Myopathy due to glycogen storage disease
- 1 June 1983
- journal article
- research article
- Published by Elsevier in Experimental and Molecular Pathology
- Vol. 38 (3) , 405-420
- https://doi.org/10.1016/0014-4800(83)90080-1
Abstract
No abstract availableThis publication has 27 references indexed in Scilit:
- Clinical and Biochemical Findings Before and After Portacaval Shunt in a Girl with Type Ib Glycogen Storage DiseasePediatric Research, 1981
- Lysosomal glycogen storage disease with normal acid maltaseNeurology, 1981
- PHYSICAL-CHEMICAL PROPERTIES OF GLYCOGEN EXTRACTED FROM LIVER OF TYPE II GLYCOGENOSISACTA HISTOCHEMICA ET CYTOCHEMICA, 1979
- Fatal infantile form of muscle phosphorylase deficiencyNeurology, 1978
- The spectrum and diagnosis of acid maltase deficiencyNeurology, 1973
- Type II glycogenosis: Biochemical and electron microscopic studyThe American Journal of Medicine, 1968
- The Determination of Amylo-1,6-GlucosidaseEuropean Journal of Biochemistry, 1967
- Glycogen Storage Disease, Types II, III, VIII, and IXAmerican Journal of Diseases of Children, 1966
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963
- HISTOCHEMICAL METHODS FOR ACID PHOSPHATASE USING HEXAZONIUM PARAROSANILIN AS COUPLERJournal of Histochemistry & Cytochemistry, 1962