Early recognition of metabolic decompensation

Archives of Disease in Childhood

Volumn 76, Issue 6, 1997, Pages 555-556

  Morris, A A M ^a,b   Leonard, J V ^a,b  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b ROYAL VICTORIA INFIRMARY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL MARKER; FATTY ACID; UREA;

CHILD; GLYCOGEN STORAGE DISEASE TYPE 1; HUMAN; INBORN ERROR OF METABOLISM; MAPLE SYRUP URINE DISEASE; METABOLIC ENCEPHALOPATHY; METABOLISM; OXIDATION REDUCTION REACTION; REVIEW;

BIOLOGICAL MARKERS; BRAIN DISEASES, METABOLIC; CHILD; FATTY ACIDS; GLYCOGEN STORAGE DISEASE TYPE I; HUMANS; MAPLE SYRUP URINE DISEASE; METABOLISM, INBORN ERRORS; OXIDATION-REDUCTION; UREA;

EID: 0031160458     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.76.6.555     Document Type: Article

References (3)

1. Dixon MA, Leonard JV. Intercurrent illness in inborn errors of intermediary metabolism. Arch Da Chad 1992;67:1387-91.
2. Fernandes J, Berger R, Smit GP. Lactate as a cerebral metabolic fuel for glucose-6-phosphatase deficient children. PediatrRa 1984;18:335-9.
3. Maestri ME, McGowan KD, Brusilow SW. Plasma glutamine concentration: a guide in the management of urea cycle disorders. J Pediatr 1992;121:259-61.