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Items: 1 to 20 of 98

1.

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
2.

Mutational analysis of ABCC8, KCNJ11, GLUD1, HNF4A and GCK genes in 30 Chinese patients with congenital hyperinsulinism.

Sang Y, Xu Z, Liu M, Yan J, Wu Y, Zhu C, Ni G.

Endocr J. 2014;61(9):901-10. Epub 2014 Jul 8.

3.

Genetics of congenital hyperinsulinemic hypoglycemia.

Flanagan SE, Kapoor RR, Hussain K.

Semin Pediatr Surg. 2011 Feb;20(1):13-7. doi: 10.1053/j.sempedsurg.2010.10.004. Review.

PMID:
21185998
4.

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism.

Snider KE, Becker S, Boyajian L, Shyng SL, MacMullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A.

J Clin Endocrinol Metab. 2013 Feb;98(2):E355-63. doi: 10.1210/jc.2012-2169. Epub 2012 Dec 28.

5.

Congenital hyperinsulinism due to mutations in HNF4A and HADH.

Kapoor RR, Heslegrave A, Hussain K.

Rev Endocr Metab Disord. 2010 Sep;11(3):185-91. doi: 10.1007/s11154-010-9148-y. Review.

PMID:
20931292
6.

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.

Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K.

Eur J Endocrinol. 2013 Mar 15;168(4):557-64. doi: 10.1530/EJE-12-0673. Print 2013 Apr.

7.

Congenital hyperinsulinism: clinical and molecular analysis of a large Italian cohort.

Faletra F, Athanasakis E, Morgan A, Biarnés X, Fornasier F, Parini R, Furlan F, Boiani A, Maiorana A, Dionisi-Vici C, Giordano L, Burlina A, Ventura A, Gasparini P.

Gene. 2013 May 25;521(1):160-5. doi: 10.1016/j.gene.2013.03.021. Epub 2013 Mar 16.

PMID:
23506826
8.

Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations.

Flanagan SE, Kapoor RR, Mali G, Cody D, Murphy N, Schwahn B, Siahanidou T, Banerjee I, Akcay T, Rubio-Cabezas O, Shield JP, Hussain K, Ellard S.

Eur J Endocrinol. 2010 May;162(5):987-92. doi: 10.1530/EJE-09-0861. Epub 2010 Feb 17.

9.

The genetic basis of congenital hyperinsulinism.

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

J Med Genet. 2009 May;46(5):289-99. doi: 10.1136/jmg.2008.064337. Epub 2009 Mar 1. Review.

PMID:
19254908
10.

Insights in congenital hyperinsulinism.

Hussain K.

Endocr Dev. 2007;11:106-21. Review.

PMID:
17986831
11.

High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.

Rozenkova K, Malikova J, Nessa A, Dusatkova L, Bjørkhaug L, Obermannova B, Dusatkova P, Kytnarova J, Aukrust I, Najmi LA, Rypackova B, Sumnik Z, Lebl J, Njølstad PR, Hussain K, Pruhova S.

J Clin Endocrinol Metab. 2015 Dec;100(12):E1540-9. doi: 10.1210/jc.2015-2763. Epub 2015 Oct 2.

PMID:
26431509
12.

Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family.

Babiker O, Flanagan SE, Ellard S, Al Girim H, Hussain K, Senniappan S.

J Pediatr Endocrinol Metab. 2015 Sep;28(9-10):1073-7. doi: 10.1515/jpem-2015-0033.

PMID:
25915078
13.

Novel mutation c.597_598dup in exon 5 of ABCC8 gene causing congenital hyperinsulinism.

Jindal R, Ahmad A, Siddiqui MA, Kochar IS, Wangnoo SK.

Diabetes Metab Syndr. 2014 Jan-Mar;8(1):45-7. doi: 10.1016/j.dsx.2013.02.018. Epub 2013 Mar 26.

PMID:
24661758
14.

Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism.

Saint-Martin C, Zhou Q, Martin GM, Vaury C, Leroy G, Arnoux JB, de Lonlay P, Shyng SL, Bellanné-Chantelot C.

Clin Genet. 2015 May;87(5):448-54. doi: 10.1111/cge.12428. Epub 2014 Jun 6.

15.

The evolving course of HNF4A hyperinsulinaemic hypoglycaemia--a case series.

McGlacken-Byrne SM, Hawkes CP, Flanagan SE, Ellard S, McDonnell CM, Murphy NP.

Diabet Med. 2014 Jan;31(1):e1-5. doi: 10.1111/dme.12259.

PMID:
23796040
16.

An Egyptian case of congenital hyperinsulinism of infancy due to a novel mutation in KCNJ11 encoding Kir6.2 and response to octreotide.

Sherif EM, Abdelmaksoud AA, Elbarbary NS, Njølstad PR.

Acta Diabetol. 2013 Oct;50(5):801-5. doi: 10.1007/s00592-010-0217-1. Epub 2010 Aug 5.

PMID:
20686794
17.

Molecular mechanisms of congenital hyperinsulinism.

Rahman SA, Nessa A, Hussain K.

J Mol Endocrinol. 2015 Apr;54(2):R119-29. doi: 10.1530/JME-15-0016. Epub 2015 Mar 2. Review.

PMID:
25733449
18.

Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees.

Flanagan SE, Patch AM, Locke JM, Akcay T, Simsek E, Alaei M, Yekta Z, Desai M, Kapoor RR, Hussain K, Ellard S.

J Clin Endocrinol Metab. 2011 Mar;96(3):E498-502. doi: 10.1210/jc.2010-1906. Epub 2011 Jan 20.

19.

Hyperinsulinemic Hypoglycemia of Infancy due to Novel HADH Mutation in Two Siblings.

Satapathy AK, Jain V, Ellard S, Flanagan SE.

Indian Pediatr. 2016 Oct 8;53(10):912-913.

20.

Nifedipine in Congenital Hyperinsulinism - A Case Report.

Khawash P, Hussain K, Flanagan SE, Chatterjee S, Basak D.

J Clin Res Pediatr Endocrinol. 2015 Jun;7(2):151-4. doi: 10.4274/jcrpe.1978.

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