Compounds > galactosamine
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galactosamine and Sphingolipid Storage Diseases

galactosamine has been researched along with Sphingolipid Storage Diseases in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19903 (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
Calatroni, A; Tira, ME1
Sandhoff, K; Zerfowski, J1
O'Brien, JS1

Other Studies

3 other study(ies) available for galactosamine and Sphingolipid Storage Diseases

ArticleYear
Isolation of acidic glycopeptides from urine by means of anion-exchange resins. Application to some cases of glycosphingolipidosis or mucolipidosis.
    Clinica chimica acta; international journal of clinical chemistry, 1976, Sep-06, Volume: 71, Issue:2

    Topics: Amino Acids; Chromatography, Ion Exchange; Galactosamine; Glucosamine; Glycopeptides; Hexoses; Humans; Male; Sialic Acids; Sphingolipidoses

1976
[Juvenile GM2 gangliosidosis with altered substrate specificity of hexosaminidase A (author's transl)].
    Acta neuropathologica, 1974, Mar-26, Volume: 27, Issue:3

    Topics: Adolescent; Ceramides; Female; Galactosamine; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Liver; Neuraminic Acids; Sphingolipidoses

1974
Editorial: Synthetic defect in ganglioside metabolism.
    The New England journal of medicine, 1974, 10-31, Volume: 291, Issue:18

    Topics: Autopsy; Brain; Galactosamine; Gangliosides; Glycolipids; Hexosyltransferases; Humans; Infant; Liver; Male; Sphingolipidoses; Uridine Diphosphate Sugars

1974