메뉴 건너뛰기




Volumn 8, Issue 3, 2003, Pages 259-265

Surgery of persistent hyperinsulinaemic hypoglycaemia

Author keywords

Hyperinsulinism; Hypoglycaemia; Management

Indexed keywords

ADENOSINE TRIPHOSPHATE; CHLOROTHIAZIDE; DIAZOXIDE; GLUCAGON; INSULIN; NIFEDIPINE; OCTREOTIDE; SOMATOSTATIN;

EID: 0042848552     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1084-2756(03)00027-7     Document Type: Article
Times cited : (9)

References (65)
  • 2
    • 0036135191 scopus 로고    scopus 로고
    • Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases
    • de Lonlay P, Fournet JC, Touati G et al. Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases. Eur J Pediatr 2002;161:37-48.
    • (2002) Eur J Pediatr , vol.161 , pp. 37-48
    • De Lonlay, P.1    Fournet, J.C.2    Touati, G.3
  • 3
    • 0036306878 scopus 로고    scopus 로고
    • Persistent hyperinsulinaemic hypoglycaemia
    • de Lonlay P, Touati G, Robert JJ et al. Persistent hyperinsulinaemic hypoglycaemia. Semin Neonatal 2002;7: 95-100.
    • (2002) Semin Neonatal , vol.7 , pp. 95-100
    • De Lonlay, P.1    Touati, G.2    Robert, J.J.3
  • 4
    • 0034009959 scopus 로고    scopus 로고
    • Hyperinsulinism of the newborn
    • Glaser B. Hyperinsulinism of the newborn. Semin Perinatol 2000;24:150-63.
    • (2000) Semin Perinatol , vol.24 , pp. 150-163
    • Glaser, B.1
  • 6
    • 0015881533 scopus 로고
    • Suppression of insulin release by fish-insulin-induced hypoglycaemia: With reference to the diagnosis of insulinomas
    • Turner RC, Johnson PC. Suppression of insulin release by fish-insulin-induced hypoglycaemia: with reference to the diagnosis of insulinomas. Lancet 1973;1:1483-5.
    • (1973) Lancet , vol.1 , pp. 1483-1485
    • Turner, R.C.1    Johnson, P.C.2
  • 7
    • 0019416744 scopus 로고
    • Nesidioblastosis of the pancreas: Definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia
    • Aynsley-Green A, Polak JM, Bloom SR et al. Nesidioblastosis of the pancreas: definition of the syndrome and the management of the severe neonatal hyperinsulinaemic hypoglycaemia. Arch Dis Child 1981;56:496-508.
    • (1981) Arch Dis Child , vol.56 , pp. 496-508
    • Aynsley-Green, A.1    Polak, J.M.2    Bloom, S.R.3
  • 8
    • 0029814438 scopus 로고    scopus 로고
    • Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease
    • Morris AA, Thekekara A, Wilks Z et al. Evaluation of fasts for investigating hypoglycaemia or suspected metabolic disease. Arch Dis Child 1996;75:115-9.
    • (1996) Arch Dis Child , vol.75 , pp. 115-119
    • Morris, A.A.1    Thekekara, A.2    Wilks, Z.3
  • 9
    • 0033560942 scopus 로고    scopus 로고
    • The causes of neonatal hypoglycemia
    • Stanley CA, Baker L. The causes of neonatal hypoglycemia. N Engl J Med 1999;340:1200-1.
    • (1999) N Engl J Med , vol.340 , pp. 1200-1201
    • Stanley, C.A.1    Baker, L.2
  • 10
    • 0036304967 scopus 로고    scopus 로고
    • Clinical approach to inherited metabolic disorders in neonates: An overview
    • Saudubray JM, Nassogne MC, de Lonlay P et al. Clinical approach to inherited metabolic disorders in neonates: an overview. Semin Neonatal 2002;7:3-15.
    • (2002) Semin Neonatal , vol.7 , pp. 3-15
    • Saudubray, J.M.1    Nassogne, M.C.2    De Lonlay, P.3
  • 11
    • 19244373980 scopus 로고    scopus 로고
    • Genetic hypoglycaemia in infancy and childhood: Pathophysiology and diagnosis
    • Saudubray JM, de Lonlay P, Touati G et al. Genetic hypoglycaemia in infancy and childhood: pathophysiology and diagnosis. J Inherit Metab Dis 2000;23:197-214.
    • (2000) J Inherit Metab Dis , vol.23 , pp. 197-214
    • Saudubray, J.M.1    De Lonlay, P.2    Touati, G.3
  • 12
    • 0031041271 scopus 로고    scopus 로고
    • Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor
    • Dunne MJ, Kane C, Shepherd RM et al. Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor. N Engl J Med 1997;336:703-6.
    • (1997) N Engl J Med , vol.336 , pp. 703-706
    • Dunne, M.J.1    Kane, C.2    Shepherd, R.M.3
  • 13
    • 0029658788 scopus 로고    scopus 로고
    • Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy
    • Kane C, Shepherd RM, Squires PE et al. Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy. Nat Med 1996; 2:1344-7.
    • (1996) Nat Med , vol.2 , pp. 1344-1347
    • Kane, C.1    Shepherd, R.M.2    Squires, P.E.3
  • 14
    • 0031895737 scopus 로고    scopus 로고
    • Ions and genes in persistent hyperinsulinaemic hypoglycaemia in infancy: A commentary on the implications for tailoring treatment to disease pathogenesis
    • Aynsley-Green A, Dunne MJ, James RF et al. Ions and genes in persistent hyperinsulinaemic hypoglycaemia in infancy: a commentary on the implications for tailoring treatment to disease pathogenesis. J Pediatr Endocrinol Metab 1998; 11 (Suppl 1):121-9.
    • (1998) J Pediatr Endocrinol Metab , vol.11 , Issue.SUPPL. 1 , pp. 121-129
    • Aynsley-Green, A.1    Dunne, M.J.2    James, R.F.3
  • 15
    • 0034084749 scopus 로고    scopus 로고
    • Persistent hyperinsulinaemic hyperglycaemia of infancy-derived cells; Implications for beta-cells that replicate in vitro
    • Dunne MJ, Shepherd RM, Cosgrove KE et al. Persistent hyperinsulinaemic hyperglycaemia of infancy-derived cells; implications for beta-cells that replicate in vitro. J Mol Endocrinol 2000;24:313-20.
    • (2000) J Mol Endocrinol , vol.24 , pp. 313-320
    • Dunne, M.J.1    Shepherd, R.M.2    Cosgrove, K.E.3
  • 16
    • 0034097830 scopus 로고    scopus 로고
    • Ions, genes and insulin release: From basic science to clinical disease. Based on the 1998 R. D. Lawrence lecture
    • Dunne MJ. Ions, genes and insulin release: from basic science to clinical disease. Based on the 1998 R. D. Lawrence lecture. Diabet Med 2000;17:91-104.
    • (2000) Diabet Med , vol.17 , pp. 91-104
    • Dunne, M.J.1
  • 17
    • 0033026937 scopus 로고    scopus 로고
    • Potassium channels, sulphonylurea receptors and control of insulin release
    • Dunne MJ, Cosgrove KE, Shepherd RM et al. Potassium channels, sulphonylurea receptors and control of insulin release. Trends Endocrinol Metab 1999;10:146-52.
    • (1999) Trends Endocrinol Metab , vol.10 , pp. 146-152
    • Dunne, M.J.1    Cosgrove, K.E.2    Shepherd, R.M.3
  • 18
    • 0034064505 scopus 로고    scopus 로고
    • Hyperinsulinism of infancy: Towards an understanding of unregulated insulin release. European network for research into hyperinsulinism in infancy
    • Shepherd RM, Cosgrove KE, O'Brien RE et al. Hyperinsulinism of infancy: towards an understanding of unregulated insulin release. European network for research into hyperinsulinism in infancy. Arch Dis Child Fetal Neonatal Ed 2000; 82:F87-97.
    • (2000) Arch Dis Child Fetal Neonatal Ed , vol.82
    • Shepherd, R.M.1    Cosgrove, K.E.2    O'Brien, R.E.3
  • 19
    • 0033822063 scopus 로고    scopus 로고
    • A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene
    • Bitner-Glindzicz M, Lindley KJ, Rutland P et al. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene. Nat Genet 2000;26:56-60.
    • (2000) Nat Genet , vol.26 , pp. 56-60
    • Bitner-Glindzicz, M.1    Lindley, K.J.2    Rutland, P.3
  • 20
    • 0344629350 scopus 로고    scopus 로고
    • A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland
    • Otonkoski T, Ammala C, Huopio H et al. A point mutation inactivating the sulfonylurea receptor causes the severe form of persistent hyperinsulinemic hypoglycemia of infancy in Finland. Diabetes 1999;48:408-15.
    • (1999) Diabetes , vol.48 , pp. 408-415
    • Otonkoski, T.1    Ammala, C.2    Huopio, H.3
  • 21
    • 0029756638 scopus 로고    scopus 로고
    • Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy
    • Thomas PM, Wohllk N, Huang E et al. Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy. Am J Hum Genet 1996;59:510-8.
    • (1996) Am J Hum Genet , vol.59 , pp. 510-518
    • Thomas, P.M.1    Wohllk, N.2    Huang, E.3
  • 22
    • 0029021696 scopus 로고
    • Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
    • Thomas PM, Cote GJ, Wohllk N et al. Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy. Science 1995; 268:426-9.
    • (1995) Science , vol.268 , pp. 426-429
    • Thomas, P.M.1    Cote, G.J.2    Wohllk, N.3
  • 23
    • 0035142144 scopus 로고    scopus 로고
    • Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations
    • Grimberg A, Ferry RJ Jr, Kelly A et al. Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations. Diabetes 2001; 50:322-8.
    • (2001) Diabetes , vol.50 , pp. 322-328
    • Grimberg, A.1    Ferry R.J., Jr.2    Kelly, A.3
  • 24
    • 15644367096 scopus 로고    scopus 로고
    • A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism
    • Nestorowicz A, Inagaki N, Gonoi T et al. A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism. Diabetes 1997; 46:1743-8.
    • (1997) Diabetes , vol.46 , pp. 1743-1748
    • Nestorowicz, A.1    Inagaki, N.2    Gonoi, T.3
  • 25
    • 0029658241 scopus 로고    scopus 로고
    • Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
    • Nestorowicz A, Wilson BA, Schoor KP et al. Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews. Hum Mol Genet 1996; 5:1813-22.
    • (1996) Hum Mol Genet , vol.5 , pp. 1813-1822
    • Nestorowicz, A.1    Wilson, B.A.2    Schoor, K.P.3
  • 26
    • 0036320906 scopus 로고    scopus 로고
    • KATP channels and insulin secretion disorders
    • Huopio H, Shyng SL, Otonkoski T et al. KATP channels and insulin secretion disorders. Am J Physiol 2002;283:E207-16.
    • (2002) Am J Physiol , vol.283
    • Huopio, H.1    Shyng, S.L.2    Otonkoski, T.3
  • 27
    • 0035145905 scopus 로고    scopus 로고
    • Hyperinsulinism of infancy: The regulated release of insulin by KATP channel-independent pathways
    • Straub SG, Cosgrove KE, Ammala C et al. Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways. Diabetes 2001;50:329-39.
    • (2001) Diabetes , vol.50 , pp. 329-339
    • Straub, S.G.1    Cosgrove, K.E.2    Ammala, C.3
  • 28
    • 0035956875 scopus 로고    scopus 로고
    • Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy
    • Cartier EA, Conti LR, Vandenberg CA et al. Defective trafficking and function of KATP channels caused by a sulfonylurea receptor 1 mutation associated with persistent hyperinsulinemic hypoglycemia of infancy. Proc Natl Acad Sci USA 2001;98:2882-7.
    • (2001) Proc Natl Acad Sci USA , vol.98 , pp. 2882-2887
    • Cartier, E.A.1    Conti, L.R.2    Vandenberg, C.A.3
  • 29
    • 0035929661 scopus 로고    scopus 로고
    • Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familiar hyperinsulinism
    • Partridge CJ, Beech DJ, Sivaprasadarao A. Identification and pharmacological correction of a membrane trafficking defect associated with a mutation in the sulfonylurea receptor causing familiar hyperinsulinism. J Biol Chem 2001; 276:35947-52.
    • (2001) J Biol Chem , vol.276 , pp. 35947-35952
    • Partridge, C.J.1    Beech, D.J.2    Sivaprasadarao, A.3
  • 30
    • 0037053340 scopus 로고    scopus 로고
    • Identification of a familial hyperinsulinism-causing mutation in the sulfonylurea receptor 1 that prevents normal trafficking and function of KATP channels
    • Taschenberger G, Mougey A, Shen S et al. Identification of a familial hyperinsulinism-causing mutation in the sulfonylurea receptor 1 that prevents normal traffickin trafficking and function of KATP channels. J Biol Chem 2002;277:17139-46.
    • (2002) J Biol Chem , vol.277 , pp. 17139-17146
    • Taschenberger, G.1    Mougey, A.2    Shen, S.3
  • 31
    • 0030955295 scopus 로고    scopus 로고
    • Therapy for persistent hyperinsulinemic hypoglycemia of infancy. Understanding the responsiveness of beta cells to diazoxide and somatostatin
    • Kane C, Lindley KJ, Johnson PR et at. Therapy for persistent hyperinsulinemic hypoglycemia of infancy. Understanding the responsiveness of beta cells to diazoxide and somatostatin. J Clin Invest 1997;100:1888-93.
    • (1997) J Clin Invest , vol.100 , pp. 1888-1893
    • Kane, C.1    Lindley, K.J.2    Johnson, P.R.3
  • 32
    • 0033803049 scopus 로고    scopus 로고
    • Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1
    • Huopio H, Reimann F, Ashfield R et al. Dominantly inherited hyperinsulinism caused by a mutation in the sulfonylurea receptor type 1. J Clin Invest 2000;106:897-906.
    • (2000) J Clin Invest , vol.106 , pp. 897-906
    • Huopio, H.1    Reimann, F.2    Ashfield, R.3
  • 33
    • 0034029974 scopus 로고    scopus 로고
    • Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: Predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA contributing investigators
    • Stanley CA, Fang J, Kutyna K et al. Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA contributing investigators. Diabetes 2000;49:667-73.
    • (2000) Diabetes , vol.49 , pp. 667-673
    • Stanley, C.A.1    Fang, J.2    Kutyna, K.3
  • 34
    • 0032493123 scopus 로고    scopus 로고
    • Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
    • Stanley CA, Lieu YK, Hsu BY et al. Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene. N Engl J Med 1998; 338:1352-7.
    • (1998) N Engl J Med , vol.338 , pp. 1352-1357
    • Stanley, C.A.1    Lieu, Y.K.2    Hsu, B.Y.3
  • 35
    • 0035128978 scopus 로고    scopus 로고
    • Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome
    • Santer R, Kinner M, Passarge M et al. Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome. Hum Genet 2001;108:66-71.
    • (2001) Hum Genet , vol.108 , pp. 66-71
    • Santer, R.1    Kinner, M.2    Passarge, M.3
  • 36
    • 0034864167 scopus 로고    scopus 로고
    • Hyperinsulinism and hyperammonemia syndrome: Report of twelve unrelated patients
    • de Lonlay P, Benetti C, Fouque F et al. Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients. Pediatr Res 2001;50:353-7.
    • (2001) Pediatr Res , vol.50 , pp. 353-357
    • De Lonlay, P.1    Benetti, C.2    Fouque, F.3
  • 37
    • 0034902277 scopus 로고    scopus 로고
    • Hyperinsulinism in short-chain 1-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion
    • Clayton PT, Eaton S, Aynsley-Green A et al. Hyperinsulinism in short-chain 1-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion. J Clin Invest 2001;108:457-65.
    • (2001) J Clin Invest , vol.108 , pp. 457-465
    • Clayton, P.T.1    Eaton, S.2    Aynsley-Green, A.3
  • 38
    • 17444448342 scopus 로고    scopus 로고
    • Phosphomannose isomerase deficiency: A carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation
    • Jaeken J, Matthijs G, Saudubray JM et al. Phosphomannose isomerase deficiency: a carbohydrate-deficient glycoprotein syndrome with hepatic-intestinal presentation. Am J Hum Genet 1998;62:1535-9.
    • (1998) Am J Hum Genet , vol.62 , pp. 1535-1539
    • Jaeken, J.1    Matthijs, G.2    Saudubray, J.M.3
  • 39
    • 0032556969 scopus 로고    scopus 로고
    • Familial hyperinsulinism caused by an activating glucokinase mutation
    • Glaser B, Kesavan P, Heyman M et al. Familial hyperinsulinism caused by an activating glucokinase mutation. N Engl J Med 1998;338:226-30.
    • (1998) N Engl J Med , vol.338 , pp. 226-230
    • Glaser, B.1    Kesavan, P.2    Heyman, M.3
  • 40
    • 0031936418 scopus 로고    scopus 로고
    • Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: The pathologist's role
    • Rahier J, Sempoux C, Fournet JC et al. Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role. Histopathology 1998; 32:15-9.
    • (1998) Histopathology , vol.32 , pp. 15-19
    • Rahier, J.1    Sempoux, C.2    Fournet, J.C.3
  • 41
    • 0029603625 scopus 로고
    • Nesidioblastosis and persistent neonatal hyperinsulinism
    • Sempoux C, Poggi F, Brunelle F et at. Nesidioblastosis and persistent neonatal hyperinsulinism. Diabetes Metab 1995; 21:402-7.
    • (1995) Diabetes Metab , vol.21 , pp. 402-407
    • Sempoux, C.1    Poggi, F.2    Brunelle, F.3
  • 42
    • 0030880778 scopus 로고    scopus 로고
    • Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
    • de Lonlay P, Fournet JC, Rahier J et al. Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy. J Clin Invest 1997;100:802-7.
    • (1997) J Clin Invest , vol.100 , pp. 802-807
    • De Lonlay, P.1    Fournet, J.C.2    Rahier, J.3
  • 43
    • 0032447019 scopus 로고    scopus 로고
    • Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia
    • Fournet JC, Verkarre V, de Lonlay P et al. Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia. Ann Endocrinol (Paris) 1998;59:485-91.
    • (1998) Ann Endocrinol (Paris) , vol.59 , pp. 485-491
    • Fournet, J.C.1    Verkarre, V.2    De Lonlay, P.3
  • 44
    • 0034970925 scopus 로고    scopus 로고
    • 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 et al. 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. Am J Pathol 2001;158:2177-84.
    • (2001) Am J Pathol , vol.158 , pp. 2177-2184
    • Fournet, J.C.1    Mayaud, C.2    De Lonlay, P.3
  • 45
    • 0033909936 scopus 로고    scopus 로고
    • Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism
    • Fournet JC, Mayaud C, de Lonlay P et al. Loss of imprinted genes and paternal SUR1 mutations lead to focal form of congenital hyperinsulinism. Horm Res 2000;53(Suppl 1): 2-6.
    • (2000) Horm Res , vol.53 , Issue.SUPPL. 1 , pp. 2-6
    • Fournet, J.C.1    Mayaud, C.2    De Lonlay, P.3
  • 46
    • 0032190017 scopus 로고    scopus 로고
    • 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 et al. Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia. J Clin Invest 1998; 102:1286-91.
    • (1998) J Clin Invest , vol.102 , pp. 1286-1291
    • Verkarre, V.1    Fournet, J.C.2    De Lonlay, P.3
  • 48
    • 0035122423 scopus 로고    scopus 로고
    • Focal or diffuse lesions in persistent hyperinsulinemic hypoglycemia of infancy: Concerns about interpretation of intraoperative frozen sections
    • Smith VV, Malone M, Risdon RA. Focal or diffuse lesions in persistent hyperinsulinemic hypoglycemia of infancy: concerns about interpretation of intraoperative frozen sections. Pediatr Dev Pathol 2001;4:138-43.
    • (2001) Pediatr Dev Pathol , vol.4 , pp. 138-143
    • Smith, V.V.1    Malone, M.2    Risdon, R.A.3
  • 49
    • 0036154369 scopus 로고    scopus 로고
    • Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: A report of 45 cases from 1983 to 2000
    • Cretolle C, Fekete CN, Jan D et al. Partial elective pancreatectomy is curative in focal form of permanent hyperinsulinemic hypoglycaemia in infancy: a report of 45 cases from 1983 to 2000. J Pediatr Surg 2002;37:155-8.
    • (2002) J Pediatr Surg , vol.37 , pp. 155-158
    • Cretolle, C.1    Fekete, C.N.2    Jan, D.3
  • 50
    • 0028813928 scopus 로고
    • Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: High incidence of diabetes mellitus and persistent beta-cell dysfunction at long-term follow-up
    • Leibowitz G, Glaser B, Higazi AA et al. Hyperinsulinemic hypoglycemia of infancy (nesidioblastosis) in clinical remission: high incidence of diabetes mellitus and persistent beta-cell dysfunction at long-term follow-up. J Clin Endocrinol Metab 1995;80:386-92.
    • (1995) J Clin Endocrinol Metab , vol.80 , pp. 386-392
    • Leibowitz, G.1    Glaser, B.2    Higazi, A.A.3
  • 51
    • 0025651165 scopus 로고
    • Diabetes mellitus 14 years after subtotal pancreatectomy for neonatal hypednsulinism
    • Labrune P, Lechevallier S, Rautt M et al. Diabetes mellitus 14 years after subtotal pancreatectomy for neonatal hypednsulinism. J Pediatr Surg 1990;25:1246-7.
    • (1990) J Pediatr Surg , vol.25 , pp. 1246-1247
    • Labrune, P.1    Lechevallier, S.2    Rautt, M.3
  • 52
    • 0029098644 scopus 로고
    • Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
    • Dubois J, Brunelle F, Touati G et al. Hyperinsulinism in children: diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases. Pediatr Radiol 1995;25:512-6.
    • (1995) Pediatr Radiol , vol.25 , pp. 512-516
    • Dubois, J.1    Brunelle, F.2    Touati, G.3
  • 53
    • 0024495419 scopus 로고
    • Pancreatic venous samplings in infants and children with primary hyperinsulinism
    • Brunelle F, Negre V, Barth MO et al. Pancreatic venous samplings in infants and children with primary hyperinsulinism. Pediatr Radiol 1989;19:100-3.
    • (1989) Pediatr Radiol , vol.19 , pp. 100-103
    • Brunelle, F.1    Negre, V.2    Barth, M.O.3
  • 54
    • 0034874373 scopus 로고    scopus 로고
    • Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy
    • Chigot V, de Lontay P, Nassogne MC et al. Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy. Pediatr Radiol 2001;31:650-5.
    • (2001) Pediatr Radiol , vol.31 , pp. 650-655
    • Chigot, V.1    De Lontay, P.2    Nassogne, M.C.3
  • 55
    • 0031891277 scopus 로고    scopus 로고
    • Intra-arteriat calcium stimulation test in the investigation of hyperinsulinaemic hypoglycaemia
    • Abernethy LJ, Davidson DC, Lamont GL et al. Intra-arteriat calcium stimulation test in the investigation of hyperinsulinaemic hypoglycaemia. Arch Dis Child 1998; 78:359-63.
    • (1998) Arch Dis Child , vol.78 , pp. 359-363
    • Abernethy, L.J.1    Davidson, D.C.2    Lamont, G.L.3
  • 56
    • 0033846802 scopus 로고    scopus 로고
    • Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism
    • Ferry RJ Jr, Kelly A, Grimberg A et al. Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism. J Pediatr 2000;137:239-46.
    • (2000) J Pediatr , vol.137 , pp. 239-246
    • Ferry R.J., Jr.1    Kelly, A.2    Grimberg, A.3
  • 57
    • 0031856155 scopus 로고    scopus 로고
    • Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: A retrospective review of 77 cases and analysis of efficacy-predicting criteria
    • Touati G, Poggi-Travert F, Ogier DB et al. Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteria. Eur J Pediatr 1998;157:628-33.
    • (1998) Eur J Pediatr , vol.157 , pp. 628-633
    • Touati, G.1    Poggi-Travert, F.2    Ogier, D.B.3
  • 58
    • 9344222798 scopus 로고    scopus 로고
    • Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade
    • Lindley KJ, Dunne MJ, Kane C et al. Ionic control of beta cell function in nesidioblastosis. A possible therapeutic role for calcium channel blockade. Arch Dis Child 1996;74:373-8.
    • (1996) Arch Dis Child , vol.74 , pp. 373-378
    • Lindley, K.J.1    Dunne, M.J.2    Kane, C.3
  • 59
    • 0033452288 scopus 로고    scopus 로고
    • Successful therapy with calcium channel blocker (nifedipine) in persistent neonatal hyperinsulinemic hypoglycemia of infancy
    • Bas F, Darendeliler F, Demirkol D et al. Successful therapy with calcium channel blocker (nifedipine) in persistent neonatal hyperinsulinemic hypoglycemia of infancy. J Pediatr Endocrinol Metab 1999;12:873-8.
    • (1999) J Pediatr Endocrinol Metab , vol.12 , pp. 873-878
    • Bas, F.1    Darendeliler, F.2    Demirkol, D.3
  • 60
    • 0027375645 scopus 로고
    • Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy
    • Glaser B, Hirsch HJ, Landau H. Persistent hyperinsulinemic hypoglycemia of infancy: long-term octreotide treatment without pancreatectomy. J Pediatr 1993;123:644-50.
    • (1993) J Pediatr , vol.123 , pp. 644-650
    • Glaser, B.1    Hirsch, H.J.2    Landau, H.3
  • 61
    • 0027374336 scopus 로고
    • Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism
    • Thornton PS, Alter CA, Katz LE et al. Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism. J Pediatr 1993;123:637-43.
    • (1993) J Pediatr , vol.123 , pp. 637-643
    • Thornton, P.S.1    Alter, C.A.2    Katz, L.E.3
  • 62
    • 0023901971 scopus 로고
    • Long-term use of somatostatin analogue SMS 201-995 in the treatment of hypoglycaemia due to nesidioblastosis
    • Wilson DC, Carson DJ, Quinn RJ. Long-term use of somatostatin analogue SMS 201-995 in the treatment of hypoglycaemia due to nesidioblastosis. Acta Paediatr Scand 1988; 77:467-70.
    • (1988) Acta Paediatr Scand , vol.77 , pp. 467-470
    • Wilson, D.C.1    Carson, D.J.2    Quinn, R.J.3
  • 63
    • 0023854783 scopus 로고
    • Pancreatic exocrine and endocrine function after subtotal pancreatectomy for nesidioblastosis
    • Dunger DB, Burns C, Ghale GK et al. Pancreatic exocrine and endocrine function after subtotal pancreatectomy for nesidioblastosis. J Pediatr Surg 1988;23:112-5.
    • (1988) J Pediatr Surg , vol.23 , pp. 112-115
    • Dunger, D.B.1    Burns, C.2    Ghale, G.K.3
  • 64
    • 0041595616 scopus 로고
    • Surgery for hyperinsulinaemic hypoglycaemia
    • Spitz L, Coran AG, editors. London: Chapman and Hall Medical
    • Spitz L. Surgery for hyperinsulinaemic hypoglycaemia. In: Spitz L, Coran AG, editors. Pediatric surgery. London: Chapman and Hall Medical 1995;618-22.
    • (1995) Pediatric Surgery , pp. 618-622
    • Spitz, L.1
  • 65
    • 0037240063 scopus 로고    scopus 로고
    • Surgical complications of pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy
    • McAndrew HF, Smith V, Spitz L. Surgical complications of pancreatectomy for persistent hyperinsulinaemic hypoglycaemia of infancy. J Pediatr Surg 2003;38:13-6.
    • (2003) J Pediatr Surg , vol.38 , pp. 13-16
    • McAndrew, H.F.1    Smith, V.2    Spitz, L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.