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Volumn 12, Issue 11, 2005, Pages 1628-1635

Congenital hyperinsulinism in newborn and infant;L'hyperinsulinisme congénital du nouveau-né et du nourrisson

Author keywords

Hyperinsulinism, congenital; Hyperinsulinism, genetics; Hypoglycemia; Infant; Newborn; Pancreas, radionuclide imaging

Indexed keywords

DIAZOXIDE; FLUORINE 18; LEVODOPA; POTASSIUM CHANNEL;

EID: 27644528133     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2005.07.016     Document Type: Short Survey
Times cited : (7)

References (48)
  • 1
    • 0015593630 scopus 로고
    • Hypoglycemia in infancy and childhood. I
    • A.S. Pagliara, I.E. Karl, and M. Haymond Hypoglycemia in infancy and childhood. I J. Pediatr. 82 1973 365 379
    • (1973) J. Pediatr. , vol.82 , pp. 365-379
    • Pagliara, A.S.1    Karl, I.E.2    Haymond, M.3
  • 2
    • 0025233448 scopus 로고
    • Hypoglycemia in infancy: The need for a rational definition. a ciba foundation discussion meeting
    • M. Cornblath, R. Schwartz, and A. Aynsley-Green Hypoglycemia in infancy: the need for a rational definition. A ciba foundation discussion meeting Pediatrics 85 1990 834 837
    • (1990) Pediatrics , vol.85 , pp. 834-837
    • Cornblath, M.1    Schwartz, R.2    Aynsley-Green, A.3
  • 4
    • 0017617191 scopus 로고
    • Neonatal and infantile hypoglycemia due to insulin excess: New aspects of diagnosis and surgical management
    • C.G. Thomas Jr., L.E. Underwood, and C.N. Carney Neonatal and infantile hypoglycemia due to insulin excess: new aspects of diagnosis and surgical management Ann. Surg. 185 1977 505 517
    • (1977) Ann. Surg. , vol.185 , pp. 505-517
    • Thomas Jr., C.G.1    Underwood, L.E.2    Carney, C.N.3
  • 5
    • 0036135191 scopus 로고    scopus 로고
    • Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. a series of 175 cases
    • P. de Lonlay, J.C. Fournet, and G. Touati Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases Eur. J. Pediatr. 161 2002 37 48
    • (2002) Eur. J. Pediatr. , vol.161 , pp. 37-48
    • De Lonlay, P.1    Fournet, J.C.2    Touati, G.3
  • 6
    • 0037158471 scopus 로고    scopus 로고
    • Facial appearance in persistent hyperinsulinemic hypoglycemia
    • P. De Lonlay, V. Cormier-Daire, and J. Amiel Facial appearance in persistent hyperinsulinemic hypoglycemia Am. J. Med. Genet. 111 2002 130 133
    • (2002) Am. J. Med. Genet. , vol.111 , pp. 130-133
    • De Lonlay, P.1    Cormier-Daire, V.2    Amiel, J.3
  • 7
    • 0033510652 scopus 로고    scopus 로고
    • Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose
    • P. de Lonlay, M. Cuer, and S. Vuillaumier-Barrot Hyperinsulinemic hypoglycemia as a presenting sign in phosphomannose isomerase deficiency: A new manifestation of carbohydrate-deficient glycoprotein syndrome treatable with mannose J. Pediatr. 135 1999 379 383
    • (1999) J. Pediatr. , vol.135 , pp. 379-383
    • De Lonlay, P.1    Cuer, M.2    Vuillaumier-Barrot, S.3
  • 8
    • 0027420362 scopus 로고
    • Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome
    • R. Weksberg, D.R. Shen, and Y.L. Fei Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome Nat. Genet. 5 1993 143 150
    • (1993) Nat. Genet. , vol.5 , pp. 143-150
    • Weksberg, R.1    Shen, D.R.2    Fei, Y.L.3
  • 9
    • 0022910322 scopus 로고
    • Wiedemann-Beckwith syndrome: Presentation of clinical and cytogenetic data on 22 new cases and review of the literature
    • M.J. Pettenati, J.L. Haines, and R.R. Higgins Wiedemann-Beckwith syndrome: presentation of clinical and cytogenetic data on 22 new cases and review of the literature Hum. Genet. 74 1986 143 154
    • (1986) Hum. Genet. , vol.74 , pp. 143-154
    • Pettenati, M.J.1    Haines, J.L.2    Higgins, R.R.3
  • 10
    • 18544384537 scopus 로고    scopus 로고
    • Haploinsufficiency of NSD1 causes Sotos syndrome
    • N. Kurotaki, K. Imaizumi, and N. Harada Haploinsufficiency of NSD1 causes Sotos syndrome Nat. Genet. 30 2002 365 366
    • (2002) Nat. Genet. , vol.30 , pp. 365-366
    • Kurotaki, N.1    Imaizumi, K.2    Harada, N.3
  • 11
    • 0035093617 scopus 로고    scopus 로고
    • Two patients with Kabuki syndrome presenting with endocrine problems
    • A. Bereket, S. Turan, and G. Alper Two patients with Kabuki syndrome presenting with endocrine problems J. Pediatr. Endocrinol. Metab. 14 2001 215 220
    • (2001) J. Pediatr. Endocrinol. Metab. , vol.14 , pp. 215-220
    • Bereket, A.1    Turan, S.2    Alper, G.3
  • 12
    • 27644549305 scopus 로고    scopus 로고
    • Factitious hyperinsulinism leading to pancreatectomy: Severe forms of Munchausen syndrome by proxy
    • I. Giurgea, T. Ulinski, and G. Touati Factitious hyperinsulinism leading to pancreatectomy: severe forms of Munchausen syndrome by proxy Pediatrics 116 2005 e145 e148
    • (2005) Pediatrics , vol.116
    • Giurgea, I.1    Ulinski, T.2    Touati, G.3
  • 13
    • 0017172436 scopus 로고
    • Transient hepatomegaly and hypoglycemia. a consequence of malicious insulin administration
    • R. Dershewitz, B. Vestal, and N.K. Maclaren Transient hepatomegaly and hypoglycemia. A consequence of malicious insulin administration Am. J. Dis. Child. 130 1976 998 999
    • (1976) Am. J. Dis. Child. , vol.130 , pp. 998-999
    • Dershewitz, R.1    Vestal, B.2    MacLaren, N.K.3
  • 14
    • 0031782335 scopus 로고    scopus 로고
    • Neonatal hyperinsulinemic hypoglycemia: Heterogeneity of the syndrome and keys for differential diagnosis
    • C. Sempoux, Y. Guiot, and A. Lefevre Neonatal hyperinsulinemic hypoglycemia: heterogeneity of the syndrome and keys for differential diagnosis J. Clin. Endocrinol. Metab. 83 1998 1455 1461
    • (1998) J. Clin. Endocrinol. Metab. , vol.83 , pp. 1455-1461
    • Sempoux, C.1    Guiot, Y.2    Lefevre, A.3
  • 15
    • 0021320297 scopus 로고
    • The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: Deficiency of pancreatic D cells or hyperactivity of B cells?
    • J. Rahier, K. Falt, and H. Muntefering The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells? Diabetologia 26 1984 282 289
    • (1984) Diabetologia , vol.26 , pp. 282-289
    • Rahier, J.1    Falt, K.2    Muntefering, H.3
  • 16
    • 0031936418 scopus 로고    scopus 로고
    • Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: The pathologist's role
    • J. Rahier, C. Sempoux, and J.C. Fournet Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role Histopathology 32 1998 15 19
    • (1998) Histopathology , vol.32 , pp. 15-19
    • Rahier, J.1    Sempoux, C.2    Fournet, J.C.3
  • 17
    • 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
    • P. de Lonlay, J.C. Fournet, and J. Rahier 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. 100 1997 802 807
    • (1997) J. Clin. Invest. , vol.100 , pp. 802-807
    • De Lonlay, P.1    Fournet, J.C.2    Rahier, J.3
  • 18
    • 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
    • V. Verkarre, J.C. Fournet, and P. de Lonlay 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. 102 1998 1286 1291
    • (1998) J. Clin. Invest. , vol.102 , pp. 1286-1291
    • Verkarre, V.1    Fournet, J.C.2    De Lonlay, P.3
  • 19
    • 0347359228 scopus 로고    scopus 로고
    • Hyperinsulinism in infancy: From basic science to clinical disease
    • M.J. Dunne, K.E. Cosgrove, and R.M. Shepherd Hyperinsulinism in infancy: from basic science to clinical disease Physiol. Rev. 84 2004 239 275
    • (2004) Physiol. Rev. , vol.84 , pp. 239-275
    • Dunne, M.J.1    Cosgrove, K.E.2    Shepherd, R.M.3
  • 20
    • 0029021696 scopus 로고
    • Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy
    • P.M. Thomas, G.J. Cote, and N. Wohllk Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy Science 268 1995 426 429
    • (1995) Science , vol.268 , pp. 426-429
    • Thomas, P.M.1    Cote, G.J.2    Wohllk, N.3
  • 21
    • 0029658788 scopus 로고    scopus 로고
    • Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy
    • C. Kane, R.M. Shepherd, and P.E. Squires Loss of functional KATP channels in pancreatic beta-cells causes persistent hyperinsulinemic hypoglycemia of infancy Nat. Med. 2 1996 1344 1347
    • (1996) Nat. Med. , vol.2 , pp. 1344-1347
    • Kane, C.1    Shepherd, R.M.2    Squires, P.E.3
  • 22
    • 0029836983 scopus 로고    scopus 로고
    • Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy
    • P. Thomas, Y. Ye, and E. Lightner Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy Hum. Mol. Genet. 5 1996 1809 1812
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1809-1812
    • Thomas, P.1    Ye, Y.2    Lightner, E.3
  • 23
    • 0029658241 scopus 로고    scopus 로고
    • Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
    • A. Nestorowicz, B.A. Wilson, and K.P. Schoor Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews Hum. Mol. Genet. 5 1996 1813 1822
    • (1996) Hum. Mol. Genet. , vol.5 , pp. 1813-1822
    • Nestorowicz, A.1    Wilson, B.A.2    Schoor, K.P.3
  • 24
    • 15644367096 scopus 로고    scopus 로고
    • A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism
    • A. Nestorowicz, N. Inagaki, and T. Gonoi A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism Diabetes 46 1997 1743 1748
    • (1997) Diabetes , vol.46 , pp. 1743-1748
    • Nestorowicz, A.1    Inagaki, N.2    Gonoi, T.3
  • 25
    • 0034902277 scopus 로고    scopus 로고
    • Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion
    • P.T. Clayton, S. Eaton, and A. Aynsley-Green Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion J. Clin. Invest. 108 2001 457 465
    • (2001) J. Clin. Invest. , vol.108 , pp. 457-465
    • Clayton, P.T.1    Eaton, S.2    Aynsley-Green, A.3
  • 26
    • 0030936044 scopus 로고    scopus 로고
    • An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus
    • A. Kukuvitis, C. Deal, and L. Arbour An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus J. Clin. Endocrinol. Metab. 82 1997 1192 1194
    • (1997) J. Clin. Endocrinol. Metab. , vol.82 , pp. 1192-1194
    • Kukuvitis, A.1    Deal, C.2    Arbour, L.3
  • 27
    • 0037464795 scopus 로고    scopus 로고
    • A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1
    • H. Huopio, T. Otonkoski, and I. Vauhkonen A new subtype of autosomal dominant diabetes attributable to a mutation in the gene for sulfonylurea receptor 1 Lancet 361 2003 301 307
    • (2003) Lancet , vol.361 , pp. 301-307
    • Huopio, H.1    Otonkoski, T.2    Vauhkonen, I.3
  • 28
    • 0032493123 scopus 로고    scopus 로고
    • Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene
    • C.A. Stanley, Y.K. Lieu, and B.Y. Hsu Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene N. Engl. J. Med. 338 1998 1352 1357
    • (1998) N. Engl. J. Med. , vol.338 , pp. 1352-1357
    • Stanley, C.A.1    Lieu, Y.K.2    Hsu, B.Y.3
  • 29
    • 0029808377 scopus 로고    scopus 로고
    • Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia
    • E. Zammarchi, L. Filippi, and E. Novembre Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia Metabolism 45 1996 957 960
    • (1996) Metabolism , vol.45 , pp. 957-960
    • Zammarchi, E.1    Filippi, L.2    Novembre, E.3
  • 30
    • 0032556969 scopus 로고    scopus 로고
    • Familial hyperinsulinism caused by an activating glucokinase mutation
    • B. Glaser, P. Kesavan, and M. Heyman Familial hyperinsulinism caused by an activating glucokinase mutation N. Engl. J. Med. 338 1998 226 230
    • (1998) N. Engl. J. Med. , vol.338 , pp. 226-230
    • Glaser, B.1    Kesavan, P.2    Heyman, M.3
  • 31
    • 0037221769 scopus 로고    scopus 로고
    • Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release
    • T. Otonkoski, N. Kaminen, and J. Ustinov Physical exercise-induced hyperinsulinemic hypoglycemia is an autosomal-dominant trait characterized by abnormal pyruvate-induced insulin release Diabetes 52 2003 199 204
    • (2003) Diabetes , vol.52 , pp. 199-204
    • Otonkoski, T.1    Kaminen, N.2    Ustinov, J.3
  • 32
    • 2542610014 scopus 로고    scopus 로고
    • A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene
    • K. Hojlund, T. Hansen, and M. Lajer A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene Diabetes 53 2004 1592 1598
    • (2004) Diabetes , vol.53 , pp. 1592-1598
    • Hojlund, K.1    Hansen, T.2    Lajer, M.3
  • 33
    • 0036895578 scopus 로고    scopus 로고
    • The common single nucleotide polymorphism E23K in K(IR)6.2 sensitizes pancreatic beta-cell ATP-sensitive potassium channels toward activation through nucleoside diphosphates
    • C. Schwanstecher, B. Neugebauer, and M. Schulz The common single nucleotide polymorphism E23K in K(IR)6.2 sensitizes pancreatic beta-cell ATP-sensitive potassium channels toward activation through nucleoside diphosphates Diabetes 51 Suppl 3 2002 S363 S367
    • (2002) Diabetes , vol.51 , Issue.3 SUPPL.
    • Schwanstecher, C.1    Neugebauer, B.2    Schulz, M.3
  • 34
    • 10644233000 scopus 로고    scopus 로고
    • Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features
    • P. Proks, J.F. Antcliff, and J. Lippiat Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features Proc. Natl. Acad. Sci. USA 101 2004 17539 17544
    • (2004) Proc. Natl. Acad. Sci. USA , vol.101 , pp. 17539-17544
    • Proks, P.1    Antcliff, J.F.2    Lippiat, J.3
  • 35
    • 0036534464 scopus 로고    scopus 로고
    • Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations
    • J. Fang, B.Y. Hsu, and C.M. MacMullen Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations Biochem. J. 363 2002 81 87
    • (2002) Biochem. J. , vol.363 , pp. 81-87
    • Fang, J.1    Hsu, B.Y.2    MacMullen, C.M.3
  • 36
    • 14844302859 scopus 로고    scopus 로고
    • Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations
    • D.M. Raizen, A. Brooks-Kayal, and L. Steinkrauss Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations J. Pediatr. 146 2005 388 394
    • (2005) J. Pediatr. , vol.146 , pp. 388-394
    • Raizen, D.M.1    Brooks-Kayal, A.2    Steinkrauss, L.3
  • 38
    • 0018906219 scopus 로고
    • Glycemic response to glucagon during fasting hypoglycemia: An aid in the diagnosis of hyperinsulinism
    • D.N. Finegold, C.A. Stanley, and L. Baker Glycemic response to glucagon during fasting hypoglycemia: an aid in the diagnosis of hyperinsulinism J. Pediatr. 96 1980 257 259
    • (1980) J. Pediatr. , vol.96 , pp. 257-259
    • Finegold, D.N.1    Stanley, C.A.2    Baker, L.3
  • 40
    • 0029098644 scopus 로고
    • Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases
    • J. Dubois, F. Brunelle, and G. Touati Hyperinsulinism in children: diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases Pediatr. Radiol. 25 1995 512 516
    • (1995) Pediatr. Radiol. , vol.25 , pp. 512-516
    • Dubois, J.1    Brunelle, F.2    Touati, G.3
  • 41
    • 19644398630 scopus 로고    scopus 로고
    • Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-Dopa
    • M.J. Ribeiro, P. De Lonlay, and T. Delzescaux Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-Dopa J. Nucl. Med. 46 2005 560 566
    • (2005) J. Nucl. Med. , vol.46 , pp. 560-566
    • Ribeiro, M.J.1    De Lonlay, P.2    Delzescaux, T.3
  • 42
    • 12144291344 scopus 로고    scopus 로고
    • The surgical management of congenital hyperinsulinemic hypoglycemia in infancy
    • C.N. Fekete, P. de Lonlay, and F. Jaubert The surgical management of congenital hyperinsulinemic hypoglycemia in infancy J. Pediatr. Surg. 39 2004 267 269
    • (2004) J. Pediatr. Surg. , vol.39 , pp. 267-269
    • Fekete, C.N.1    De Lonlay, P.2    Jaubert, F.3
  • 44
    • 0027374336 scopus 로고
    • Short-and long-term use of octreotide in the treatment of congenital hyperinsulinism
    • P.S. Thornton, C.A. Alter, and L.E. Katz Short-and long-term use of octreotide in the treatment of congenital hyperinsulinism J. Pediatr. 123 1993 637 643
    • (1993) J. Pediatr. , vol.123 , pp. 637-643
    • Thornton, P.S.1    Alter, C.A.2    Katz, L.E.3
  • 45
    • 0033653702 scopus 로고    scopus 로고
    • Management of hyperinsulinism in infancy and childhood
    • K. Hussain, and A. Aynsley-Green Management of hyperinsulinism in infancy and childhood Ann. Med. 32 2000 544 551
    • (2000) Ann. Med. , vol.32 , pp. 544-551
    • Hussain, K.1    Aynsley-Green, A.2
  • 46
    • 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
    • G. Leibowitz, B. Glaser, and A.A. Higazi 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. 80 1995 386 392
    • (1995) J. Clin. Endocrinol. Metab. , vol.80 , pp. 386-392
    • Leibowitz, G.1    Glaser, B.2    Higazi, A.A.3
  • 47
    • 0036135191 scopus 로고    scopus 로고
    • Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. a series of 175 cases
    • P. de Lonlay, J.C. Fournet, and G. Touati Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases Eur. J. Pediatr. 161 2002 37 48
    • (2002) Eur. J. Pediatr. , vol.161 , pp. 37-48
    • De Lonlay, P.1    Fournet, J.C.2    Touati, G.3
  • 48
    • 0035120388 scopus 로고    scopus 로고
    • Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
    • F. Menni, P. de Lonlay, and C. Sevin Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia Pediatrics 107 2001 476 479
    • (2001) Pediatrics , vol.107 , pp. 476-479
    • Menni, F.1    De Lonlay, P.2    Sevin, C.3


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