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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

311 related articles for article (PubMed ID: 17551476)

  • 1. Hyperinsulinism in infancy--genetic aspects.
    Darendeliler F; Bas F
    Pediatr Endocrinol Rev; 2006 Aug; 3 Suppl 3():521-6. PubMed ID: 17551476
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Congenital hyperinsulinism in newborn and infant].
    Giurgea I; Ribeiro MJ; Boddaert N; Touati G; Robert JJ; Saudubray JM; Jaubert F; Bellanné-Chantelot C; Brunelle F; Nihoul-Fékété C; de Lonlay P
    Arch Pediatr; 2005 Nov; 12(11):1628-35. PubMed ID: 16198094
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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. PubMed ID: 16429405
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetics of congenital hyperinsulinism.
    Fournet JC; Junien C
    Endocr Pathol; 2004; 15(3):233-40. PubMed ID: 15640549
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.
    Tornovsky S; Crane A; Cosgrove KE; Hussain K; Lavie J; Heyman M; Nesher Y; Kuchinski N; Ben-Shushan E; Shatz O; Nahari E; Potikha T; Zangen D; Tenenbaum-Rakover Y; de Vries L; Argente J; Gracia R; Landau H; Eliakim A; Lindley K; Dunne MJ; Aguilar-Bryan L; Glaser B
    J Clin Endocrinol Metab; 2004 Dec; 89(12):6224-34. PubMed ID: 15579781
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular mechanisms of neonatal hyperinsulinism.
    Giurgea I; Bellanné-Chantelot C; Ribeiro M; Hubert L; Sempoux C; Robert JJ; Blankenstein O; Hussain K; Brunelle F; Nihoul-Fékété C; Rahier J; Jaubert F; de Lonlay P
    Horm Res; 2006; 66(6):289-96. PubMed ID: 17003566
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.
    Gloyn AL; Siddiqui J; Ellard S
    Hum Mutat; 2006 Mar; 27(3):220-31. PubMed ID: 16416420
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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. PubMed ID: 18596924
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 521(1):160-5. PubMed ID: 23506826
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The genetic basis of congenital hyperinsulinism.
    James C; Kapoor RR; Ismail D; Hussain K
    J Med Genet; 2009 May; 46(5):289-99. PubMed ID: 19254908
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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 Apr; 168(4):557-64. PubMed ID: 23345197
    [TBL] [Abstract][Full Text] [Related]  

  • 12. ABCC8 and KCNJ11 molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism.
    Bellanné-Chantelot C; Saint-Martin C; Ribeiro MJ; Vaury C; Verkarre V; Arnoux JB; Valayannopoulos V; Gobrecht S; Sempoux C; Rahier J; Fournet JC; Jaubert F; Aigrain Y; Nihoul-Fékété C; de Lonlay P
    J Med Genet; 2010 Nov; 47(11):752-9. PubMed ID: 20685672
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell.
    Oçal G; Flanagan SE; Hacihamdioğlu B; Berberoğlu M; Siklar Z; Ellard S; Savas Erdeve S; Okulu E; Akin IM; Atasay B; Arsan S; Yağmurlu A
    J Pediatr Endocrinol Metab; 2011; 24(11-12):1019-23. PubMed ID: 22308858
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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; 15(7):993-1000. PubMed ID: 12199344
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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. PubMed ID: 23275527
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Diazoxide-unresponsive congenital hyperinsulinism in children with dominant mutations of the β-cell sulfonylurea receptor SUR1.
    Macmullen CM; Zhou Q; Snider KE; Tewson PH; Becker SA; Aziz AR; Ganguly A; Shyng SL; Stanley CA
    Diabetes; 2011 Jun; 60(6):1797-804. PubMed ID: 21536946
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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. PubMed ID: 17466004
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. KATP channel mutations in congenital hyperinsulinism.
    Saint-Martin C; Arnoux JB; de Lonlay P; Bellanné-Chantelot C
    Semin Pediatr Surg; 2011 Feb; 20(1):18-22. PubMed ID: 21185999
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.