Page last updated: 2024-08-22

galactosamine and Gargoylism, Hunter Syndrome

galactosamine has been researched along with Gargoylism, Hunter Syndrome in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19905 (100.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Gibbs, DA; Purkiss, P; Watts, RW1
Miyawaki, T; Moriya, N; Okuda, N; Taniguchi, N1
Cunningham, WL; Ramage, P1
Gordon, BA; Haust, MD2

Other Studies

5 other study(ies) available for galactosamine and Gargoylism, Hunter Syndrome

ArticleYear
Studies on the composition of urinary glycosaminoglycans and oligosaccharides in patients with mucopolysaccharidoses who were receiving fibroblast transplants.
    Clinica chimica acta; international journal of clinical chemistry, 1983, Jun-30, Volume: 131, Issue:1-2

    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.
    Clinica chimica acta; international journal of clinical chemistry, 1975, May-01, Volume: 60, Issue:3

    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.
    Biochimica et biophysica acta, 1975, Dec-05, Volume: 411, Issue:2

    Topics: Child; Dermatan Sulfate; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Humans; Male; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Sulfuric Acids; Uronic Acids

1975
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