Biosynthesis of acid α‐glucosidase in late‐onset forms of glycogenosis type II (Pompe's disease)

α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)

1963 • 847 citations

Biosynthesis of lysosomal enzymes in fibroblasts. Synthesis as precursors of higher molecular weight.

1980 • 809 citations

Lysosomes and storage diseases

1973 • 745 citations

Chloroquine inhibits lysosomal enzyme pinocytosis and enhances lysosomal enzyme secretion by impairing receptor recycling.

1980 • 743 citations

Biosynthesis of lysosomal enzymes in fibroblasts. Phosphorylation of mannose residues.

1980 • 404 citations

Lysosomes and lysosomal storage diseases

1981 • 315 citations

Biochemical, immunological, and cell genetic studies in glycogenosis type II.

1978 • 119 citations

[121] Corrective factors for inborn errors of mucopolysaccharide metabolism

1972 • 104 citations

Rodent and Human Acid α‐Glucosidase

1972 • 81 citations

Enhanced Breakdown of Arylsulfatase A in Multiple Sulfatase Deficiency

1982 • 76 citations

Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts.

1978 • 57 citations

Acid maltase deficiency in non-identical adult twins

1976 • 49 citations

The molecular heterogeneity of purified human liver lysosomal α-Glucosidase (acid α-Glucosidase)

1978 • 42 citations

Use of immobilized antibodies in investigating acid α-glucosidase in urine in relation to Pompe's disease

1979 • 37 citations

Some properties of human liver acid α-glucosidase

1977 • 34 citations

Adult forms of glycogenosis type II

1982 • 31 citations

Late-Onset Acid Maltase Deficiency

1976 • 29 citations