Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome.
Brivet, M
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome. [electronic resource] - Pediatric research Feb 1983 - 157-61 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0031-3998
10.1203/00006450-198302000-00015 doi
Child, Preschool
Erythrocytes--metabolism
Fanconi Syndrome--complications
Female
Galactose--metabolism
Glucagon
Glucose--metabolism
Glycogen Storage Disease--complications
Glycolysis
Humans
In Vitro Techniques
Kidney--metabolism
Liver--metabolism
Liver Function Tests
Oxidation-Reduction
Defective galactose oxidation in a patient with glycogen storage disease and Fanconi syndrome. [electronic resource] - Pediatric research Feb 1983 - 157-61 p. digital
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
0031-3998
10.1203/00006450-198302000-00015 doi
Child, Preschool
Erythrocytes--metabolism
Fanconi Syndrome--complications
Female
Galactose--metabolism
Glucagon
Glucose--metabolism
Glycogen Storage Disease--complications
Glycolysis
Humans
In Vitro Techniques
Kidney--metabolism
Liver--metabolism
Liver Function Tests
Oxidation-Reduction