fucose has been researched along with Glycogenosis in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (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 |
---|---|
Sewell, AC | 1 |
Federico, A; Guazzi, G | 1 |
Robinson, D | 1 |
Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S | 1 |
2 review(s) available for fucose and Glycogenosis
Article | Year |
---|---|
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 |
Multiple forms of glycosidases in the normal and pathological states.
Topics: Carbohydrate Metabolism, Inborn Errors; Chondroitin; Chromatography, Gel; Diffuse Cerebral Sclerosis of Schilder; Fabry Disease; Fucose; Galactosidases; Gangliosides; Gaucher Disease; Glycogen Storage Disease; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Infant; Isoenzymes; Lactose Intolerance; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Mucopolysaccharidoses | 1974 |
2 other study(ies) available for fucose and Glycogenosis
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 |
Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
Topics: Adult; Cardiomyopathies; Chemical Phenomena; Chemistry; Child; Chromatography, Gel; Chromatography, Paper; Electrophoresis; Fucose; Galactose; Glucose; Glucosidases; Glycogen Storage Disease; Humans; Male; Mannose; Methylation; Oligosaccharides; Optical Rotation; Syndrome; Ultrafiltration | 1974 |