fucose has been researched along with Lipidoses in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (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 |
|---|---|
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
| Atkins, L; Kanfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE | 1 |
| Brady, RO | 2 |
| Brown, BD; Brunngraber, EG; Hof, H | 1 |
| Robinson, D | 1 |
| Touster, O | 1 |
| O'Brien, JS; Veath, ML; Zielke, K | 1 |
| Aro, A; Brown, BD; Brunngraber, EG | 1 |
| Montreuil, J; Strecker, G | 1 |
5 review(s) available for fucose and Lipidoses
| Article | Year |
|---|---|
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 |
Prenatal genetic diagnosis (second of three parts).
Topics: Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Diffuse Cerebral Sclerosis of Schilder; Female; Fetal Diseases; Fibroblasts; Fucose; Galactosemias; Gaucher Disease; Genetic Diseases, Inborn; Glycolipids; Glycosaminoglycans; Humans; Lipid Metabolism, Inborn Errors; Lipidoses; Metabolism, Inborn Errors; Niemann-Pick Diseases; Pregnancy; Refsum Disease; Sulfatases | 1970 |
Disorders of lipid metabolism.
Topics: Adult; Animals; Bone Marrow; Cell Line; Ceramides; Child; Fabry Disease; Fucose; Galactose; Gangliosides; Gaucher Disease; Genetic Variation; Glycolipids; Glycoside Hydrolases; Humans; Leukemia, Myeloid; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipidoses; Mice; Niemann-Pick Diseases; Sulfoglycosphingolipids | 1972 |
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 |
Some aspects of the cellular biochemistry of lysosomal and related glycosidases.
Topics: Animals; Carbohydrate Metabolism, Inborn Errors; Diffuse Cerebral Sclerosis of Schilder; Fucose; Galactosamine; Galactosidases; Gangliosides; Gaucher Disease; Glucosidases; Glucuronidase; Glycoside Hydrolases; Golgi Apparatus; Hexosaminidases; Humans; Hydrogen-Ion Concentration; Isoenzymes; Leukodystrophy, Metachromatic; Lipidoses; Lysosomes; Mannose; Neuraminidase; Serine; Xylose | 1973 |
5 other study(ies) available for fucose and Lipidoses
| Article | Year |
|---|---|
Inborn errors of lipid metabolism.
Topics: Ceramides; Cerebrosides; Fabry Disease; Fucose; Galactosidases; Gaucher Disease; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Humans; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipid Metabolism, Inborn Errors; Lipidoses; Neuraminic Acids; Niemann-Pick Diseases; Organ Specificity; Sphingomyelins; Sulfoglycosphingolipids | 1973 |
Determination of gangliosides, glycoproteins, and glycosaminoglycans in brain tissue.
Topics: Acetates; Adult; Animals; Brain Chemistry; Brain Diseases; Cattle; Cerebral Cortex; Chemical Precipitation; Child; Child, Preschool; Chloroform; Chromatography, Gel; Dialysis; Electrophoresis; Fucose; Galactosemias; Gangliosides; Glycopeptides; Glycoproteins; Glycosaminoglycans; Hexosamines; Hexoses; Humans; Hydrogen-Ion Concentration; Lipidoses; Methanol; Methods; Myelin Sheath; Neuraminic Acids; Papain; Peptide Hydrolases; Pyridinium Compounds; Rats; Solubility; Subacute Sclerosing Panencephalitis; Temperature | 1971 |
Fucosidosis: deficiency of alpha-L-fucosidase in cultured skin fibroblasts.
Topics: Amniocentesis; Amnion; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Cystic Fibrosis; Fibroblasts; Fucose; Glycoside Hydrolases; Humans; In Vitro Techniques; Lipidoses; Male; Mucopolysaccharidoses; Niemann-Pick Diseases; Skin | 1972 |
Glycoproteins in brain tissue of the O-variant of GM2 gangliosidosis.
Topics: Acetamides; Brain; Brain Chemistry; Child, Preschool; Chromatography, Gel; Electrophoresis; Female; Fucose; Galactose; Gangliosides; Glucosamine; Glycoproteins; Hexosamines; Hexosaminidases; Humans; Lipidoses; Male; Mannose; Neuraminic Acids | 1974 |
[Oligosaccharide excretion in a case of GM 2 gangliosidosis due to total N-acetylhexosaminidase deficiency].
Topics: Acetates; Carbohydrate Metabolism, Inborn Errors; Chemical Precipitation; Chromatography; Chromatography, Ion Exchange; Chromatography, Paper; Colorimetry; Ethanol; Fucose; Galactose; Gangliosides; Glucosamine; Glucose; Glycoproteins; Glycoside Hydrolases; Hexosamines; Hexosaminidases; Hexoses; Humans; Infant; Lipid Metabolism, Inborn Errors; Lipidoses; Mannose; Monosaccharides; Neuraminic Acids; Oligosaccharides; Uronic Acids | 1971 |