Determination of Urinary Sulfatides and Other Lipids by Combination of Reversed-Phase and Thin-Layer Chromatographies

This publication has 24 references indexed in Scilit:

• Pseudodeficiency of arylsulphatase A: Strategy for clarification of genotype in families of subjects with low ASA activity and neurological symptoms
  Journal of Inherited Metabolic Disease, 1995
• Quantitative correlation between the residual activity of β-hexosaminidase A and arylsulfatase A and the severity of the resulting lysosomal storage disease
  Human Genetics, 1992
• Phenotypic Consequences of Low Arylsulfatase A Genotypes (ASAp/ASAp and ASA–/ASAp): Does There Exist an Association with Multiple Sclerosis?
  Developmental Neuroscience, 1991
• Low arylsulphatase A activity and choreoathetotic syndrome in three siblings: differentiation of pseudodeficiency from metachromatic leukodystrophy
  European Journal of Pediatrics, 1991
• Arylsulfatase A pseudodeficiency: loss of a polyadenylylation signal and N-glycosylation site.
  Proceedings of the National Academy of Sciences, 1989
• Pseudodeficiency of arylsulfatase A: a common genetic polymorphism with possible disease implications
  Human Genetics, 1989
• [66] Activator proteins for lysosomal glycolipid hydrolysis
  Published by Elsevier ,1987
• The activator of cerebroside-sulphatase
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1978
• A COMPARATIVE STUDY OF BRAIN AND KIDNEY GLYCOLIPIDS IN METACHROMATIC LEUCODYSTROPHY*
  Journal of Neurochemistry, 1966
• Sulfatides of human kidney isolation, identification, and fatty acid composition
  Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism, 1966