galactose has been researched along with Pigmentary Retinopathy in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (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 |
|---|---|
| Lamberg, SI; Stoolmiller, AC | 1 |
| Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Bach, G; Berman, ER; Vered, J | 1 |
| Taniguchi, N | 1 |
| Harvey, J; Robertson, WV | 1 |
| Bach, G; Cantz, M; Eisenberg, F; Neufeld, EF | 1 |
| Humbel, R | 1 |
| Hall, CW; Neufeld, EF | 1 |
| Dorfman, A; Matalon, R | 1 |
| Bach, G; Friedman, R; Neufeld, EF; Weissmann, B | 1 |
1 review(s) available for galactose and Pigmentary Retinopathy
| Article | Year |
|---|---|
Glycosaminoglycans. A biochemical and clinical review.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chondroitin; Cornea; Corneal Opacity; Dermatan Sulfate; Fibroblasts; Galactose; Glucosamine; Glycosaminoglycans; Heparin; Humans; Hyaluronic Acid; Hyaluronoglucosaminidase; Intellectual Disability; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Proteoglycans; Retinitis Pigmentosa; Skin; Staining and Labeling; Sulfatases; Testis | 1974 |
9 other study(ies) available for galactose and Pigmentary Retinopathy
| 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 |
A reliable spot test for mucopolysaccharidoses.
Topics: Adult; Bone Diseases, Developmental; Carbazoles; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Coloring Agents; Corneal Opacity; Dialysis; Dwarfism; Female; Galactose; Glucosamine; Glycosaminoglycans; Hexosamines; Humans; Indicators and Reagents; Infant; Intellectual Disability; Male; Methods; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Onium Compounds; Paper; Peptide Hydrolases; Phenols; Retinitis Pigmentosa; Sulfuric Acids; Toluene; Uronic Acids | 1971 |
Age differences in the pattern of urinary glycosaminoglycan excretion in normal individuals.
Topics: Adolescent; Adult; Age Factors; Aged; Child; Child, Preschool; Chondroitin; Chromatography, Gas; Chromatography, Ion Exchange; Diagnosis, Differential; Electrophoresis; Female; Galactose; Glycosaminoglycans; Heparitin Sulfate; Hexosamines; Humans; Hyaluronoglucosaminidase; Lyases; Male; Methods; Middle Aged; Mucopolysaccharidoses; Retinitis Pigmentosa; Serine; Sulfuric Acids; Testis; Xylose | 1972 |
The determination of galactose in urinary acidic glycosaminoglycans as a measure of keratan sulfate-like substances in urine.
Topics: Achondroplasia; Adolescent; Adult; Aged; Aging; Arthritis, Rheumatoid; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Ion Exchange; Chromatography, Thin Layer; Colorimetry; Dermatomyositis; Female; Galactose; Glucosamine; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Infant; Infant, Newborn; Intellectual Disability; Lipid Metabolism, Inborn Errors; Male; Methods; Middle Aged; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfuric Acids | 1972 |
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Galactose; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycosides; Humans; Iduronic Acid; Intellectual Disability; Mannose; Mucopolysaccharidosis II; Retinitis Pigmentosa; Skin; Sulfatases; Sulfur Isotopes; Sulfuric Acids; Tritium; Uronic Acids | 1973 |
Identification and quantitation of keratan sulfate in urine.
Topics: Adult; Athetosis; Carbohydrate Metabolism, Inborn Errors; Child; Chromatography, Ion Exchange; Chromatography, Thin Layer; Evaluation Studies as Topic; Fucose; Galactose; Glucosamine; Glycosaminoglycans; Humans; Methods; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa | 1974 |
Alpha-L-iduronidase activity in cultured skin fibroblasts and amniotic fluid cells.
Topics: Adult; Amniotic Fluid; Cells, Cultured; Child; Corneal Opacity; Female; Fibroblasts; Galactosidases; Glucuronidase; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Hexoses; Humans; Mucopolysaccharidoses; Pregnancy; Retinitis Pigmentosa; Skin; Syndrome; Uronic Acids | 1973 |
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 |