glucosamine has been researched along with Carbohydrate Metabolism, Inborn Error in 30 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 30 (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; Hancock, LW; Horwitz, AL | 1 |
| Maury, CP | 1 |
| Dickersin, R; Dvorak, AM; Friedman, RB; Kistler, JP; Kolodny, EH; Lott, IT; Mihm, MC; Nersasian, R; Schnur, J | 1 |
| Borud, O; Torp, KH | 1 |
| Collart, M; Humbel, R | 1 |
| Dawson, G; Tsay, GC | 1 |
| Autio, S; Haltia, M; Palo, J | 1 |
| Jaeken, J | 1 |
| Lamberg, SI; Stoolmiller, AC | 1 |
| Ockerman, PA | 2 |
| Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
| Bach, G; Berman, ER; Vered, J | 1 |
| Lee, TY; Onisawa, J | 1 |
| Carrel, RE; Fluharty, AL; Kihara, H; Lassila, EL; Porter, MT; Trammell, J | 1 |
| Callahan, JW; Pinsky, L; Wolfe, LS | 1 |
| Palo, J; Savolainen, H | 1 |
| Gordon, BA; Haust, MD | 2 |
| Harvey, J; Robertson, WV | 1 |
| Benson, PF; Dean, MF; Muir, H | 1 |
| Bach, G; Cantz, M; Eisenberg, F; Neufeld, EF | 1 |
| Humbel, R | 1 |
| Callahan, JW; Wolfe, LS | 1 |
| Ng-Ying-Kin, NM; Senior, RG; Wolfe, LS | 1 |
| Aula, P; Autio, S; Näntö, V; Raivio, K | 1 |
| Autio, S | 1 |
| Jolly, RD; Lundblad, A; Nordén, NE; Ockerman, PA | 1 |
| Brun, A; Gamstorp, I; Kjellman, B; Ockerman, PA; Palmgren, B | 1 |
| Montreuil, J; Strecker, G | 1 |
2 review(s) available for glucosamine and Carbohydrate Metabolism, Inborn Error
| 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 |
Aspartylglycosaminuria. Analysis of thirty-four patients.
Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Aspartic Acid; Birth Order; Birth Weight; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Electrocardiography; Electroencephalography; Female; Finland; Geography; Glucosamine; Humans; Infant; Intellectual Disability; Intelligence Tests; Life Expectancy; Male; Pedigree; Socioeconomic Factors | 1972 |
28 other study(ies) available for glucosamine and Carbohydrate Metabolism, Inborn Error
| Article | Year |
|---|---|
N-acetylneuraminic acid and sialoglycoconjugate metabolism in fibroblasts from a patient with generalized N-acetylneuraminic acid storage disease.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Gangliosides; Glucosamine; Hexosamines; Humans; N-Acetylneuraminic Acid; Reference Values; Sialic Acids; Sialoglycoproteins; Skin; Tritium | 1983 |
Detection of aspartylglycosaminuria by gas--liquid chromatography.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Amino Acid Metabolism, Inborn Errors; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Glucosamine; Humans; Middle Aged | 1981 |
Mannosidosis. New clinical presentation, enzyme studied, and carbohydrate analysis.
Topics: Adult; Carbohydrate Metabolism, Inborn Errors; Child; Disaccharidases; Galactose; Gingiva; Gingival Hyperplasia; Glucosamine; Humans; Hydrogen-Ion Concentration; Male; Mannose; Mannosidases | 1977 |
[Aspartylglucosaminuria. A hereditary disease with unusual high incidence among Finns in northern Norway].
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Asparagine; Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Finland; Glucosamine; Humans; Infant; Intellectual Disability; Male; Norway | 1978 |
Oligosaccharides in urine of patients with glycoprotein storage diseases. I. Rapid detection by thin-layer chromatography.
Topics: Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glucosamine; Glycoproteins; Humans; Mannose; Methods; Oligosaccharides; Time Factors | 1975 |
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 |
Aspartylglycosaminuria: a generalized storage disease. Morphological and histochemical studies.
Topics: Adult; Amidohydrolases; Aspartylglucosylaminase; Autopsy; Biopsy; Brain; Carbohydrate Metabolism, Inborn Errors; Female; Glucosamine; Humans; Kupffer Cells; Liver; Lysosomes; Macrophages; Microscopy, Electron; Neurons | 1975 |
[A not-previously described hereditary neurological disease with a deficiency of sialic acid, galactose and N-acetylglucosamine of plasma glycoproteins].
Topics: Acetylglucosamine; Carbohydrate Metabolism, Inborn Errors; Child, Preschool; Demyelinating Diseases; Diseases in Twins; Female; Galactose; Glucosamine; Humans; Intellectual Disability; Sialic Acids; Syndrome; Twins, Monozygotic | 1989 |
Diseases of glycoprotein storage.
Topics: Brain; Carbohydrate Metabolism, Inborn Errors; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Lipidoses; Liver; Mannose; Mucopolysaccharidoses | 1969 |
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
Topics: Acid Phosphatase; Brain; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gel; Fucose; Galactosidases; Glucosamine; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Hot Temperature; Humans; Intellectual Disability; Kidney; Mannose; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Spleen | 1969 |
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 |
Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
Topics: Amino Acids; Aspartic Acid; Bone and Bones; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glutamates; Glycine; Glycosaminoglycans; Humans; Hypertrichosis; Joint Diseases; Male; Mucopolysaccharidosis I; Retinitis Pigmentosa; Serine; Uronic Acids | 1970 |
Acid glycosidases in mucopolysaccharidoses fibroblasts.
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Electrophoresis; Female; Fibroblasts; Fluorometry; Galactosidases; Glucosamine; Glucosephosphate Dehydrogenase; Glucuronidase; Glycosaminoglycans; Glycoside Hydrolases; Humans; Intellectual Disability; Male; Mucopolysaccharidoses; Retinitis Pigmentosa; Spectrophotometry | 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 |
Studies on serum and urinary glycopeptides and glycosaminoglycans in aspartylglucosaminuria.
Topics: Amidohydrolases; Aspartic Acid; Carbohydrate Metabolism, Inborn Errors; Carbohydrates; Chromatography, Thin Layer; Electrophoresis; Glucosamine; Glucuronidase; Glycopeptides; Glycosaminoglycans; Humans; Hyaluronoglucosaminidase; Hydrogen-Ion Concentration; Lysosomes; Neuraminic Acids; Peptides | 1972 |
The mucopolysaccharidoses types I, II, and 3: urinary findings in 23 cases.
Topics: Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Gas; Chromatography, Gel; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Hexosamines; Humans; Hyaluronoglucosaminidase; Infant; Intellectual Disability; Male; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Retinitis Pigmentosa; Sulfates; Testis; Uronic Acids | 1970 |
Hepatic acid mucopolysaccharides in the mucopolysaccharidoses type I, II and 3.
Topics: Carbohydrate Metabolism, Inborn Errors; Chromatography, Gel; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Hexosamines; Humans; Intellectual Disability; Liver; Molecular Weight; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Placenta; Pregnancy; Retinitis Pigmentosa; Sulfates; Umbilical Cord; Uronic 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 |
Mobilization of glycosaminoglycans by plasma infusion in mucopolysaccharidosis type 3--two types of response.
Topics: Adolescent; Blood Transfusion; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Child; Chromatography, Gel; Chromatography, Ion Exchange; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Heparitin Sulfate; Humans; Intellectual Disability; Male; Molecular Weight; Plasma; Time Factors; Uronic Acids | 1973 |
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 |
Isolation and characterization of keratan sulfates from the liver of a patient with GM1-gangliosidosis type I.
Topics: Animals; Autopsy; Carbohydrate Metabolism, Inborn Errors; Cattle; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Chromatography, Thin Layer; Galactose; Galactosidases; Gangliosides; Glucosamine; Glycosaminoglycans; Glycoside Hydrolases; Humans; Keratins; Liver; Lysosomes; Periodic Acid; Pyridinium Compounds; Solubility; Sulfuric Acids | 1970 |
The structures of oligosaccharides accumulating in the liver of G-M1-gangliosidosis, type I.
Topics: Acetamides; Carbohydrate Metabolism, Inborn Errors; Chromatography, Gas; Galactose; Gangliosides; Glucosamine; Glycoside Hydrolases; Hexosamines; Hexoses; Humans; Isotope Labeling; Liver; Magnetic Resonance Spectroscopy; Mannose; Mass Spectrometry; Methylation; Molecular Weight; Oligosaccharides; Periodic Acid; Spectrophotometry, Infrared; Stereoisomerism; Tritium | 1974 |
Detection of heterozygotes for aspartylglucosaminuria (AGU) in cultured fibroblasts.
Topics: Amidohydrolases; Amniocentesis; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Family; Female; Fibroblasts; Glucosamine; Heterozygote; Hexosaminidases; Humans; Intellectual Disability; Lysosomes; Pregnancy; Prenatal Diagnosis | 1974 |
Mannosidosis in Angus cattle: partial characterization of two mannose containing oligosaccharides.
Topics: Animals; Brain; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Cattle; Cattle Diseases; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Glucosamine; Heterozygote; Humans; Mannose; Oligosaccharides; Optical Rotation; Ultrafiltration | 1973 |
Mannosidosis: isolation of oligosaccharide storage material from brain.
Topics: Amino Acids; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Chromatography; Chromatography, Gel; Diagnosis, Differential; Fucose; Galactose; Glucosamine; Glucose; Glycoside Hydrolases; Hexosamines; Humans; Liver; Mannose; Monosaccharides; Mucopolysaccharidoses; Neuraminic Acids; Oligosaccharides; Uronic Acids | 1969 |
Mannosidosis: a clinical and histopathologic study.
Topics: Bone Marrow Cells; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diagnosis, Differential; Glucosamine; Glycoside Hydrolases; Humans; Infant; Liver; Lymph Nodes; Male; Mannose; Mucopolysaccharidoses; Radiography | 1969 |
[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 |