien J, Patch AM, Flanagan SE, Noczynska A, Arciszewska M, Ellard S, Hattersley AT, Sieradzki J, Mlynarski W, Malecki MT.

Clin Endocrinol (Oxf). 2009 Sep;71(3):358-62. Epub 2008 Nov 18.PMID: 19021632 [PubMed - indexed for MEDLINE]Related articles

Mutations in the ABCC8 gene can cause autoantibody-negative insulin-dependent diabetes.

Hartemann-Heurtier A, Simon A, Bellanné-Chantelot C, Reynaud R, Cavé H, Polak M, Vaxillaire M, Grimaldi A.

Diabetes Metab. 2009 Jun;35(3):233-5. Epub 2009 Apr 1.PMID: 19342262 [PubMed - indexed for MEDLINE]Related articles

Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism.

Mazor-Aronovitch K, Gillis D, Lobel D, Hirsch HJ, Pinhas-Hamiel O, Modan-Moses D, Glaser B, Landau H.

Eur J Endocrinol. 2007 Oct;157(4):491-7.PMID: 17893264 [PubMed - indexed for MEDLINE]Related articlesFree article