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Biochemical and Molecular Medicine|August 1, 1996
Long-term and high-dose trials of enzyme replacement therapy in the canine model of mucopolysaccharidosis IE D Kakkis, M F McEntee, A Schmidtchen, et al.Proceedings of the National Academy of Sciences of the United States of America|December 10, 1999
Mouse model of Sanfilippo syndrome type B produced by targeted disruption of the gene encoding alpha-N-acetylglucosaminidaseH H Li, W H Yu, N Rozengurt, et al.Journal of Inherited Metabolic Disease|January 1, 1992
Attempted enzyme replacement using human amnion membrane implantations in mucopolysaccharidosesJ Muenzer, E F Neufeld, G Constantopoulos, et al.The New England Journal of Medicine|February 15, 2001
Enzyme-replacement therapy in mucopolysaccharidosis IE D Kakkis, J Muenzer, G E Tiller, et al.American Journal of Medical Genetics|November 1, 1982
Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical studyF R Brown, C W Hall, E F Neufeld, et al.Pediatric Research|March 1, 1982
Nonuniform deficiency of hexosaminidase A in tissues and fluids of two unrelated individualsG H Thomas, S Raghavan, E H Kolodny, et al.Human Mutation|January 1, 1997
Fourteen novel mucopolysaccharidosis IVA producing mutations in GALNS geneS Tomatsu, S Fukuda, A Cooper, et al.Pageof 12