Type VI glycogenosis: identification of subgroups-Reference-Cited by-同舟云学术

Type VI glycogenosis: identification of subgroups

Published:1980 Issue: Volume: Page:369-380
ISSN:
Container-title:Inherited Disorders of Carbohydrate Metabolism
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Author:

de Barsy Th.,Lederer B.

Publisher

Springer Netherlands

Link

http://link.springer.com/content/pdf/10.1007/978-94-009-9215-3_21

Reference33 articles.

1. H. G. Hers, (1959). Etude enzymatique sur fragments hepatiques. Applications a la classification des glycogenoses. Rev. Int. Hepat., 9, 35

2. D. W. Stetten Jr, and M. R. Stetten, (1960). Glycogen metabolism. Physiol. Rev., 40, 505

3. W. Stalmans and H. G. Hers, (1975). The stimulation of liver phosphorylaseb by AMP, fluoride and sulfate. A technical note on the specific determination of the a and b forms of liver glycogen phosphorylase. Eur. J. Biochem., 54, 341

4. B. Lederer and W. Stalmans, (1976). Human liver glycogen phosphorylase. Kinetic properties and assay in biopsy specimens. Biochem. J., 159, 689

5. B. Illingworth and D. H. Brown, (1964). Glycogen storage diseases, types III, IV and VI. In W. J. Whelan and M. P. Cameron (eds). Ciba Foundation Symposium: Control of Glycogen Metabolism, pp. 336–353 (Elsevier Publishing Co. Amsterdam)

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1. Diagnosis of glycogen storage disease;Journal of Inherited Metabolic Disease;1990-07

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3. Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscle;European Journal of Pediatrics;1989-10

4. The effect of ethanol on glucose production in phosphorylase b kinase deficiency;Journal of Inherited Metabolic Disease;1989-09

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