Abstract

1. Senior B, and Loridan L: Studies of liver glycogenoses with particular reference to the metabolism of intravenously administrated glycerol, N Engl J Med 279:958, 1968. 2. Seifter S, Dayton S, Novis B, and Muntwyler E: The estimation of glycogen with the anthrome reagent, Arch Biochem 25:191, 1950. 3. Hers HG, and Van Hoof F: Enzymes of glycogen degradation in biopsy material, Methods Enzymol 8:525, 1966. 4. Baker L, and Winegrad AI: Fasting hypoglycemia and metabolic acidosis associated to deficiency of hepatic fructose1,6-diphosphatase, Lancet 2:13, 1970. 5. Van Hoof F, Hue L, de Barsy T, Jacquemin P, I~evos P, and Hers HG: Glycogen storage diseases, Biochimie 54:745, 1972. 6. Report on decisions at the 1959 meeting of the International Commission on Radiological Protection (I.C.R.P.), Br J Radiol 33:189, 1960. 7. Hers HG: The control of glycogen metabolism in the liver, Ann Rev Biochem 45:167, 1976. 8. Hue L, and Hers HG: The turn-over of (2-~H) glucose. An assay for the diagnosis of type 1 glycogenosis, in Piras R, and Pontis HG, editors: Biochemistry of the glycosidic linkage. An integrated view-PAABS Symposium, New York, 1972, McGraw-Hill Book Company, p 149-173. 9. Munkres KD, and Woodward DA: On genetics of enzyme locational specificity. Proc Natl Acad Sci 55:1217, 1966. 10. Arion WJ, Wallin BK, Lange AJ, and Ballas LM: On the involvement of a glucose-6-phosphate transport system in the function of microsomial glucose-6-phosphatase, Mol Cell Biochem 6:75, 1975. 11. Bialek DS, Sharp HL, Kane WJ, Elders J, and Nordlie RC: Latency of glucose-6-phosphatase (G-6-P) in type IB glycogen storage disease (absr), J PEDIATR 91:938, 1977. 12. Narisawa K, Igarashi Y, Otomo H, and Tada K: A new variant of glycogen storage disease type I probably due to a defect in the glucose-6-phosphate transport system, Biochem Biophys Res Comm 83:1360, 1978.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call