Short-Term Enzyme Replacement in the Murine Model of Sanfilippo Syndrome Type B

Replacement Therapy for Inherited Enzyme Deficiency — Macrophage-Targeted Glucocerebrosidase for Gaucher's Disease

Norman W. Barton, Roscoe O. Brady, James M. Dambrosia et al. · New England Journal of Medicine · 1991 · 1.3K citations · Full text

Life Sciences, Biochemistry, Pharmacotherapy +17

Enzyme Therapy in Type 1 Gaucher Disease: Comparative Efficacy of Mannose-Terminated Glucocerebrosidase from Natural and Recombinant Sources

Gregory A. Grabowski · Annals of Internal Medicine · 1995 · 448 citations

Life Sciences, Biochemistry, Hematology +14

Infusion of α-galactosidase A reduces tissue globotriaosylceramide storage in patients with Fabry disease

Raphael Schiffmann, Gary J. Murray, DA Treco et al. · Proceedings of the National Academy of Sciences · 2000 · 346 citations

Life Sciences, Biochemistry, Pharmacokinetics +17

An electron microscope autoradiographic study of the carbohydrate recognition systems in rat liver. I. Distribution of 125I-ligands among the liver cell types.

A L Hubbard, Glynn Wilson, Gilbert Ashwell et al. · The Journal of Cell Biology · 1979 · 313 citations · Full text

Life Sciences, Biochemistry, Cell Biology +17

Murine mucopolysaccharidosis type VII. Characterization of a mouse with beta-glucuronidase deficiency.

E H Birkenmeier, Muriel T. Davisson, Wesley G. Beamer et al. · Journal of Clinical Investigation · 1989 · 291 citations · Full text

Life Sciences, Genetics, Molecular Biology +12