Compounds > galactosamine

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galactosamine and Retinitis Pigmentosa

galactosamine has been researched along with Retinitis Pigmentosa in 8 studies

Research

Studies (8)

Timeframe	Studies, this research(%)	All Research%
pre-1990	8 (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
Arbogast, B; Dorfman, A; Matalon, R	1
Constantopoulos, G; Dekabian, AS; Scheie, HG	1
Lee, TY; Onisawa, J	1
Gordon, BA; Haust, MD	2
Constantopoulos, G; Dekaban, AS; Louie, M	1
Dorfman, A; Matalon, R; Stoolmiller, AC; Thompson, JN	1
Minami, R; Nakao, T; Orii, T; Takase, A	1

Other Studies

8 other study(ies) available for galactosamine and Retinitis Pigmentosa

Article	Year
Deficiency of chondroitin sulfate N-acetylgalactosamine 4-sulfate sulfatase in Maroteaux-Lamy syndrome. Biochemical and biophysical research communications, 1974, Dec-23, Volume: 61, Issue:4 Topics: Cells, Cultured; Chondroitin; Fibroblasts; Galactosamine; Humans; Intellectual Disability; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Skin; Sulfatases; Sulfuric Acids; Syndrome	1974
Heterogeneity of disorders in patients with corneal clouding, normal intellect, and mucopolysaccharidosis. American journal of ophthalmology, 1971, Volume: 72, Issue:6 Topics: Adolescent; Adult; Carbohydrate Metabolism, Inborn Errors; Child; Chondroitin; Corneal Opacity; Female; Galactosamine; Glycosaminoglycans; Hexosamines; Humans; Intelligence; Male; Methods; Mucopolysaccharidoses; Radiography; Retinitis Pigmentosa; Sulfates; Visual Acuity	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
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
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
N-acetyl-beta-hexosaminidase: role in the degradation of glycosaminoglycans. Science (New York, N.Y.), 1973, Aug-31, Volume: 181, Issue:4102 Topics: Carbohydrate Metabolism, Inborn Errors; Carbon Isotopes; Cells, Cultured; Coumarins; Fibroblasts; Galactosamine; Glycosaminoglycans; Hexosaminidases; Humans; Intellectual Disability; Lipidoses; Mucopolysaccharidoses; Oligosaccharides; Retinitis Pigmentosa	1973
Pattern of urinary acid mucopolysaccharide excretion in five patients with genetic mucopolysaccharidoses. The Tohoku journal of experimental medicine, 1973, Volume: 110, Issue:1 Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chondroitin; Chromatography; Corneal Opacity; Electrophoresis; Female; Galactosamine; Glycosaminoglycans; Heparitin Sulfate; Hexosamines; Humans; Hyaluronic Acid; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Retinitis Pigmentosa; Sulfates; Uronic Acids	1973