Page last updated: 2024-08-22

glucosamine and Retinitis Pigmentosa

glucosamine has been researched along with Retinitis Pigmentosa in 12 studies

Research

Studies (12)

Timeframe	Studies, this research(%)	All Research%
pre-1990	12 (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

Authors	Studies
Lamberg, SI; Stoolmiller, AC	1
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
Gordon, BA; Haust, MD	2
Harvey, J; Robertson, WV	1
Constantopoulos, G; Dekaban, AS; Louie, M	1
Bach, G; Cantz, M; Eisenberg, F; Neufeld, EF	1
Humbel, R	1
Bach, G; Cantz, M; Chrambach, A; Neufeld, EF	1

Reviews

1 review(s) available for glucosamine and Retinitis Pigmentosa

Article	Year
Glycosaminoglycans. A biochemical and clinical review. The Journal of investigative dermatology, 1974, Volume: 63, Issue:6 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

Article

Year

Glycosaminoglycans. A biochemical and clinical review.

The Journal of investigative dermatology, 1974, Volume: 63, Issue:6

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

Other Studies

11 other study(ies) available for glucosamine and Retinitis Pigmentosa

Article	Year
Enzyme patterns in tissues and body fluids in mucopolysaccharidoses. Clinica chimica acta; international journal of clinical chemistry, 1969, Volume: 25, Issue:1 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. Clinical chemistry, 1971, Volume: 17, Issue:9 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. Biochemical medicine, 1970, Volume: 3, Issue:5 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. Biochemical medicine, 1970, Volume: 4, Issue:2 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. Clinical biochemistry, 1970, Volume: 3, Issue:3 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. Clinical biochemistry, 1971, Volume: 4, Issue: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. Biochemical medicine, 1972, Volume: 6, Issue:3 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
Acid mucopolysaccharides (glycosaminoglycans) in normal human kidneys and in kidneys of patients with mucopolysaccharidoses. Biochemical medicine, 1973, Volume: 7, Issue:3 Topics: Adolescent; Adult; Cetylpyridinium; Chemical Precipitation; Child; Chondroitin; Chromatography, Ion Exchange; Ethanol; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Hyaluronic Acid; Kidney; Kidney Cortex; Kidney Medulla; Lyases; Male; Middle Aged; Mucopolysaccharidoses; Peptide Hydrolases; Retinitis Pigmentosa; Uronic Acids	1973
The defect in the Hunter syndrome: deficiency of sulfoiduronate sulfatase. Proceedings of the National Academy of Sciences of the United States of America, 1973, Volume: 70, Issue:7 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. Clinica chimica acta; international journal of clinical chemistry, 1974, Volume: 52, Issue:2 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
The Hunter corrective factor. Purification and preliminary characterization. The Journal of biological chemistry, 1972, Sep-10, Volume: 247, Issue:17 Topics: Ammonium Sulfate; Cells, Cultured; Chemical Precipitation; Chondroitin; Chromatography, Affinity; Chromatography, Gel; Electrophoresis; Fibroblasts; Glucosamine; Humans; Isoelectric Focusing; Macromolecular Substances; Molecular Weight; Mucopolysaccharidosis II; Proteins; Proteinuria; Retinitis Pigmentosa; Skin; Sulfates; Sulfur Isotopes; Tritium	1972