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Volumn 51, Issue 3, 2009, Pages 409-410

Early neonatal onset carbamoyl-phosphate synthase 1 deficiency treated with continuous hemodiafiltration and early living-related liver transplantation

Author keywords

Carbamoyl phosphate synthase 1 deficiency; Continuous hemodiafiltration; Hyperammonemia; Liver transplantation

Indexed keywords

ALANINE AMINOTRANSFERASE; AMMONIA; ARGININE; ASPARTATE AMINOTRANSFERASE; BENZOIC ACID; CARNITINE; CITRULLINE; GLUCOSE; GLUTAMIC ACID; ORNITHINE; PHENYLACETIC ACID; PROTEIN;

EID: 66549096908     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200X.2009.02831.x     Document Type: Article
Times cited : (5)

References (7)
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  • 2
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  • 4
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    • Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies
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  • 5
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    • Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis
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    • (1999) J. Pediatr. , vol.134 , pp. 268-72
    • Maestri, N.E.1    Clissold, D.2    Brusilow, S.W.3
  • 6
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    • Liver transplantation for the treatment of urea cycle disorders
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    • McBride, K.L.1    Miller, G.2    Carter, S.3    Karpen, S.4    Goss, J.5    Lee, B.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.