PubMed

Hyperinsulinism-hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype-phenotype correlations.

Kapoor RR, Flanagan SE, Fulton P, Chakrapani A, Chadefaux B, Ben-Omran T, Banerjee I, Shield JP, Ellard S, Hussain K.

Eur J Endocrinol. 2009 Nov;161(5):731-5. Epub 2009 Aug 18.PMID: 19690084 [PubMed - indexed for MEDLINE]Related articlesFree article

3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivity.

Kapoor RR, James C, Flanagan SE, Ellard S, Eaton S, Hussain K.

J Clin Endocrinol Metab. 2009 Jul;94(7):2221-5. Epub 2009 May 5.PMID: 19417036 [PubMed - indexed for MEDLINE]Related articles

Hyperinsulinism in developmental syndromes.

Kapoor RR, James C, Hussain K.

Endocr Dev. 2009;14:95-113. Epub 2009 Feb 27. Review.PMID: 19293578 [PubMed - indexed for MEDLINE]Related articles

The genetic basis of congenital hyperinsulinism.

James C, Kapoor RR, Ismail D, Hussain K.

J Med Genet. 2009 May;46(5):289-99. Epub 2009 Mar 1. Review.PMID: 19254908 [PubMed - indexed for MEDLINE]Related articles

Hyperinsulinaemic hypoglycaemia.

Kapoor RR, Flanagan SE, James C, Shield J, Ellard S, Hussain K.

Arch Dis Child. 2009 Jun;94(6):450-7. Epub 2009 Feb 4. Review.PMID: 19193661 [PubMed - indexed for MEDLINE]Related articles

Diabetes mellitus, exocrine pancreatic deficiency, hypertrichosis, hyperpigmentation, and chronic inflammation: confirmation of a syndrome.

Hussain K, Padidela R, Kapoor RR, James C, Banerjee K, Harper J, Wilson LC, Hennekam RC.

Pediatr Diabetes. 2009 May;10(3):193-7. Epub 2008 Oct 22.PMID: 19175903 [PubMed - indexed for MEDLINE]Related articles

Advances in the diagnosis and management of hyperinsulinemic hypoglycemia.

Kapoor RR, James C, Hussain K.

Nat Clin Pract Endocrinol Metab. 2009 Feb;5(2):101-12. Review. Erratum in: Nat Clin Pract Endocrinol Metab. 2009 Mar;5(3):180. PMID: 19165222 [PubMed - indexed for MEDLINE]Related articles

Congenital hyperinsulinism: [18F]DOPA PET/CT scan of a focal lesion in the head of the pancreas.

Kapoor RR, Gilbert C, Mohnike K, Blankenstein O, Fuechtner F, Hussain K.

Arch Dis Child Fetal Neonatal Ed. 2008 Mar;93(2):F166. No abstract available. PMID: 18296575 [PubMed - indexed for MEDLINE]Related articles

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.

Diabetes. 2008 Jun;57(6):1659-63. Epub 2008 Feb 11.PMID: 18268044 [PubMed - indexed for MEDLINE]Related articlesFree article

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.

Diabetes. 2008 Apr;57(4):1034-42. Epub 2007 Dec 27.PMID: 18162506 [PubMed - indexed for MEDLINE]Related articlesFree article

Monitoring of concordance in growth hormone therapy.

Kapoor RR, Burke SA, Sparrow SE, Hughes IA, Dunger DB, Ong KK, Acerini CL.

Arch Dis Child. 2008 Feb;93(2):147-8. Epub 2007 Sep 3.PMID: 17768149 [PubMed - indexed for MEDLINE]Related articles

Measuring the impact of diagnostic decision support on the quality of clinical decision making: development of a reliable and valid composite score.

Ramnarayan P, Kapoor RR, Coren M, Nanduri V, Tomlinson AL, Taylor PM, Wyatt JC, Britto JF.

J Am Med Inform Assoc. 2003 Nov-Dec;10(6):563-72. Epub 2003 Aug 4.PMID: 12925549 [PubMed - indexed for MEDLINE]Related articlesFree article