Studies on GM1-gangliosidosis, type II

This publication has 20 references indexed in Scilit:

• Deficiency of α-L-Fucosidase
  Science, 1972
• The electrophoretic separation of human β-galactosidases on cellulose acetate
  Biochemical Medicine, 1971
• Detection of Tay-Sachs disease heterozygotes by assay of hexosaminidase A in serum and leukocytes
  The Journal of Pediatrics, 1971
• Determination of gangliosides, glycoproteins, and glycosaminoglycans in brain tissue
  Clinica Chimica Acta; International Journal of Clinical Chemistry, 1971
• Lysosomal β-galactosidases of rat kidney
  Biochimica et Biophysica Acta (BBA) - Enzymology, 1970
• Hyaluronidase and sulfatase deficiency in Hurler's syndrome
  Biochemical Medicine, 1970
• Generalized Gangliosidosis — GM1 (Landing Disease)
  European Neurology, 1970
• GM1 Gangliosidosis Type II
  European Neurology, 1970
• Thin-layer chromatography as a screening technique for the study of lipids in the central nervous system
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1966
• HISTOCHEMICAL STUDIES IN HURLER'S DISEASE: A NEW METHOD FOR LOCALIZATION OF ACID MUCOPOLYSACCHARIDE, AND AN ANALYSIS OF LEAD ACETATE "FIXATION"
  Journal of Histochemistry & Cytochemistry, 1961