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    Results: 1 to 20 of 323

    1.

    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.PMID: 12606521 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    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.PMID: 11395395 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    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.PMID: 16357843 [PubMed - indexed for MEDLINE]Related articlesFree article

    4.

    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 1;102(7):1286-91.PMID: 9769320 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    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.PMID: 11723059 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    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.PMID: 10189991 [PubMed - indexed for MEDLINE]Related articles

    7.

    The focal form of persistent hyperinsulinemic hypoglycemia of infancy.

    Sempoux C, Guiot Y, Rahier J.

    Diabetes. 2001 Feb;50 Suppl 1:S182-3. No abstract available. PMID: 11272187 [PubMed - indexed for MEDLINE]Related articles

    8.

    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. Epub 2008 Sep 16.PMID: 18796520 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    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 Jul-Aug;15(7):993-1000.PMID: 12199344 [PubMed - indexed for MEDLINE]Related articles

    10.

    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.PMID: 10426386 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Characterization of genes encoding the pancreatic beta-cell ATP-sensitive K+ channel in persistent hyperinsulinemic hypoglycemia of infancy in Japanese patients.

    Someya T, Miki T, Sugihara S, Minagawa M, Yasuda T, Kohno Y, Seino S.

    Endocr J. 2000 Dec;47(6):715-22.PMID: 11228046 [PubMed - indexed for MEDLINE]Related articles

    12.

    Engineering a glucose-responsive human insulin-secreting cell line from islets of Langerhans isolated from a patient with persistent hyperinsulinemic hypoglycemia of infancy.

    MacFarlane WM, Chapman JC, Shepherd RM, Hashmi MN, Kamimura N, Cosgrove KE, O'Brien RE, Barnes PD, Hart AW, Docherty HM, Lindley KJ, Aynsley-Green A, James RF, Docherty K, Dunne MJ.

    J Biol Chem. 1999 Nov 26;274(48):34059-66.PMID: 10567373 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.

    Hussain K, Cosgrove KE, Shepherd RM, Luharia A, Smith VV, Kassem S, Gregory JW, Sivaprasadarao A, Christesen HT, Jacobsen BB, Brusgaard K, Glaser B, Maher EA, Lindley KJ, Hindmarsh P, Dattani M, Dunne MJ.

    J Clin Endocrinol Metab. 2005 Jul;90(7):4376-82. Epub 2005 Apr 5.PMID: 15811927 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland.

    Otonkoski T, Ammälä C, Huopio H, Cote GJ, Chapman J, Cosgrove K, Ashfield R, Huang E, Komulainen J, Ashcroft FM, Dunne MJ, Kere J, Thomas PM.

    Diabetes. 1999 Feb;48(2):408-15.PMID: 10334322 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy.

    Thomas PM, Wohllk N, Huang E, Kuhnle U, Rabl W, Gagel RF, Cote GJ.

    Am J Hum Genet. 1996 Sep;59(3):510-8.PMID: 8751851 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.

    Dunne MJ, Kane C, Shepherd RM, Sanchez JA, James RF, Johnson PR, Aynsley-Green A, Lu S, Clement JP 4th, Lindley KJ, Seino S, Aguilar-Bryan L.

    N Engl J Med. 1997 Mar 6;336(10):703-6. No abstract available. PMID: 9041101 [PubMed - indexed for MEDLINE]Related articles

    17.

    Hyperinsulinism: molecular aetiology of focal disease.

    Ryan F, Devaney D, Joyce C, Nestorowicz A, Permutt MA, Glaser B, Barton DE, Thornton PS.

    Arch Dis Child. 1998 Nov;79(5):445-7.PMID: 10193261 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism.

    Fournet JC, Mayaud C, de Lonlay P, Verkarre V, Rahier J, Brunelle F, Robert JJ, Nihoul-Fékété C, Saudubray JM, Junien C.

    Horm Res. 2000;53 Suppl 1:2-6.PMID: 10895035 [PubMed - indexed for MEDLINE]Related articles

    19.

    Clinical features of 52 neonates with hyperinsulinism.

    de Lonlay-Debeney P, Poggi-Travert F, Fournet JC, Sempoux C, Vici CD, Brunelle F, Touati G, Rahier J, Junien C, Nihoul-Fékété C, Robert JJ, Saudubray JM.

    N Engl J Med. 1999 Apr 15;340(15):1169-75.PMID: 10202168 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Facial appearance in persistent hyperinsulinemic hypoglycemia.

    de Lonlay P, Cormier-Daire V, Amiel J, Touati G, Goldenberg A, Fournet JC, Brunelle F, Nihoul-Fékété C, Rahier J, Junien C, Robert JJ, Saudubray JM.

    Am J Med Genet. 2002 Aug 1;111(2):130-3.PMID: 12210338 [PubMed - indexed for MEDLINE]Related articles

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