Sulphatase Deficiencies
- 1 January 1977
- book chapter
- Published by Springer Nature
Abstract
No abstract availableKeywords
This publication has 64 references indexed in Scilit:
- Enzyme replacement therapy by fibroblast transplantation in a case of Hunter syndromeNature, 1976
- Uridine diphospho-N-acetylgalactosamine-4-sulfate sulfohydrolase activity of human arylsulfatase B and its deficiency in the Maroteaux-Lamy syndromeBiochemical and Biophysical Research Communications, 1975
- The nature of the residual arylsulfatase activity in metachromatic leukodystrophyThe Journal of Pediatrics, 1975
- Deficiency of seminolipid sulphatase activity in brain tissue of metachromatic leucodystrophyJournal of Neurochemistry, 1975
- The Activator of Cerebroside Sulphatase. Purification from Human Liver and Identification as a ProteinHoppe-Seyler´s Zeitschrift Für Physiologische Chemie, 1975
- Expression of the neuron‐specific protein, 14‐3‐2, and steroid sulfatase in neuroblastoma cell hybridsJournal of Cellular Physiology, 1974
- Morquio's syndrome: Deficiency of a chondroitin sulfate N-acetylhexosamine sulfate sulfataseBiochemical and Biophysical Research Communications, 1974
- Maroteaux-lamy disease (mucopolysaccharidosis VI), subtype A: Deficiency of a N-acetylgalactosamine-4-sulfataseBiochemical and Biophysical Research Communications, 1974
- Arylsulfatase B deficiency in maroteaux-lamy syndrome cultured fibroblastsBiochemical and Biophysical Research Communications, 1974
- A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomesBiochemical and Biophysical Research Communications, 1972