fucose has been researched along with Cherry Red Spot Myoclonus Syndrome in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (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 |
|---|---|
| Yamashita, K | 1 |
| Sewell, AC | 1 |
| Federico, A; Guazzi, G | 1 |
| Aula, P; Ekblom, P; Laurila, P; Nordling, S; Raivio, KO; Virtanen, I | 1 |
| Cambier, PH; Ginsel, LA | 1 |
| Staal, GE; Straks, W; Troost, J; Willemse, J | 1 |
| Hultberg, B | 1 |
| Van Hoof, F | 1 |
3 review(s) available for fucose and Cherry Red Spot Myoclonus Syndrome
| Article | Year |
|---|---|
[Metabolic disorders of glycoproteins in congenital glycosidase deficiencies].
Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Paper; Fucose; G(M1) Ganglioside; Gangliosidoses; Glucosidases; Glycoproteins; Humans; Lactose Intolerance; Mannose; Mucolipidoses; Mucopolysaccharidoses; Neuraminidase; Oligosaccharides; Sandhoff Disease | 1984 |
Urinary oligosaccharides in lysosomal and other metabolic disorders.
Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Chromatography, Thin Layer; Fucose; Glycogen Storage Disease; Humans; Mannose; Marfan Syndrome; Mass Screening; Metabolism, Inborn Errors; Mucolipidoses; Oligosaccharides; Osteogenesis Imperfecta; Sandhoff Disease; Tay-Sachs Disease | 1982 |
Mucopolysaccharidoses and mucolipidoses.
Topics: beta-Galactosidase; Cells, Cultured; Child, Preschool; Chondroitin Sulfates; Female; Fucose; Gangliosidoses; Genetic Carrier Screening; Hexosyltransferases; Humans; Iduronidase; Liver; Lysosomes; Mannose; Mucolipidoses; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III; Mucopolysaccharidosis IV; Mucopolysaccharidosis VI | 1974 |
5 other study(ies) available for fucose and Cherry Red Spot Myoclonus Syndrome
| Article | Year |
|---|---|
Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.
Topics: Aspartylglucosaminuria; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography, Thin Layer; Fucose; Gangliosidoses; Germany, West; Glycogen; Glycogen Storage Disease; Glycolipids; Glycoproteins; Humans; Infant; Mannosidases; Mass Screening; Mucolipidoses; Oligosaccharides | 1980 |
Characterization of storage material in cultured fibroblasts by specific lectin binding in lysosomal storage diseases.
Topics: Carbohydrate Metabolism, Inborn Errors; Fibroblasts; Fluorescent Dyes; Fucose; Glucose; Histocytochemistry; Humans; Lectins; Lysosomes; Mannose; Mucolipidoses | 1980 |
Fucosidosis and I-cell disease: a fine structural and silver-staining study of abnormal inclusion bodies in small-intestinal cells.
Topics: Adolescent; alpha-L-Fucosidase; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Child; Child, Preschool; Female; Fibroblasts; Fucose; Glycoproteins; Glycosaminoglycans; Golgi Apparatus; Humans; Inclusion Bodies; Infant; Intestine, Small; Lipids; Lymphocytes; Lysosomes; Male; Mucolipidoses; Silver; Staining and Labeling; Vacuoles | 1978 |
[Fucosidosis].
Topics: alpha-L-Fucosidase; Fabry Disease; Fucose; Humans; Mucolipidoses | 1977 |
Metabolism of mannose and fucose in cultured fibroblasts from patients with mannosidosis and mucolipidosis.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fibroblasts; Fucose; Humans; Mannose; Mucolipidoses | 1979 |