galactosamine has been researched along with Mucopolysaccharidosis I in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 7 (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 |
---|---|
Gibbs, DA; Purkiss, P; Watts, RW | 1 |
Miyawaki, T; Moriya, N; Okuda, N; Taniguchi, N | 1 |
Cunningham, WL; Ramage, P | 1 |
Berman, ER; Kohn, G; Stein, H; Yatziv, S | 1 |
Lee, TY; Onisawa, J | 1 |
Gordon, BA; Haust, MD | 2 |
7 other study(ies) available for galactosamine and Mucopolysaccharidosis I
Article | Year |
---|---|
Studies on the composition of urinary glycosaminoglycans and oligosaccharides in patients with mucopolysaccharidoses who were receiving fibroblast transplants.
Topics: Child; Female; Fibroblasts; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Male; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Oligosaccharides; Uronic Acids | 1983 |
Molecular size difference of urinary heparan sulfates from normal individuals and genetic mucopolysaccharidoses.
Topics: Adolescent; Child; Child, Preschool; Chromatography, Gel; Chromatography, Thin Layer; Electrophoresis, Cellulose Acetate; Galactosamine; Glucosamine; Glycosaminoglycans; Heparitin Sulfate; Humans; Male; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III | 1975 |
Comparative structural studies of urinary glycosaminoglycans in the Hurler and Hunter syndromes.
Topics: Child; Dermatan Sulfate; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Male; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Sulfuric Acids; Uronic Acids | 1975 |
Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis. 3 (pseudo-Hurler polydystrophy).
Topics: Chromatography, Ion Exchange; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Fucose; Galactosamine; Glucuronidase; Glycoproteins; Glycoside Hydrolases; Humans; Hydrolases; Leukocytes; Lipid Metabolism, Inborn Errors; Mucopolysaccharidosis I; Neuraminic Acids; Proteinuria; Skin; Sulfuric Acids; Uronic Acids | 1974 |
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 |
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 |