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Volumn 16, Issue 1, 2006, Pages 64-69

Metabolic disease as a cause of chronic liver disease in children

Author keywords

Chronic liver disease; Clinical phenotypes; Glycogen storage diseases; Metabolic liver disease; Neonatal liver disease; Organomegaly

Indexed keywords

CHOLIC ACID; GLUCOSYLCERAMIDASE; HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR; MIGLUSTAT; NITISINONE; PENICILLAMINE; PYRIDOXINE; TRIENTINE; ZINC;

EID: 31544444690     PISSN: 09575839     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cupe.2005.10.001     Document Type: Article
Times cited : (4)

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    • P. Lykavieris, S. van Mil, and D. Cresteil Progressive familial intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation J Hepatol 39 2003 447 452
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    • Lykavieris, P.1    Van Mil, S.2    Cresteil, D.3
  • 4
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    • Neonatal cholestasis
    • P.J. McKiernan Neonatal cholestasis Semin Neonatol 7 2002 153 165
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    • S. Lindstedt, E. Holme, E.A. Lock, O. Hjalmarson, and B. Strandvik Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase Lancet 340 1992 813 817
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.