fucose has been researched along with Lipid Metabolism, Inborn Error in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 15 (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 |
---|---|
Dawson, G; Tsay, GC | 1 |
Atkins, L; Kanfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE | 1 |
Berman, ER; Kohn, G; Stein, H; Yatziv, S | 1 |
Brady, RO | 2 |
Den Tandt, WR; Giesberts, MA | 1 |
Robinson, D | 1 |
Blümcke, S; Freitag, F; Küchemann, K | 1 |
Brady, RO; de Webster, HF; Hogan, EL; Matthieu, JM; Quarles, RH | 1 |
Berra, B; Brunngraber, EG; Di Palma, S | 1 |
Brady, RO; Matthieu, JM; Quarles, RH | 1 |
Cotlier, E; Hindman, J | 1 |
Montreuil, J; Strecker, G | 1 |
Dacremont, G; Kint, JA | 1 |
Dawson, G; Spranger, JW | 1 |
3 review(s) available for fucose and Lipid Metabolism, Inborn Error
Article | Year |
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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 |
12 other study(ies) available for fucose and Lipid Metabolism, Inborn Error
Article | Year |
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Glycopeptide storage in fibroblasts from patients with inborn errors of glycoprotein and glycosphingolipid catabolism.
Topics: alpha-L-Fucosidase; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fibroblasts; Fucose; Galactose; Galactosidases; Glucosamine; Glycopeptides; Hexosaminidases; Humans; Lipid Metabolism, Inborn Errors; Mannose; Mannosidases; Metabolism, Inborn Errors; Sialic Acids; Skin | 1975 |
Acid hydrolase deficiencies and abnormal glycoproteins in mucolipidosis. 3 (pseudo-Hurler polydystrophy).
Topics: Chromatography, Ion Exchange; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Fucose; Galactosamine; Glucuronidase; Glycoproteins; Glycoside Hydrolases; Humans; Hydrolases; Leukocytes; Lipid Metabolism, Inborn Errors; Mucopolysaccharidosis I; Neuraminic Acids; Proteinuria; Skin; Sulfuric Acids; Uronic Acids | 1974 |
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 |
Deficiency of lysosomal enzymes in storage diseases.
Topics: Acetates; Acid Phosphatase; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Female; Fucose; Galactosidases; Glucuronidase; Glycolipids; Glycosaminoglycans; Glycoside Hydrolases; Hexosaminidases; Humans; Hydrolases; Infant; Intellectual Disability; Leukocytes; Lipid Metabolism, Inborn Errors; Liver; Lysosomes; Male; Middle Aged; Mucopolysaccharidoses; Sulfatases | 1973 |
Hepatic ultrastructure in fucosidosis.
Topics: Biopsy; Brain Diseases; Capillaries; Cerebral Decortication; Child, Preschool; Epithelium; Fucose; Histiocytes; Humans; Inclusion Bodies; Intellectual Disability; Lipid Metabolism, Inborn Errors; Liver; Male; Microscopy, Electron | 1971 |
Characterization of the fraction obtained from the CNS of Jimpy mice by a procedure for myelin isolation.
Topics: Aging; Animals; Brain; Carbon Radioisotopes; Cell Fractionation; Cell Membrane; Cerebrosides; Chromatography, Thin Layer; Electrophoresis, Polyacrylamide Gel; Fucose; Galactose; Glycoproteins; Lipid Metabolism, Inborn Errors; Lipoproteins; Mice; Mice, Inbred Strains; Microscopy, Electron; Mutation; Myelin Sheath; Nerve Tissue Proteins; Nucleotides, Cyclic; Phosphoric Diester Hydrolases; Tritium | 1974 |
Altered levels of tissue gangliosides and glycoproteins in the infantile form of GM1-gangliosidosis.
Topics: Brain; Cerebrosides; Chromatography, Thin Layer; Female; Fucose; Galactose; Galactosidases; Gangliosides; Glycoproteins; Hexosamines; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Liver; Lung; Male; Mannose; Phospholipids; Spleen; Sulfoglycosphingolipids | 1974 |
Anomalies of myelin-associated glycoproteins in 'Quaking' mice.
Topics: Animals; Carbon Radioisotopes; Centrifugation, Density Gradient; Electrophoresis, Polyacrylamide Gel; Fucose; Glycoproteins; Indicators and Reagents; Isotope Labeling; Lipid Metabolism, Inborn Errors; Mice; Mice, Inbred Strains; Molecular Weight; Muscle Proteins; Mutation; Myelin Sheath; Spectrophotometry; Time Factors; Tritium | 1974 |
Glycosidases in normal human leukocytes and abnormalities in G M1 -gangliosidosis.
Topics: Adolescent; Adult; Aged; Carrier State; Child; Clinical Enzyme Tests; Female; Fucose; Galactosidases; Glycoside Hydrolases; Heterozygote; Hexosaminidases; Homozygote; Humans; Infant; Leukocytes; Lipid Metabolism, Inborn Errors; Male; Mannose; Middle Aged | 1972 |
[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 |
ABO blood groups and lysosomal diseases.
Topics: ABO Blood-Group System; Fucose; Glycolipids; Humans; Lipid Metabolism, Inborn Errors; Lysosomes | 1971 |
Fucosidosis: a glycosphingolipidosis.
Topics: Fucose; Glycolipids; Humans; Lipid Metabolism, Inborn Errors; Sphingolipids | 1971 |