Hypoketonuric 3-hydroxydicarboxylic aciduria in five patients with glycogen storage disease

Journal of Inherited Metabolic Disease

Volumn 20, Issue 3, 1997, Pages 407-410

  Mize, C E ^a,b   Waber, L J ^b   Anderson, T ^b   Bennett, M J ^b  

^a UNIVERSITY OF TEXAS SOUTHWESTERN MEDICAL CENTER   (United States)

^b UNIVERSITY OF TEXAS AT DALLAS   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DICARBOXYLIC ACID DERIVATIVE; LONG CHAIN FATTY ACID;

ACIDURIA; CONFERENCE PAPER; FATTY ACID OXIDATION; GLYCOGEN STORAGE DISEASE; HUMAN; HYPOGLYCEMIA; URINALYSIS;

CELLS, CULTURED; CHILD, PRESCHOOL; CREATININE; DICARBOXYLIC ACIDS; FATTY ACIDS; FEMALE; FIBROBLASTS; GAS CHROMATOGRAPHY-MASS SPECTROMETRY; GLYCOGEN STORAGE DISEASE; HUMANS; INFANT; LIVER; MALE; OXIDATION-REDUCTION;

EID: 0030808289     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005354701187     Document Type: Conference Paper

References (12)

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