Brain sphingolipids in I cell disease (mucolipidosis II)

This publication has 16 references indexed in Scilit:

• Mucopolysaccharidosis: Secondarily Induced Abnormal Distribution of Lysosomal Isoenzymes
  Science, 1973
• A hypothesis for I-cell disease: Defective hydrolases that do not enter lysosomes
  Biochemical and Biophysical Research Communications, 1972
• Clinical, biochemical, and ultrastructural studies in a case of chondrodystrophy presenting the I-cell phenotype in tissue culture
  The Journal of Pediatrics, 1971
• I-cell disease: A clinical picture
  The Journal of Pediatrics, 1971
• I-CELL DISEASE : MULTIPLE LYSOSOMAL-ENZYME DEFECT
  The Lancet, 1971
• Hurler's Syndrome: Deficiency of a Specific Beta Galactosidase Isoenzyme
  Science, 1969
• Lysosomal Acid Hydrolases in the Liver in Gargoylism Deficiency of 4-methylumbelliferyl-β-galactosidase
  Scandinavian Journal of Clinical and Laboratory Investigation, 1968
• Mutant Enzymatic and Cytological Phenotypes in Cultured Human Fibroblasts
  Science, 1967
• A simple and accurate micromethod for quantitative determination of ganglioside patterns
  Life Sciences, 1964
• Use of Butyl Acetate in Determination of Sialic Acid.
  Acta Chemica Scandinavica, 1959