Early manifestations of multiple sulfatase deficiency
- 1 January 1984
- journal article
- research article
- Published by Elsevier
- Vol. 104 (4) , 574-578
- https://doi.org/10.1016/s0022-3476(84)80550-8
Abstract
No abstract availableThis publication has 14 references indexed in Scilit:
- Urinary acid mucopolysaccharides in Multiple Sulfatase Deficiency (Mucosulfatidosis)European Journal of Pediatrics, 1979
- Sialidase (α‐N‐acetyl neuraminidase) deficiency: the enzyme defect in an adult with macular cherry‐red spots and myoclonus without dementiaClinical Genetics, 1978
- Increased levels of sialic acid associated with a sialidase deficiency in I-cell disease (mucolipidosis II) fibroblastsBiochemical and Biophysical Research Communications, 1976
- Metachromatic LeukodystrophyArchives of Neurology, 1975
- ENZYMIC STUDIES OF SULPHATASES IN TISSUES OF THE NORMAL HUMAN AND IN METACHROMATIC LEUKODYSTROPHY WITH MULTIPLE SULPHATASE DEFICIENCIES: ARYLSULPHATASES A, B AND C, CEREBROSIDE SULPHATASE, PSYCHOSINE SULPHATASE AND STEROID SULPHATASES1Journal of Neurochemistry, 1974
- Mucolipidosis III (pseudo‐Hurler polydystrophy): Cytological and ultrastructural observations of cultured fibroblast cellsClinical Genetics, 1973
- Analysis of in mucolipidosis II (I-cell disease)Clinica Chimica Acta; International Journal of Clinical Chemistry, 1973
- Studies in Metachromatic LeukodystrophyArchives of Neurology, 1973
- The defect in Hurler's and Hunter's syndromes: faulty degradation of mucopolysaccharide.Proceedings of the National Academy of Sciences, 1968
- Metachromatic Form of Diffuse Cerebral SclerosisArchives of Neurology, 1965