Page last updated: 2024-08-17

galactose and Cherry Red Spot Myoclonus Syndrome

galactose has been researched along with Cherry Red Spot Myoclonus Syndrome in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19905 (83.33)18.7374
1990's0 (0.00)18.2507
2000's1 (16.67)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Kotani, M; Sakuraba, H; Yamada, H1
Vladutiu, GD1
Eto, Y; Maekawa, K; Mori, T; Ohta, H1
Berra, B; Borrone, C; Caimi, L; Durand, P; Gatti, R; Martin, JJ; Omodeo Sale, F; Tettamanti, G1
Endo, H; Nagashima, K; Nakamura, N; Shimada, Y; Suzuki, Y; Yotsumoto, H1
Garvin, AJ; Neufeld, EF; Rome, LH; Sando, GN1

Other Studies

6 other study(ies) available for galactose and Cherry Red Spot Myoclonus Syndrome

ArticleYear
Cytochemical and biochemical detection of intracellularly accumulated sialyl glycoconjugates in sialidosis and galactosialidosis fibroblasts with Macckia amurensis.
    Clinica chimica acta; international journal of clinical chemistry, 2004, Volume: 344, Issue:1-2

    Topics: Blotting, Western; Cells, Cultured; Clinical Laboratory Techniques; Fibroblasts; Galactose; Glycoconjugates; Humans; Lysosomal Storage Diseases; Maackia; Mucolipidoses; N-Acetylneuraminic Acid; Plant Lectins; Staining and Labeling

2004
Effect of the co-existence of galactosyl and phosphomannosyl residues on beta-hexosaminidase on the processing and transport of the enzyme in mucolipidosis I fibroblasts.
    Biochimica et biophysica acta, 1983, Nov-08, Volume: 760, Issue:3

    Topics: beta-N-Acetylhexosaminidases; Biological Transport; Cells, Cultured; Chemical Phenomena; Chemistry; Endocytosis; Fibroblasts; Galactose; Hexosaminidases; Hexosephosphates; Humans; Mannosephosphates; Mucolipidoses; Oligosaccharides; Ricin

1983
Neonatal I-cell disease: clinical and biochemical observations.
    Journal of inherited metabolic disease, 1981, Volume: 4, Issue:2

    Topics: Brain; Female; Hexosamines; Hexoses; Humans; Hydrolases; Infant, Newborn; Infant, Newborn, Diseases; Kidney; Liver; Mucolipidoses; Sialic Acids

1981
Mucolipidosis IV, a sialolipidosis due to ganglioside sialidase deficiency.
    Journal of inherited metabolic disease, 1982, Volume: 5, Issue:4

    Topics: Adult; Complement C1; Female; Fibroblasts; Gangliosides; Hexoses; Humans; Leukocytes; Mucolipidoses; Neuraminidase; Proteins; Sialic Acids; Skin

1982
Macular cherry-red spots and beta-galactosidase deficiency in an adult. An autopsy case with progressive cerebellar ataxia, myoclonus, thrombocytopathy, and accumulation of polysaccharide in liver.
    Archives of neurology, 1977, Volume: 34, Issue:3

    Topics: Adult; Blood Platelet Disorders; Brain; Cerebellar Ataxia; Epilepsies, Myoclonic; G(M1) Ganglioside; Galactosidases; Hexoses; Humans; Liver; Lysosomes; Male; Mucolipidoses; Mucopolysaccharidoses; Polysaccharides; Skin; Skin Manifestations; Spinal Cord; Syndrome

1977
The transport of lysosomal enzymes.
    Journal of supramolecular structure, 1977, Volume: 6, Issue:1

    Topics: Biological Transport; Cells, Cultured; Fibroblasts; Hexoses; Humans; Hydrolases; Iduronidase; Immune Sera; Kinetics; Lysosomes; Mucolipidoses

1977