Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndrome
- 1 May 1976
- journal article
- case report
- Published by Springer Nature in Nature
- Vol. 261 (5558) , 323-325
- https://doi.org/10.1038/261323a0
Abstract
No abstract availableThis publication has 11 references indexed in Scilit:
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- Quantitative Aspects of Pinocytosis and the Intracellular Fate of N-acetyl-α-D-glucosaminidase in Sanfilippo B FibroblastsJournal of Clinical Investigation, 1974
- Sanfilippo Disease Type B: Enzyme Replacement and Metabolic Correction in Cultured FibroblastsScience, 1973
- The Defect in the Hunter Syndrome: Deficiency of Sulfoiduronate SulfataseProceedings of the National Academy of Sciences, 1973
- Mobilization of Glycosaminoglycans by Plasma Infusion in Mucopolysaccharidosis Type III-Two Types of ResponseNature New Biology, 1973
- Hurler's, Hunter's and Morquio's syndromes. A biochemical study in the light of current views of the underlying defectsBiochemical Journal, 1971
- Induced Degradation of Glycosaminoglycans in Hurler's and Hunter's Syndromes by Plasma InfusionProceedings of the National Academy of Sciences, 1971
- THE DEFECT IN HURLER AND HUNTER SYNDROMES, II. DEFICIENCY OF SPECIFIC FACTORS INVOLVED IN MUCOPOLYSACCHARIDE DEGRADATIONProceedings of the National Academy of Sciences, 1969
- The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.Proceedings of the National Academy of Sciences, 1968
- Protein-polysaccharides of pig laryngeal cartilageBiochemical Journal, 1967