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Volumn 16, Issue 1, 2006, Pages 64-69
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Metabolic disease as a cause of chronic liver disease in children
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Author keywords
Chronic liver disease; Clinical phenotypes; Glycogen storage diseases; Metabolic liver disease; Neonatal liver disease; Organomegaly
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Indexed keywords
CHOLIC ACID;
GLUCOSYLCERAMIDASE;
HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE INHIBITOR;
MIGLUSTAT;
NITISINONE;
PENICILLAMINE;
PYRIDOXINE;
TRIENTINE;
ZINC;
ABDOMINAL DISCOMFORT;
ALPHA 1 ANTITRYPSIN DEFICIENCY;
ANEMIA;
BILE ACID SYNTHESIS;
BONE MARROW SUPPRESSION;
CHOLESTASIS;
CHOLESTEROL ESTER STORAGE DISEASE;
CHRONIC LIVER DISEASE;
CLINICAL TRIAL;
DIARRHEA;
DISEASE ASSOCIATION;
DRUG MECHANISM;
FAMILY HISTORY;
FEVER;
GAUCHER DISEASE;
GENETIC COUNSELING;
GLYCOGEN STORAGE DISEASE TYPE 1;
GLYCOGEN STORAGE DISEASE TYPE 3;
GLYCOGEN STORAGE DISEASE TYPE 4;
GLYCOGEN STORAGE DISEASE TYPE 6;
HUMAN;
INTRAHEPATIC CHOLESTASIS;
LABORATORY TEST;
LIVER TRANSPLANTATION;
METABOLIC DISORDER;
NIEMANN PICK DISEASE;
PHENOTYPE;
POSTOPERATIVE COMPLICATION;
PROGNOSIS;
PROTEINURIA;
RASH;
REVIEW;
SKIN DISEASE;
STEATOSIS;
SYSTEMIC LUPUS ERYTHEMATOSUS;
TYROSINEMIA;
WILSON DISEASE;
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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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References (11)
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