NEUROCHEMISTRY OF THE MUCOPOLYSACCHARIDOSES: BRAIN GLYCOSAMINOGLYCANS IN NORMALS AND FOUR TYPES OF MUCOPOLYSACCHARIDOSES
- 1 May 1976
- journal article
- research article
- Published by Wiley in Journal of Neurochemistry
- Vol. 26 (5), 901-908
- https://doi.org/10.1111/j.1471-4159.1976.tb06471.x
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Chloride ions cancel out inhibition of β-galactosidase activity by acid mucopolyaccharidesNature, 1975
- Sanfilippo A Syndrome SULFAMIDASE DEFICIENCY IN CULTURED SKIN FIBROBLASTS AND LIVERJournal of Clinical Investigation, 1974
- Hunter's syndrome: A deficiency of L-idurono-sulfate sulfataseBiochemical and Biophysical Research Communications, 1973
- Hurler's syndrome, an a-L-iduronidase deficiencyBiochemical and Biophysical Research Communications, 1972
- L-iduronidase in cultured human fibroblasts and liverBiochemical and Biophysical Research Communications, 1971
- Optical rotatory dispersion of mucopolysaccharides IV. Optical rotatory dispersion and circular dichroism of glycosaminoglycans and heparan sulfate fractions from the urine of patients with mucopolysaccharidosis (Hurler Syndrome)Biochimica et Biophysica Acta (BBA) - General Subjects, 1970
- ISOLATION AND CHARACTERIZATION OF GLYCOSAMINOGLYCANS IN HUMAN BRAIN OF DIFFERENT AGE GROUPSJournal of Neurochemistry, 1968
- Chemical studies in gargoylism.Archives of Disease in Childhood, 1967
- Hurler's syndromeArthritis & Rheumatism, 1961
- Gargoylism – A mucopolysaccharidosisScandinavian Journal of Clinical and Laboratory Investigation, 1951