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Volumn 7, Issue 1, 2002, Pages 17-26

Management and emergency treatments of neonates with a suspicion of inborn errors of metabolism

Author keywords

Fatty acid oxidation defects; Galactosaemia; Gluconeogenesis defects; Glycogen storage diseases; Hyperammonaemia; Ketoacidosis; Neoanatal hypoglycaemias; Organic acidurias; Tyrosinaemia type I; Urea cycle defects

Indexed keywords

BIOTIN; FOLIC ACID; PYRIDOXINE;

EID: 0036303789     PISSN: 10842756     EISSN: None     Source Type: Journal    
DOI: 10.1053/siny.2001.0084     Document Type: Article
Times cited : (50)

References (30)
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    • Burton, B.K.1
  • 4
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    • Comparison of exchange transfusion, peritoneal dialysis, and hemodialysis for the treatment of hyperammonemia in an anuric newborn infant
    • (1979) J Pediatr , vol.95 , pp. 67-70
    • Donn, S.M.1    Swartz, R.D.2    Thoene, J.G.3
  • 9
    • 0028057633 scopus 로고
    • Removal of branched-chain amino acids by peritoneal dialysis, continuous arteriovenous hemofiltration, and continuous arteriovenous hemodialysis in rabbits: Implications for maple syrup urine disease treatment
    • (1994) Pediatr Res , vol.35 , pp. 357-361
    • Gouyon, J.B.1    Desgres, J.2    Mousson, C.3
  • 27
    • 0021673226 scopus 로고
    • Arginine, an indispensable aminoacid for patients with inborn errors of urea synthesis
    • (1984) J Clin Invest , vol.74 , pp. 2144-2148
    • Brusilow, S.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.