glucosamine has been researched along with Lipid Metabolism, Inborn Error in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (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 |
|---|---|
| Dawson, G; Tsay, GC | 1 |
| Dacremont, G; Kint, JA | 1 |
| Callahan, JW; Pinsky, L; Wolfe, LS | 1 |
| Bianchi, E; Lanzi, G; Magrini, U; Severi, F; Tettamanti, G | 1 |
| Harvey, J; Robertson, WV | 1 |
| Ng-Ying-Kin, NM; Wolfe, LS | 1 |
| Batt, RD; Hocking, JD; Jolly, RD | 1 |
| Montreuil, J; Strecker, G | 1 |
| Fluharty, AL; Kihara, H; Porter, MT | 1 |
9 other study(ies) available for glucosamine and Lipid Metabolism, Inborn Error
| Article | Year |
|---|---|
Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolism.
Topics: alpha-L-Fucosidase; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Fucose; Galactose; Galactosidases; Glucosamine; Glycopeptides; Hexosaminidases; Humans; Lipid Metabolism, Inborn Errors; Mannose; Mannosidases; Metabolism, Inborn Errors; Sialic Acids; Skin | 1975 |
The biochemical abnormalities in Fabry's disease.
Topics: Adult; Cerebrosides; Child; Colorimetry; Female; Fluorometry; Galactosidases; Glucosamine; Glycolipids; Glycoside Hydrolases; Hexosamines; Humans; Leukocytes; Lipid Metabolism, Inborn Errors; Male | 1970 |
G M1 -gangliosidosis (Type II): studies on a fibroblast cell strain.
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Carbon Isotopes; Child, Preschool; Chromatography; Chromatography, Gel; Chromatography, Thin Layer; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glucosamine; Glycolipids; Glycosaminoglycans; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Skin | 1970 |
Infantile GM1 gangliosidosis. Histochemical, ultrastructural and biochemical studies.
Topics: Biopsy; Brain; Chromatography, Thin Layer; Gangliosides; Glucosamine; Glycosaminoglycans; Histocytochemistry; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lipid Metabolism, Inborn Errors; Liver; Lymphocytes; Male; Microscopy, Electron; Neuraminic Acids | 1971 |
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 |
Oligosaccharides accumulating in the liver from a patient with GM2-gangliosidosis variant O (Sandhoff-Jatzkewitz disease).
Topics: Binding Sites; Child, Preschool; Chromatography, Gas; Chromatography, Gel; Computers; Deuterium; Gangliosides; Glucosamine; Humans; Lipid Metabolism, Inborn Errors; Liver; Magnetic Resonance Spectroscopy; Mannose; Mass Spectrometry; Methylation; Molecular Conformation; Oligosaccharides; Oxidation-Reduction | 1974 |
Deficiency of alpha-mannosidase in Angus cattle. An inherited lysosomal storage disease.
Topics: Animals; Brain; Cattle; Cattle Diseases; Chick Embryo; Chromatography, Paper; Female; Glucosamine; Hexosaminidases; Hexoses; Lipid Metabolism, Inborn Errors; Liver; Lymph Nodes; Lysosomes; Male; Mannose | 1972 |
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency].
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids | 1971 |
Metachromatic leukodystrophy: arylsulfatase-A deficiency in skin fibroblast cultures.
Topics: Biopsy; Cell Line; Child; Culture Techniques; Diffuse Cerebral Sclerosis of Schilder; Fibroblasts; Galactosidases; Glucosamine; Glucuronidase; Glycoside Hydrolases; Humans; Leukocytes; Lipid Metabolism, Inborn Errors; Male; Pedigree; Skin; Sulfatases | 1969 |