fucose has been researched along with Sphingolipid Storage Diseases in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (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 |
|---|---|
| Gura, C; Kopyść, Z; Ryzko, J | 1 |
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
2 review(s) available for fucose and Sphingolipid Storage Diseases
| Article | Year |
|---|---|
[Fucosidosis].
Topics: Abnormalities, Multiple; Age Factors; alpha-L-Fucosidase; Body Weight; Brain; Child; Child, Preschool; Cytoplasm; Diagnosis, Differential; Female; Fucose; Glycolipids; Glycoproteins; Humans; Infant; Male; Prenatal Diagnosis; Prognosis; Sphingolipidoses | 1975 |
Glycoprotein catabolism in brain tissue in the lysosomal enzyme deficiency diseases.
Topics: Adolescent; Binding Sites; Brain; Child; Concanavalin A; Fucose; Galactose; Gangliosidoses; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Infant, Newborn; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Middle Aged; Protein Binding; Sialic Acids; Sphingolipidoses | 1976 |