Inborn errors of carbohydrate metabolism

Best Practice and Research: Clinical Gastroenterology

Volumn 24, Issue 5, 2010, Pages 607-618

  Mayatepek, Ertan ^a   Hoffmann, Björn ^a   Meissner, Thomas ^a  

^a UNIVERSITY HOSPITAL DÜSSELDORF   (Germany)

Author keywords

Classical galactosaemia; Fructose 1,6 bisphosphate deficiency; Glycogen storage disease; Hepatomegaly; Hereditary fructose intolerance; Hypoglycaemia; Liver adenoma

Indexed keywords

DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; FRUCTOSE 1,6 BISPHOSPHATE; GRANULOCYTE COLONY STIMULATING FACTOR; MESALAZINE; STARCH;

ANTIBIOTIC PROPHYLAXIS; ARTIFICIAL MILK; CLINICAL FEATURE; DIET; DIET THERAPY; DISORDERS OF CARBOHYDRATE METABOLISM; DNA DETERMINATION; ENTERITIS; FRUCTOSE 1,6 BISPHOSPHATE DEFICIENCY; FRUCTOSE METABOLISM; FRUCTOSURIA; GALACTOSEMIA; GENETICS; GLYCOGEN STORAGE DISEASE; HEPATOMEGALY; HEREDITARY FRUCTOSE INTOLERANCE; HIGH RISK PATIENT; HUMAN; HYPOGLYCEMIA; KIDNEY FAILURE; LIVER CIRRHOSIS; LIVER TRANSPLANTATION; LOW DRUG DOSE; MUTATION; NEUTROPENIA; NEWBORN SCREENING; PROGNOSIS; QUALITY OF LIFE; REVIEW; TUBE FEEDING;

EID: 77958101342     PISSN: 15216918     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bpg.2010.07.012     Document Type: Article

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