These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
9. 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; 8():350. PubMed ID: 26268944 [TBL] [Abstract][Full Text] [Related]
10. 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; 9(3):194-201. PubMed ID: 28270372 [TBL] [Abstract][Full Text] [Related]
11. Congenital hyperinsulinism: 2 case reports with different rare variants in ABCC8. Mouron-Hryciuk J; Stoppa-Vaucher S; Busiah K; Bouthors T; Antoniou MC; Jacot E; Brusgaard K; Christesen HT; Hussain K; Dwyer A; Roth-Kleiner M; Hauschild M Ann Pediatr Endocrinol Metab; 2021 Mar; 26(1):60-65. PubMed ID: 32871644 [TBL] [Abstract][Full Text] [Related]
13. 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 Nov; 11(4):400-409. PubMed ID: 31208162 [TBL] [Abstract][Full Text] [Related]
14. 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 Nov; 3(6):526-36. PubMed ID: 26740944 [TBL] [Abstract][Full Text] [Related]
16. Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism. Park SE; Flanagan SE; Hussain K; Ellard S; Shin CH; Yang SW Eur J Endocrinol; 2011 Jun; 164(6):919-26. PubMed ID: 21422196 [TBL] [Abstract][Full Text] [Related]
17. 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. PubMed ID: 19475716 [TBL] [Abstract][Full Text] [Related]
18. 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. PubMed ID: 25008049 [TBL] [Abstract][Full Text] [Related]
19. Congenital hyperinsulinism due to compound heterozygous mutations in ABCC8 responsive to diazoxide therapy. Taylor-Miller T; Houghton J; Munyard P; Kumar Y; Puvirajasinghe C; Giri D J Pediatr Endocrinol Metab; 2020 May; 33(5):671-674. PubMed ID: 32267248 [TBL] [Abstract][Full Text] [Related]
20. Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism. Männistö JME; Maria M; Raivo J; Kuulasmaa T; Otonkoski T; Huopio H; Laakso M J Clin Endocrinol Metab; 2020 Apr; 105(4):. PubMed ID: 32170320 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]