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. 1963 Feb;26(1):60–68. doi: 10.1136/jnnp.26.1.60

Skeletal muscle glycogenosis: an investigation of two dissimilar cases1

William H S Thomson 1,2,3,2, John C Maclaurin 1,2,3, John W Prineas 1,2,3
PMCID: PMC495536  PMID: 13981250

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. AEBI U., RICHTERICH R., COLOMBO J. P., ROSSI E. Progressive muscular dystrophy. II. Biochemical identification of the carrier state in the recessive sex-linked juvennile (Duchenne) type by serum creatine-phosphokinase determinations. Epilepsia. 1961;1:61–74. [PubMed] [Google Scholar]
  2. ANDERSEN D. H. Familial cirrhosis of the liver with storage of abnormal glycogen. Lab Invest. 1956 Jan-Feb;5(1):11–20. [PubMed] [Google Scholar]
  3. CHO A. K., HASLETT W. L., JENDEN D. J. A titrimetric method for the determination of creating phosphokinase. Biochem J. 1960 Apr;75:115–119. doi: 10.1042/bj0750115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DI SANT'AGNESE P. A., ANDERSEN D. H., METCALF K. M. Glycogen storage disease of the muscles. Report of a case with unusual features. J Pediatr. 1962 Sep;61:438–442. doi: 10.1016/s0022-3476(62)80375-8. [DOI] [PubMed] [Google Scholar]
  5. DI SANT'AGNESE P. A. Diseases of glycogen storage with special reference to the cardiac type of generalized glycogenosis. Ann N Y Acad Sci. 1959 Feb 6;72(12):439–450. doi: 10.1111/j.1749-6632.1959.tb44172.x. [DOI] [PubMed] [Google Scholar]
  6. ILLINGWORTH B., CORI G. T., CORI C. F. Amylo-1, 6-glucosidase in muscle tissue in generalized glycogen storage disease. J Biol Chem. 1956 Jan;218(1):123–129. [PubMed] [Google Scholar]
  7. MANNERS D. J. The molecular structure of glycogens. Adv Carbohydr Chem. 1957;12:261–298. doi: 10.1016/s0096-5332(08)60210-6. [DOI] [PubMed] [Google Scholar]
  8. MELLICK R. S., MAHLER R. F., HUGHES B. P. McArdle's syndrome: phosphorylase-deficient myopathy. Lancet. 1962 May 19;1(7238):1045–1048. doi: 10.1016/s0140-6736(62)92145-1. [DOI] [PubMed] [Google Scholar]
  9. PEARSON C. M., RIMER D. G. Evidence for direct utilization of fructose in working muscle in man. Proc Soc Exp Biol Med. 1959 Apr;100(4):671–672. doi: 10.3181/00379727-100-24739. [DOI] [PubMed] [Google Scholar]
  10. PEARSON C. M., RIMER D. G., MOMMAERTS W. F. A metabolic myopathy due to absence of muscle phosphorylase. Am J Med. 1961 Apr;30:502–517. doi: 10.1016/0002-9343(61)90075-4. [DOI] [PubMed] [Google Scholar]
  11. REITMAN S., FRANKEL S. A colorimetric method for the determination of serum glutamic oxalacetic and glutamic pyruvic transaminases. Am J Clin Pathol. 1957 Jul;28(1):56–63. doi: 10.1093/ajcp/28.1.56. [DOI] [PubMed] [Google Scholar]
  12. SCHMID R., HAMMAKER L. Hereditary absence of muscle phosphorylase (McArdle's syndrome). N Engl J Med. 1961 Feb 2;264:223–225. doi: 10.1056/NEJM196102022640504. [DOI] [PubMed] [Google Scholar]
  13. SCHMID R., MAHLER R. Chronic progressive myopathy with myoglobinuria: demonstration of a glycogenolytic defect in the muscle. J Clin Invest. 1959 Nov;38:2044–2058. doi: 10.1172/JCI103983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. SLATER E. C. Spectrophotometric determination of fructose-1:6-diphosphate, hexosemonophosphates, adenosinetriphosphate and adenosinediphosphate. Biochem J. 1953 Jan;53(1):157–167. doi: 10.1042/bj0530157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. STETTEN D., Jr, STETTEN M. R. Glycogen metabolism. Physiol Rev. 1960 Jul;40:505–537. doi: 10.1152/physrev.1960.40.3.505. [DOI] [PubMed] [Google Scholar]
  16. SUTHERLAND E. W., WOSILAIT W. D. The relationship of epinephrine and glucagon to liver phosphorylase. I. Liver phosphorylase; preparation and properties. J Biol Chem. 1956 Jan;218(1):459–468. [PubMed] [Google Scholar]
  17. THOMSON W. A. Sources of error in the biochemical diagnosis of muscular dystrophy. J Neurol Neurosurg Psychiatry. 1962 Aug;25:191–202. doi: 10.1136/jnnp.25.3.191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. THOMSON W. H., LEYBURN P., WALTON J. N. Serum enzyme activity in muscular dystrophy. Br Med J. 1960 Oct 29;2(5208):1276–1281. doi: 10.1136/bmj.2.5208.1276. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. VILLAR-PALASI C., LARNER J. A uridine coenzyme-linked pathway of glycogen synthesis in muscle. Biochim Biophys Acta. 1958 Nov;30(2):449–449. doi: 10.1016/0006-3002(58)90086-6. [DOI] [PubMed] [Google Scholar]

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