galactose has been researched along with Mucopolysaccharidosis I 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 |
|---|---|
| Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Cifonelli, JA; Dorfman, A; Knecht, J | 1 |
| Germinario, RJ; Kahlenberg, A; Pinsky, L | 2 |
| Dekaban, AS; Patton, VM | 1 |
| Dorfman, A; Matalon, R | 1 |
| Bach, G; Friedman, R; Neufeld, EF; Weissmann, B | 1 |
| Wherrett, JR | 1 |
8 other study(ies) available for galactose and Mucopolysaccharidosis I
| Article | Year |
|---|---|
Brain sphingolipids in I cell disease (mucolipidosis II).
Topics: Abnormalities, Multiple; Ceramides; Cerebrosides; Child, Preschool; Chromatography, Gas; Chromatography, Thin Layer; Cytoplasmic Granules; Fibroblasts; Galactose; Gangliosides; Glucose; Humans; Lactose; Lipidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Neuraminic Acids; Retinitis Pigmentosa; Sphingolipids; Sphingomyelins; Sulfoglycosphingolipids; Syndrome | 1974 |
Structural studies on heparitin sulfate of normal and Hurler tissues.
Topics: Adolescent; Adult; Amino Acids; Aorta; Autopsy; Child; Child, Preschool; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Galactose; Glycosaminoglycans; Humans; Infant; Liver; Male; Molecular Weight; Mucopolysaccharidosis I; Xylose | 1967 |
The disorder of hyaluronic acid metabolism in cultured skin fibroblasts derived from a patient with the Hurler syndrome.
Topics: Biological Transport; Cells, Cultured; Fibroblasts; Glucose; Glycoside Hydrolases; Hexoses; Humans; Hyaluronic Acid; Isotope Labeling; Kinetics; Mucopolysaccharidosis I; Skin; Time Factors; Tritium; Uronic Acids | 1973 |
Hurler's and Sanfilippo's variants of mucopolysaccharidosis. Cerebral pathology and lipid chemistry.
Topics: Amides; Brain; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Child; Chromatography, Thin Layer; Female; Gangliosides; Glycosaminoglycans; Hexoses; Histocytochemistry; Humans; Intellectual Disability; Lipids; Male; Mucopolysaccharidosis I; Nerve Degeneration | 1971 |
Hurler's syndrome, an -L-iduronidase deficiency.
Topics: Amnion; Carbohydrate Metabolism, Inborn Errors; Diagnosis, Differential; Female; Fibroblasts; Galactosidases; Genes; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Hexoses; Humans; Intellectual Disability; Liver; Lysosomes; Mucopolysaccharidosis I; Phenols; Retinitis Pigmentosa; Skin; Uronic Acids | 1972 |
The defect in the Hurler and Scheie syndromes: deficiency of -L-iduronidase.
Topics: Carbohydrate Metabolism, Inborn Errors; Cell Fractionation; Chromatography, Gas; Corneal Opacity; Fibroblasts; Glycosaminoglycans; Glycoside Hydrolases; Hexoses; Humans; Lysosomes; Methods; Mucopolysaccharidosis I; Retinitis Pigmentosa; Syndrome; Uronic Acids | 1972 |
Biochemical studies on the sulphated glycosaminoglycan fraction of skin fibroblasts cultured from a patient with the Hurler syndrome.
Topics: Cells, Cultured; Chromatography, Ion Exchange; Fibroblasts; Glucose; Glycosaminoglycans; Glycoside Hydrolases; Hexoses; Humans; Isotope Labeling; Mucopolysaccharidosis I; Skin; Sulfates; Sulfur Isotopes; Time Factors; Tritium; Ultrafiltration; Uronic Acids | 1973 |
Analysis of glycolipids in the Hurler syndrome.
Topics: Adolescent; Brain Chemistry; Child; Glycolipids; Hexoses; Humans; Kidney; Liver; Male; Mucopolysaccharidosis I; Spleen | 1968 |