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Volumn 38, Issue 4, 2008, Pages 386-389

Case report: Pathological features of aberrant pancreatic development in congenital hyperinsulinism due to ABCC8 mutations

Author keywords

ABCC8 gene mutation; Congenital hyperinsulinism; Glucagon; Pancreatic development

Indexed keywords

DIAZOXIDE; GLUCAGON; INSULIN; OCTREOTIDE;

EID: 55949103758     PISSN: 00917370     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (9)
  • 1
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    • Diffuse and focal nesidioblastosis. A clinicopathological study of 24 patients with persistent neonatal hyperinsulinemic hypoglycemia
    • Goossens A, Gepts W, Saudubray JM, Bonnefont JP, Nihoul-Fekete, Heitz PU, Klöppel G. Diffuse and focal nesidioblastosis. A clinicopathological study of 24 patients with persistent neonatal hyperinsulinemic hypoglycemia. Am J Surg Pathol 1989;13:766-775.
    • (1989) Am J Surg Pathol , vol.13 , pp. 766-775
    • Goossens, A.1    Gepts, W.2    Saudubray, J.M.3    Bonnefont, J.P.4    Fekete, N.5    Heitz, P.U.6    Klöppel, G.7
  • 4
    • 0029836983 scopus 로고    scopus 로고
    • Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
    • Thomas P, Ye Y, Lightner E. Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet 1996;5:1809-1812.
    • (1996) Hum Mol Genet , vol.5 , pp. 1809-1812
    • Thomas, P.1    Ye, Y.2    Lightner, E.3
  • 5
    • 55949133814 scopus 로고    scopus 로고
    • Localized islet cell nuclear enlargement incongenital hyperinsulinism: A distinct clinicopathologic entity
    • Ernst LM, Suchi M, Stanley CA, Adzick NS, MacMullen C, Ruchelli ED. Localized islet cell nuclear enlargement incongenital hyperinsulinism: a distinct clinicopathologic entity. Mod Pathol 2007;20:287.
    • (2007) Mod Pathol , vol.20 , pp. 287
    • Ernst, L.M.1    Suchi, M.2    Stanley, C.A.3    Adzick, N.S.4    MacMullen, C.5    Ruchelli, E.D.6
  • 6
    • 0033932030 scopus 로고    scopus 로고
    • Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels
    • Sharma N, Crane A, Gonzalez G, Bryan J, Aguilar-Bryan L. Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels. Kidney Int 2000;57:803-808.
    • (2000) Kidney Int , vol.57 , pp. 803-808
    • Sharma, N.1    Crane, A.2    Gonzalez, G.3    Bryan, J.4    Aguilar-Bryan, L.5
  • 8
    • 34247863948 scopus 로고    scopus 로고
    • Genotype-phenotype association in patients with severe hyperinsulinism of infancy
    • Greer RM, Shan J, et al. Genotype-phenotype association in patients with severe hyperinsulinism of infancy. Pediatr Dev Pathol 2007;10:25-34.
    • (2007) Pediatr Dev Pathol , vol.10 , pp. 25-34
    • Greer, R.M.1    Shan, J.2
  • 9
    • 0015104472 scopus 로고
    • Beta cell nesidioblastosis in idiopathic hypoglycemia of infancy
    • Yakovac WC, Baker L, Hummeler K. Beta cell nesidioblastosis in idiopathic hypoglycemia of infancy. J Pediatr 1971;79:226-231.
    • (1971) J Pediatr , vol.79 , pp. 226-231
    • Yakovac, W.C.1    Baker, L.2    Hummeler, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.