glucosamine has been researched along with Intellectual Disability in 26 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 25 (96.15) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (3.85) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Coppa, GV; Gabrielli, O; Galeazzi, T; Galeotti, F; Maccari, F; Mantovani, V; Marchesiello, RL; Padella, L; Santoro, L; Volpi, N; Zampini, L | 1 |
| Autio, S; Härö, E; Kivimäki, T; Koskela, SL; Näntö, V; Näntö-Salonen, K; Penttinen, R | 1 |
| Becker, C; Gehler, J; Hartmann, J; Sewell, AC; Spranger, J | 2 |
| Borud, O; Lie, SO; Strömme, JH; Torp, KH | 1 |
| Borud, O; Torp, KH | 1 |
| Borud, O; Dahl, T; Torp, KH | 1 |
| Jaeken, J | 1 |
| Lamberg, SI; Stoolmiller, AC | 1 |
| Jenner, FA; Merskey, H; Pollitt, RJ | 1 |
| Eriksson, O; Hultberg, B; Ockerman, PA | 1 |
| Bach, G; Berman, ER; Vered, J | 1 |
| Carrel, RE; Fluharty, AL; Kihara, H; Lassila, EL; Porter, MT; Trammell, J | 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 |
| London, KJ; Murphy, D; Pennock, CA | 1 |
| Autio, S; Järvinen, H; Visakorpi, JK | 1 |
| Aula, P; Autio, S; Näntö, V; Raivio, K | 1 |
| Autio, S | 1 |
| Arstila, AU; Autio, S; Palo, J; Riekkinen, P | 1 |
| Autio, S; Palo, J | 2 |
| Chow, A; Hudgin, RL; Michaels, MA; Mookerjea, S; Moscarello, MA; Schachter, H | 1 |
2 review(s) available for glucosamine and Intellectual Disability
| 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 |
24 other study(ies) available for glucosamine and Intellectual Disability
| Article | Year |
|---|---|
Mental retardation in mucopolysaccharidoses correlates with high molecular weight urinary heparan sulphate derived glucosamine.
Topics: Adolescent; Adult; Child; Child, Preschool; Female; Glucosamine; Heparitin Sulfate; Humans; Infant; Intellectual Disability; Male; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis III; Reference Values; Young Adult | 2015 |
Metabolism of collagen in aspartylglycosaminuria: urinary excretion of hydroxyproline.
Topics: Acetylglucosamine; Adolescent; Adult; Age Factors; Child; Child, Preschool; Collagen; Connective Tissue Diseases; Female; Glucosamine; Humans; Hydroxyproline; Infant; Intellectual Disability; Male; Metabolism, Inborn Errors; Middle Aged; Reference Values | 1984 |
Clinical and biochemical delineation of aspartyl-glycosaminuria as observed in two members of an Italian family.
Topics: Abnormalities, Multiple; Acetylglucosamine; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Fabry Disease; Facial Bones; Female; Glucosamine; Humans; Intellectual Disability; Italy; Male; Pedigree; Skull | 1981 |
Aspartylglycosaminuria in an Italian family: clinical and biochemical characteristics.
Topics: Acetylglucosamine; Adult; Amidohydrolases; Aspartylglucosaminuria; Child; Consanguinity; Female; Glucosamine; Humans; Intellectual Disability; Leukocytes; Male; Oligosaccharides; Pedigree | 1981 |
Aspartylglycosaminuria in Northern Norway in eight patients: clinical heterogeneity and variations with the diet.
Topics: Acetylglucosamine; Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Creatinine; Dietary Proteins; Female; Glucosamine; Humans; Intellectual Disability; Male; Mucolipidoses | 1978 |
[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 |
Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation.
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Aspartylglucosaminuria; Child; Child, Preschool; Glucosamine; Humans; Intellectual Disability; Mucolipidoses | 1978 |
[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 |
Aspartylglycosaminuria. An inborn error of metabolism associated with mental defect.
Topics: Adult; Asparagine; Aspartic Acid; Female; Glucosamine; Glucosidases; Glycoproteins; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors; Oligosaccharides; Peptide Hydrolases | 1968 |
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 |
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 |
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 |
Gas-liquid chromatographic measurement of glucosamine and galactosamine content of urinary glycosaminoglycans.
Topics: Acetamides; Borohydrides; Cartilage; Chondroitin; Chromatography, Gas; Evaluation Studies as Topic; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Hyaluronic Acid; Intellectual Disability; Methods; Mucopolysaccharidoses; Sulfuric Acids; Syndrome; Time Factors | 1974 |
Aspartylglycosaminuria (AGU). Further aspects on its clinical picture, mode of inheritance and epidemiology based on a series of 57 patients.
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Bone Marrow; Child; Child, Preschool; Consanguinity; Face; Female; Finland; Genes, Recessive; Glucosamine; Homozygote; Humans; Inclusion Bodies; Infant; Infant, Newborn; Intellectual Disability; Lymphocytes; Male; Metabolism, Inborn Errors; Osteochondritis; Radiography; Syndrome | 1973 |
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 |
Biochemical and fine structural studies in aspartylglucosaminuria.
Topics: Age Factors; Amino Acid Metabolism, Inborn Errors; Aspartate Aminotransferases; Bone Diseases; Brain; Glucosamine; Hexosaminidases; Humans; Infections; Intellectual Disability; Liver | 1972 |
Picture of the Month. Aspartylglucosaminuria.
Topics: Adolescent; Aspartic Acid; Body Height; Child; Child, Preschool; Chromatography, Thin Layer; Chromosome Aberrations; Chromosome Disorders; Electrophoresis; Face; Female; Finland; Genes, Recessive; Glucosamine; Humans; Intellectual Disability; Male; Metabolism, Inborn Errors | 1974 |
[Aspartylglucosaminuria].
Topics: Adolescent; Adult; Amidohydrolases; Aspartic Acid; Child; Child, Preschool; Female; Glucosamine; Humans; Infant; Intellectual Disability; Lysosomes; Male; Metabolism, Inborn Errors | 1972 |
The levels of nucleotide-sugar: glycoprotein sialyl- and N-acetylglucosaminyltransferases in normal and pathological human sera.
Topics: Adolescent; Adult; Asthma; Carbon Isotopes; Child; Child, Preschool; Cystic Fibrosis; Cytosine Nucleotides; Glucosamine; Glucosyltransferases; Humans; Infections; Intellectual Disability; Leukemia; Liver Diseases; Neuraminic Acids; Nucleoside Diphosphate Sugars; Transferases; Uracil Nucleotides | 1972 |