Publisher
Springer Berlin Heidelberg
Reference41 articles.
1. Gitzelmann R, Hansen RG (1980) Galactose metabolism, hereditary defects and their clinical significance. In: Burman D, Holton JB, Pennock CA (eds) Inherited disorders of carbohydrate metabolism. MTP, Lancaster, pp 61–101
2. Segal S, Berry GT (1995) Disorders of galactose metabolism. In: Scriver CR, Beaudet AL, Sly WS, Valle D (eds) The metabolic and molecular basis of inherited disease, 7th edn. McGraw-Hill, New York, pp 967–1000
3. Gitzelmann R, Steinmann B (1984) Galactosemia: how does long-term treatment change the outcome? Enzyme 32: 37–46
4. Gitzelmann R (1980) Newborn screening for inherited disorders of galactose metabolism. In: Bickel H, Guthrie R, Hammersen G (eds) Neonatal screening for inborn errors of metabolism. Springer, Berlin Heidelberg New York, pp 67–79
5. Beutler E, Paniker NV, Trinidad F (1971) The assay of red cell galactokinase. Biochem Med 5: 325–332
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