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Volumn 39, Issue 2, 2000, Pages 117-119

Factitious hyperinsulinemic hypoglycemia in infancy: Diagnostic pitfalls

Author keywords

[No Author keywords available]

Indexed keywords

DIAZOXIDE; GLUCAGON; HYDROCORTISONE; INSULIN; SOMATOSTATIN;

EID: 0033980864     PISSN: 00099228     EISSN: None     Source Type: Journal    
DOI: 10.1177/000992280003900208     Document Type: Article
Times cited : (9)

References (14)
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  • 2
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    • Transient hepatomegaly and hypoglycemia: A consequence of surreptitious insulin administration
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  • 3
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    • Factitious diabetes mellitus and spontaneous hypoglycemia: Consequences of unrecognized munchausen syndrome by proxy
    • Kovacs CS, Toth EL. Factitious diabetes mellitus and spontaneous hypoglycemia: consequences of unrecognized Munchausen syndrome by proxy. Diabetes Care. 1993;16:1294-1297.
    • (1993) Diabetes Care , vol.16 , pp. 1294-1297
    • Kovacs, C.S.1    Toth, E.L.2
  • 4
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    • Factitious hypoglycemia: A diagnosis by measurement of serum C-peptide immunoreactivity and insulin binding antibodies
    • Scarlett JA, Mako ME, Rubenstein AH, et al. Factitious hypoglycemia: a diagnosis by measurement of serum C-peptide immunoreactivity and insulin binding antibodies. N Engl J Med. 1977;297:1029-1032.
    • (1977) N Engl J Med. , vol.297 , pp. 1029-1032
    • Scarlett, J.A.1    Mako, M.E.2    Rubenstein, A.H.3
  • 5
    • 0027525388 scopus 로고
    • The enigma of persistent hyperinsulinemic hypoglycemia of infancy
    • Daneman D, Ehrlich RM. The enigma of persistent hyperinsulinemic hypoglycemia of infancy [editorial]. J Pediatr. 1993;123:573-575.
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  • 6
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    • Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant
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    • (1998) J Pediatr. , vol.132 , pp. 9-14
    • Thornton, P.S.1    Satin-Smith, M.S.2    Herold, K.3
  • 7
    • 0030029753 scopus 로고    scopus 로고
    • Nesidioblastosis unraveled
    • Milner RDG. Nesidioblastosis unraveled. Arch Dis Child. 1996;74:369-372.
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    • Milner, R.D.G.1
  • 8
    • 0029021696 scopus 로고
    • Mutations in the sulfonylurea receptor gene in familial peristent hyperinsulinemic hypoglycemia of infancy
    • Thomas PM, Cote GJ, Wohlik N, et al. Mutations in the sulfonylurea receptor gene in familial peristent hyperinsulinemic hypoglycemia of infancy. Science: 1995;268:425-429.
    • (1995) Science , vol.268 , pp. 425-429
    • Thomas, P.M.1    Cote, G.J.2    Wohlik, N.3
  • 9
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    • Mutation of the pancreatic inward rectifier Kir6.2 also leads to familal persistent hyperinsulinemic hypoglycemia of infancy
    • Thomas PM, Ye Y, Lightner E. Mutation of the pancreatic inward rectifier Kir6.2 also leads to familal persistent hyperinsulinemic hypoglycemia of infancy. Hum Mol Genet. 1996;5:1809-1812.
    • (1996) Hum Mol Genet. , vol.5 , pp. 1809-1812
    • Thomas, P.M.1    Ye, Y.2    Lightner, E.3
  • 10
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    • Pancreatic histology in hyperinsulinemic hypoglycemia of infancy
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  • 11
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  • 12
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    • Seferian, E.G.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.