Enzyme Replacement Therapy for the Sphingolipidoses
- 1 January 1976
- book chapter
- Published by Springer Nature
- Vol. 68, 523-532
- https://doi.org/10.1007/978-1-4684-7735-1_34
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The Lipid Storage Diseases: New Concepts and ControlAnnals of Internal Medicine, 1975
- The chemistry and control of hereditary lipid diseasesChemistry and Physics of Lipids, 1974
- Replacement Therapy for Inherited Enzyme DeficiencyNew England Journal of Medicine, 1974
- Replacement Therapy for Inherited Enzyme DeficiencyNew England Journal of Medicine, 1973
- [116] β-Hexosaminidase A from human placentaPublished by Elsevier ,1972
- [115] Ceramide trihexosidase from human placentaPublished by Elsevier ,1972
- Demonstration of a deficiency of glucocerebroside-cleaving enzyme in Gaucher's disease.Journal of Clinical Investigation, 1966
- The metabolism of sphingomyelin. II. Evidence of an enzymatic deficiency in Niemann-Pick diseae.Proceedings of the National Academy of Sciences, 1966
- Evidence for the genetic block in metachromatic leucodystrophy (ML)Biochemical and Biophysical Research Communications, 1965
- Metabolism of glucocerebrosides II. Evidence of an enzymatic deficiency in Gaucher's diseaseBiochemical and Biophysical Research Communications, 1965