Galactose Metabolism in a Patient with Hereditary Galactokinase Deficiency
- 1 February 1974
- journal article
- Published by Wiley in European Journal of Clinical Investigation
- Vol. 4 (1) , 79-84
- https://doi.org/10.1111/j.1365-2362.1974.tb00376.x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Galactonic Acid in Galactosemia: Identification in the UrineScience, 1972
- Das Fehlen von Insulinstimulation durch Galactose bei Patienten mit Galactokinase-MangelDiabetologia, 1969
- The oxidation of C14galactose by patients with congenital galactosemia: Evidence for a direct oxidative pathwayThe American Journal of Medicine, 1968
- The metabolic fate of [i−14C]galactitol in mammalian tissueBiochimica et Biophysica Acta (BBA) - General Subjects, 1968
- Galactose Toxicity and Myoinositol Metabolism in the Developing Rat Brain*Biochemistry, 1967
- Galactitol and galactose-1-phosphate in the lens of a galactosemic infantExperimental Eye Research, 1967
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- Galactose Conversion to D-Xylulose: An Alternate Route of Galactose MetabolismScience, 1966
- The metabolism of galactose by patients with congenital galactosemiaThe American Journal of Medicine, 1965
- PROGESTERONE EFFECTS ON GALACTOSE METABOLISM IN PREPUBERTAL PATIENTS WITH CONGENITAL GALACTOSEMIA AND IN RATS MAINTAINED ON HIGH GALACTOSE DIETS*Journal of Clinical Investigation, 1960