Galactose intolerance in individuals with double heterozygosity for Duarte variant and galactosemia
- 1 May 1982
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 100 (5) , 704-709
- https://doi.org/10.1016/s0022-3476(82)80568-4
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Significance of the duarte/classical galactosemia genetic compoundThe Journal of Pediatrics, 1979
- Newborn screening for galactosemia and other galactose metabolic defectsThe Journal of Pediatrics, 1978
- Galactose-1-phosphate uridyl transferase deficiency due to Duarte/galactosemia combined variation: Clinical and biochemical studiesThe Journal of Pediatrics, 1978
- Estimation of galactose-1-phosphate in erythrocytes: A rapid and simple enzymatic methodClinica Chimica Acta; International Journal of Clinical Chemistry, 1969
- Studies of lactose absorption in patients with galactosemiaThe Journal of Pediatrics, 1967
- Electrophoretic Variation of Galactose-1-Phosphate UridyltransferaseScience, 1966
- Bestimmung der Galaktose-1-Phosphat-Uridyltransferase im Capillarblut bei der GalaktosämieKlinische Wochenschrift, 1965
- The Value of Galactose Phosphate Determinations in the treatment of GalactosaemiaArchives of Disease in Childhood, 1960
- Galactose metabolism and galactosemiaThe American Journal of Medicine, 1959
- Some disturbances of erythrocyte metabolism in galactosaemiaBiochemical Journal, 1956