Reply
- 30 November 1990
- journal article
- letter
- Published by Elsevier in The Journal of Pediatrics
- Vol. 117 (5), 840-842
- https://doi.org/10.1016/s0022-3476(05)83363-3
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Defective Galactosylation of Proteins in Cultured Skin Fibroblasts from Galactosaemic PatientsAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 1990
- Effect of Uridine on Hepatic Galactose-1-Phosphate UridyltransferaseEnzyme, 1989
- Deficit of uridine diphosphate galactose in galactosaemiaJournal of Inherited Metabolic Disease, 1989
- Altered erythrocyte nucleotide patterns are characteristic of inherited disorders of purine or pyrimidine metabolismClinica Chimica Acta; International Journal of Clinical Chemistry, 1988
- Progressive cerebellar and extrapyramidal motor disturbances in galactosaemic twinsEuropean Journal of Pediatrics, 1986
- Identification of cytidine diphosphodiesters in erythrocytes from a patient with pyrimidine nucleotidase deficiencyBlood, 1984
- A new mass screening method for determining UDP-galactose in blood.The Tohoku Journal of Experimental Medicine, 1983
- Further observations in a case of uridine diphosphate galactose‐4‐epimerase deficiency with a severe clinical presentationJournal of Inherited Metabolic Disease, 1982
- Distribution of Erythrocyte Nucleotides in Pyrimidine 5'-Nucleotidase DeficiencyBritish Journal of Haematology, 1979
- THE NEUROPATHOLOGY OF GALACTOSEMIAJournal of Neuropathology and Experimental Neurology, 1971