A PATIENT WITH HEREDITARY GALACTOKINASE DEFICIENCY
- 1 November 1970
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 59 (6), 669-675
- https://doi.org/10.1111/j.1651-2227.1970.tb17703.x
Abstract
No abstract availableKeywords
This publication has 21 references indexed in Scilit:
- A PATIENT WITH HEREDITARY GALACTOSEMIA STUDIED WITH A SCREENING METHOD FOR GALACTOSE IN URINEActa Paediatrica, 1969
- Test Paper for Galactose in UrineScandinavian Journal of Clinical and Laboratory Investigation, 1968
- DISORDERS OF CARBOHYDRATE METABOLISM IN INFANCYThe American Journal of the Medical Sciences, 1966
- DEFICIENCY OF ERYTHROCYTE GALACTOKINASE IN A PATIENT WITH GALACTOSE DIABETESThe Lancet, 1965
- The distribution of galactitol in tissues of rats fed galactoseBiochemical and Biophysical Research Communications, 1965
- L'aldose-réductaseBiochimica et Biophysica Acta, 1959
- IDIOSYNCRASY TO FRUCTOSEThe Lancet, 1956
- Congenital Galactosemia, a Single Enzymatic Block in Galactose MetabolismScience, 1956
- Galactosemia, a congenital defect in a nucleotide transferaseBiochimica et Biophysica Acta, 1956
- Levulose im Harn eines DiabetikersDeutsche Medizinische Wochenschrift (1946), 1876