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- BAUDHUIN P., HERS H. G., LOEB H. AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS. Lab Invest. 1964 Sep;13:1139–1152. [PubMed] [Google Scholar]
- BIAVA C. IDENTIFICATION AND STRUCTURAL FORMS OF HUMAN PARTICULATE GLYCOGEN. Lab Invest. 1963 Dec;12:1179–1197. [PubMed] [Google Scholar]
- CLEMENT D. H., GODMAN G. C. Glycogen disease resembling mongolism, cretinism, and amytonia congenita; case report and review of literature. J Pediatr. 1950 Jan;36(1):11-30, illust. doi: 10.1016/s0022-3476(50)80174-9. [DOI] [PubMed] [Google Scholar]
- DI SANT'AGNESE P. A., ANDERSEN D. H., MASON H. H., BAUMAN W. A. Glycogen storage disease of the heart. I. Report of 2 cases in siblings with chemical and pathologic studies. Pediatrics. 1950 Sep;6(3):402–424. [PubMed] [Google Scholar]
- Hug G., Schubert W. K., Shwachman H. Imbalance of liver phosphorylase and accumulation of hepatic glycogen in a girl with progressive disease of the brain. J Pediatr. 1965 Nov;67(5):741–751. doi: 10.1016/s0022-3476(65)80362-6. [DOI] [PubMed] [Google Scholar]
- KAHANA D., TELEM C., STEINITZ K., SOLOMON M. GENERALIZED GLYCOGENOSIS. REPORT OF A CASE WITH DEFICIENCY OF ALPHA GLUCOSIDASE. J Pediatr. 1964 Aug;65:243–251. doi: 10.1016/s0022-3476(64)80526-6. [DOI] [PubMed] [Google Scholar]
- KRIVIT W., POLGLASE W. J., GUNN F. D., TYLER F. H. Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita. Pediatrics. 1953 Aug;12(2):165–177. [PubMed] [Google Scholar]



