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Items: 1 to 20 of 87

1.

Analysis on the pathogenic genes of 60 Chinese children with congenital hyperinsulinemia.

Xu ZD, Zhang W, Liu M, Wang HM, Hui PP, Liang XJ, Yan J, Wu YJ, Sang YM, Zhu C, Ni GC.

Endocr Connect. 2018 Nov 12;7(12):1251-1261. doi: 10.1530/EC-18-0240.

2.

Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.

Fan ZC, Ni JW, Yang L, Hu LY, Ma SM, Mei M, Sun BJ, Wang HJ, Zhou WH.

Mol Genet Genomic Med. 2015 Jun 29;3(6):526-36. doi: 10.1002/mgg3.162. eCollection 2015 Nov.

3.

Clinical Management and Gene Mutation Analysis of Children with Congenital Hyperinsulinism in South China

Xu A, Cheng J, Sheng H, Wen Z, Lin Y, Zhou Z, Zeng C, Shao Y, Li C, Liu L, Li X.

J Clin Res Pediatr Endocrinol. 2019 Jun 18. doi: 10.4274/jcrpe.galenos.2019.2019.0046. [Epub ahead of print]

4.

Congenital Hyperinsulinism in China: A Review of Chinese Literature Over the Past 15 Years.

Wang WY, Sun Y, Zhao WT, Wu T, Wang L, Yuan TM, Yu HM.

J Clin Res Pediatr Endocrinol. 2017 Sep 1;9(3):194-201. doi: 10.4274/jcrpe.3934. Epub 2017 Mar 8. Review.

5.

[ABCC8, KCNJ11 and GLUD1 gene mutation analysis in congenital hyperinsulinism pedigree].

Xu ZD, Yu HF, Sang YM, Zhang YN, Yan J, Wu YJ, Zhu C, Ni GC.

Zhonghua Yi Xue Za Zhi. 2013 Apr 9;93(14):1089-92. Chinese.

PMID:
23902843
6.

The contribution of rapid KATP channel gene mutation analysis to the clinical management of children with congenital hyperinsulinism.

Banerjee I, Skae M, Flanagan SE, Rigby L, Patel L, Didi M, Blair J, Ehtisham S, Ellard S, Cosgrove KE, Dunne MJ, Clayton PE.

Eur J Endocrinol. 2011 May;164(5):733-40. doi: 10.1530/EJE-10-1136. Epub 2011 Mar 4.

PMID:
21378087
7.

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
8.

Clinical and genetic characterization of congenital hyperinsulinism in Spain.

Martínez R, Fernández-Ramos C, Vela A, Velayos T, Aguayo A, Urrutia I, Rica I, Castaño L; Spanish Congenital Hyperinsulinism Group.

Eur J Endocrinol. 2016 Jun;174(6):717-26. doi: 10.1530/EJE-16-0027.

PMID:
27188453
9.

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.

10.

Novel ABCC8 (SUR1) gene mutations in Asian Indian children with congenital hyperinsulinemic hypoglycemia.

Jahnavi S, Poovazhagi V, Kanthimathi S, Balamurugan K, Bodhini D, Yadav J, Jain V, Khadgawat R, Sikdar M, Bhavatharini A, Das AK, Kaur T, Mohan V, Radha V.

Ann Hum Genet. 2014 Sep;78(5):311-9. doi: 10.1111/ahg.12070.

11.

Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism.

Güven A, Cebeci AN, Ellard S, Flanagan SE.

J Clin Res Pediatr Endocrinol. 2016 Jun 5;8(2):197-204. doi: 10.4274/jcrpe.2408. Epub 2015 Dec 18.

12.

Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.

Gong C, Huang S, Su C, Qi Z, Liu F, Wu D, Cao B, Gu Y, Li W, Liang X, Liu M.

Pediatr Diabetes. 2016 May;17(3):227-34. doi: 10.1111/pedi.12254. Epub 2015 Feb 2.

PMID:
25639667
13.

18F-DOPA PET and enhanced CT imaging for congenital hyperinsulinism: initial UK experience from a technologist's perspective.

Meintjes M, Endozo R, Dickson J, Erlandsson K, Hussain K, Townsend C, Menezes L, Bomanji J.

Nucl Med Commun. 2013 Jun;34(6):601-8. doi: 10.1097/MNM.0b013e32836069d0.

PMID:
23571817
14.

Congenital hyperinsulinism.

Arnoux JB, de Lonlay P, Ribeiro MJ, Hussain K, Blankenstein O, Mohnike K, Valayannopoulos V, Robert JJ, Rahier J, Sempoux C, Bellanné C, Verkarre V, Aigrain Y, Jaubert F, Brunelle F, Nihoul-Fékété C.

Early Hum Dev. 2010 May;86(5):287-94. doi: 10.1016/j.earlhumdev.2010.05.003. Epub 2010 Jun 13. Review.

PMID:
20550977
15.

Genotype and phenotype analysis of a cohort of patients with congenital hyperinsulinism based on DOPA-PET CT scanning.

Ni J, Ge J, Zhang M, Hussain K, Guan Y, Cheng R, Xi L, Zheng Z, Ren S, Luo F.

Eur J Pediatr. 2019 Aug;178(8):1161-1169. doi: 10.1007/s00431-019-03408-6. Epub 2019 Jun 19.

16.

Paternally inherited ABCC8 mutation causing diffuse congenital hyperinsulinism.

Chandran S, Peng FY, Rajadurai VS, Lu YT, Chang KT, Flanagan SE, Ellard S, Hussain K.

Endocrinol Diabetes Metab Case Rep. 2013;2013:130041. doi: 10.1530/EDM-13-0041. Epub 2013 Nov 8.

17.

Genotype and phenotype correlations in Iranian patients with hyperinsulinaemic hypoglycaemia.

Senniappan S, Sadeghizadeh A, Flanagan SE, Ellard S, Hashemipour M, Hosseinzadeh M, Salehi M, Hussain K.

BMC Res Notes. 2015 Aug 13;8:350. doi: 10.1186/s13104-015-1319-1.

18.

The molecular mechanisms, diagnosis and management of congenital hyperinsulinism.

Senniappan S, Arya VB, Hussain K.

Indian J Endocrinol Metab. 2013 Jan;17(1):19-30. doi: 10.4103/2230-8210.107822.

19.

[Congenital hyperinsulinism in the north-east Netherlands. Clinical features and DNA diagnostics in 22 children].

Verheul JC, Ris-Stalpers C, Bikker H, Bakker-van Waarde WM, Noordam C.

Ned Tijdschr Geneeskd. 2011;155(32):A3343. Dutch.

PMID:
21835061
20.

A Case Series: Congenital Hyperinsulinism.

Alaei MR, Akbaroghli S, Keramatipour M, Alaei A.

Int J Endocrinol Metab. 2016 Sep 10;14(4):e37311. doi: 10.5812/ijem.37311. eCollection 2016 Oct.

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