galactose has been researched along with ARSA Deficiency in 8 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 8 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Aoki, K; Handa, S; Yamaguchi, S; Yamakawa, T | 1 |
Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
Brady, RO | 1 |
Eto, Y; Herschkowitz, NN; Rampini, S; Wiesmann, U | 1 |
Dulaney, JT; Moser, HW; Sugita, M | 1 |
Hiatt, W; Sattler, M; Wenger, DA | 1 |
Eto, Y; Herschkowitz, NN; Wiesmann, U | 1 |
Mechler, L; Meurant, C; Philippart, M; Sarlieve, L | 1 |
2 review(s) available for galactose and ARSA Deficiency
Article | Year |
---|---|
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses | 1976 |
Disorders of lipid metabolism.
Topics: Adult; Animals; Bone Marrow; Cell Line; Ceramides; Child; Fabry Disease; Fucose; Galactose; Gangliosides; Gaucher Disease; Genetic Variation; Glycolipids; Glycoside Hydrolases; Humans; Leukemia, Myeloid; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipidoses; Mice; Niemann-Pick Diseases; Sulfoglycosphingolipids | 1972 |
6 other study(ies) available for galactose and ARSA Deficiency
Article | Year |
---|---|
Deficiency of seminolipid sulphatase activity in brain tissue of metachromatic leucodystrophy.
Topics: Acid Phosphatase; Animals; Arylsulfatases; Brain; Cerebrosides; Galactose; Glycolipids; Humans; Hydrogen-Ion Concentration; Leukodystrophy, Metachromatic; Male; Manganese; Mice; Sulfatases; Sulfoglycosphingolipids; Sulfuric Acids; Taurocholic Acid | 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 sulphatases.
Topics: Adult; Brain; Cerebrosides; Child; Child, Preschool; Cholesterol; Chromatography, Thin Layer; Coumarins; Dehydroepiandrosterone; Estrone; Galactose; Galactosidases; Genetic Variation; Glycosides; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoelectric Focusing; Kidney; Kinetics; Leukodystrophy, Metachromatic; Liver; Lysophosphatidylcholines; Lysosomes; Organ Specificity; Polyethylene Glycols; Solubility; Sphingosine; Sulfatases; Tritium | 1974 |
Structure and composition of sulfatides isolated from livers of patients with metachromatic leukodystrophy: galactosyl sulfatide and lactosyl sulfatide.
Topics: Adolescent; Child, Preschool; Chromatography; Chromatography, Gas; Chromatography, Ion Exchange; Chromatography, Thin Layer; Drug Stability; Fatty Acids; Freezing; Galactose; Humans; Lactose; Leukodystrophy, Metachromatic; Liver; Male; Silicon Dioxide; Spectrophotometry, Infrared; Sulfoglycosphingolipids; Time Factors | 1974 |
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.
Topics: Adult; Brain; Ceramides; Female; Galactose; Galactosidases; Gangliosides; Humans; Infant; Lactose; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Liver; Male; Niemann-Pick Diseases; Skin; Spleen; Syndrome | 1974 |
Sulfogalactosylsphingosine sulfatase. Characteristics of the enzyme and its deficiency in metachromatic leukodystrophy in human cultured skin fibroblasts.
Topics: Barium; Cells, Cultured; Cholic Acids; Chromatography, Thin Layer; Copper; Deoxycholic Acid; Drug Stability; Fibroblasts; Galactose; Humans; Hydrogen-Ion Concentration; Isoelectric Focusing; Kinetics; Leukodystrophy, Metachromatic; Manganese; Mercury; Skin; Sphingosine; Sulfatases; Sulfur Radioisotopes; Surface-Active Agents; Taurocholic Acid; Temperature; Time Factors; Zinc | 1974 |
Human urinary sulfatides in patients with sulfatidosis (metachromatic leukodystrophy).
Topics: Adolescent; Adult; Aged; Cerebrosides; Child; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Heterozygote; Hexoses; Humans; Infant; Kidney; Leukodystrophy, Metachromatic; Male; Middle Aged; Sulfatases; Sulfoglycosphingolipids | 1971 |