A possible unrecognized disease of galactose metabolism
- 1 June 1983
- journal article
- research article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 6 (S2) , 131-132
- https://doi.org/10.1007/bf01810362
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
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- FAMILIAL FANCONI SYNDROME WITH MALABSORPTION AND GALACTOSE INTOLERANCE, NORMAL KINASE AND TRANSFERASE ACTIVITY.Acta Paediatrica, 1981
- Hepatic phosphorylase deficiency: Its differentiation from other hepatic glycogenosesArchives of Disease in Childhood, 1974
- A PATIENT WITH HEREDITARY GALACTOKINASE DEFICIENCYActa Paediatrica, 1970
- AN INTRAVENOUS GALACTOSE TOLERANCE TEST AND ITS USE IN HEPATOBILIARY DISEASES1Acta Medica Scandinavica, 1968
- Hereditary Galactokinase Deficiency, a Newly Recognized Cause of Juvenile Cataracts31Pediatric Research, 1966
- A Clinical and Biochemical Study of Galactosaemia: A Possible Explanation of the Nature of the Biochemical LesionArchives of Disease in Childhood, 1956
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956