Simultaneous absence of α-1,4-glucosidase and α-1,6-glucosidase activities (pH 4) in tissues of children with Type II glycogen storage disease
Data up to Jan 2025
Total Citations Per Year
Abstract
References (12)
α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)
1963 • 847 citations
AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS.
1964 • 249 citations
Tissue fractionation studies. 16. Intracellular distribution and properties of α-glucosidases in rat liver
1963 • 196 citations
Lysosomal α-glucosidase. I. Purification and properties of the rat liver enzyme
1970 • 91 citations
The subcellular distribution of enzymes in type II glycogenosis and the occurrence of an oligo-α-1,4-glucan glucohydrolase in human tissues
1965 • 60 citations
Lysosomal α-glucosidase. II. Kinetics of action of the rat liver enzyme
1970 • 58 citations
A HISTOCHEMICAL AND ELECTRON MICROSCOPIC STUDY OF SKELETAL MUSCLE IN A CASE OF POMPE'S DISEASE (GLYCOGENOSIS II)
1966 • 48 citations
Purification of an acid α-glucosidase by dextran-gel filtration
1967 • 48 citations
Glycogen-Storage Diseases**This review is dedicated to Carl F. Cori on the occasion of his seventieth birthday.: Types I, III, IV, V, VII and Unclassified Glycogenoses
1968 • 46 citations
α-1,4-Glucosidase Activity in Leucocytes from the Family of Two Brothers Who Lack this Enzyme in Muscle
1966 • 39 citations
Further purification and characterization of the acid α-glucosidase
1968 • 36 citations
Cardiac glycogenosis
1966 • 17 citations