BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 16357843)

  • 1. Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism.
    Suchi M; MacMullen CM; Thornton PS; Adzick NS; Ganguly A; Ruchelli ED; Stanley CA
    Mod Pathol; 2006 Jan; 19(1):122-9. PubMed ID: 16357843
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism.
    Damaj L; le Lorch M; Verkarre V; Werl C; Hubert L; Nihoul-Fékété C; Aigrain Y; de Keyzer Y; Romana SP; Bellanne-Chantelot C; de Lonlay P; Jaubert F
    J Clin Endocrinol Metab; 2008 Dec; 93(12):4941-7. PubMed ID: 18796520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.
    Fournet JC; Mayaud C; de Lonlay P; Gross-Morand MS; Verkarre V; Castanet M; Devillers M; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
    Am J Pathol; 2001 Jun; 158(6):2177-84. PubMed ID: 11395395
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism.
    Giurgea I; Sempoux C; Bellanné-Chantelot C; Ribeiro M; Hubert L; Boddaert N; Saudubray JM; Robert JJ; Brunelle F; Rahier J; Jaubert F; Nihoul-Fékété C; de Lonlay P
    J Clin Endocrinol Metab; 2006 Oct; 91(10):4118-23. PubMed ID: 16882742
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [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]  

  • 6. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.
    Verkarre V; Fournet JC; de Lonlay P; Gross-Morand MS; Devillers M; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
    J Clin Invest; 1998 Oct; 102(7):1286-91. PubMed ID: 9769320
    [TBL] [Abstract][Full Text] [Related]  

  • 7. An ABCC8 gene mutation and mosaic uniparental isodisomy resulting in atypical diffuse congenital hyperinsulinism.
    Hussain K; Flanagan SE; Smith VV; Ashworth M; Day M; Pierro A; Ellard S
    Diabetes; 2008 Jan; 57(1):259-63. PubMed ID: 17942822
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation.
    Stanley CA; Thornton PS; Ganguly A; MacMullen C; Underwood P; Bhatia P; Steinkrauss L; Wanner L; Kaye R; Ruchelli E; Suchi M; Adzick NS
    J Clin Endocrinol Metab; 2004 Jan; 89(1):288-96. PubMed ID: 14715863
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Three novel pathogenic mutations in KATP channel genes and somatic imprinting alterations of the 11p15 region in pancreatic tissue in patients with congenital hyperinsulinism.
    Lee BH; Lee J; Kim JM; Kang M; Kim GH; Choi JH; Kim J; Kim CJ; Kim DY; Kim SC; Yoo HW
    Horm Res Paediatr; 2015; 83(3):204-10. PubMed ID: 25765446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia.
    Fournet JC; Verkarre V; De Lonlay P; Rahier J; Brunelle F; Robert JJ; Nihoul-Fékété C; Saudubray JM; Junien C
    Ann Endocrinol (Paris); 1998; 59(6):485-91. PubMed ID: 10189991
    [TBL] [Abstract][Full Text] [Related]  

  • 12. p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.
    Kassem SA; Ariel I; Thornton PS; Hussain K; Smith V; Lindley KJ; Aynsley-Green A; Glaser B
    Diabetes; 2001 Dec; 50(12):2763-9. PubMed ID: 11723059
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
    Glaser B; Ryan F; Donath M; Landau H; Stanley CA; Baker L; Barton DE; Thornton PS
    Diabetes; 1999 Aug; 48(8):1652-7. PubMed ID: 10426386
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hepatoblastoma in a child with a paternally-inherited ABCC8 mutation and mosaic paternal uniparental disomy 11p causing focal congenital hyperinsulinism.
    Calton EA; Temple IK; Mackay DJ; Lever M; Ellard S; Flanagan SE; Davies JH; Hussain K; Gray JC
    Eur J Med Genet; 2013 Feb; 56(2):114-7. PubMed ID: 23261959
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations.
    Suchi M; MacMullen C; Thornton PS; Ganguly A; Stanley CA; Ruchelli ED
    Pediatr Dev Pathol; 2003; 6(4):322-33. PubMed ID: 14692646
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The focal form of persistent hyperinsulinemic hypoglycemia of infancy: morphological and molecular studies show structural and functional differences with insulinoma.
    Sempoux C; Guiot Y; Dahan K; Moulin P; Stevens M; Lambot V; de Lonlay P; Fournet JC; Junien C; Jaubert F; Nihoul-Fekete C; Saudubray JM; Rahier J
    Diabetes; 2003 Mar; 52(3):784-94. PubMed ID: 12606521
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. Genotypes of the pancreatic beta-cell K-ATP channel and clinical phenotypes of Japanese patients with persistent hyperinsulinaemic hypoglycaemia of infancy.
    Ohkubo K; Nagashima M; Naito Y; Taguchi T; Suita S; Okamoto N; Fujinaga H; Tsumura K; Kikuchi K; Ono J
    Clin Endocrinol (Oxf); 2005 Apr; 62(4):458-65. PubMed ID: 15807877
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dominantly acting ABCC8 mutations in patients with medically unresponsive hyperinsulinaemic hypoglycaemia.
    Flanagan SE; Kapoor RR; Banerjee I; Hall C; Smith VV; Hussain K; Ellard S
    Clin Genet; 2011 Jun; 79(6):582-7. PubMed ID: 20573158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.