galactose has been researched along with Acid beta-Glucosidase Deficiency in 20 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 19 (95.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (5.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Kolter, T; Wendeler, M | 1 |
| Berra, B; Brunngraber, EG; Davis, LG; Javaid, JI | 1 |
| de Vries, A; Klibansky, C; Matoth, Y; Ossimi, Z; Pinkhas, J | 1 |
| Brady, RO; Gal, AE; Quirk, JM; Tokoro, T; Weis, AL | 1 |
| Brady, RO | 3 |
| Glew, RH; Lee, RE | 1 |
| Friedman, RB; Kanfer, JN | 1 |
| González-Sastre, F; Pampols, T; Sabater, J | 1 |
| Heinrich, E; Kaiser, E | 1 |
| Samuelsson, B; Samuelsson, K | 1 |
| Kolman, Z; Michalec, C | 1 |
| Inose, T; Kaneko, Y; Sakai, M; Tano, T | 1 |
| Kennaway, NG; Woolf, LI | 1 |
| Krivit, W; Sweeley, CC; Vance, DE | 1 |
| Bässler, R; Schäfer, A | 1 |
| AGRANOFF, BW; SUOMI, WD | 1 |
| Minami, R; Nakao, T; Orii, T; Sukegawa, K | 1 |
| Brotz, M; French, JH; Poser, CM | 1 |
4 review(s) available for galactose and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Chemical chaperones--a new concept in drug research.
Topics: 1-Deoxynojirimycin; alpha-Galactosidase; Animals; Enzyme Stability; Fabry Disease; Galactose; Gaucher Disease; Glycoside Hydrolases; Humans; Imino Sugars; Molecular Weight; Piperidines; Protein Conformation; Protein Folding | 2003 |
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 |
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 |
[Biochemistry of Gaucher's disease].
Topics: Cerebrosides; Chromatography, Gas; Galactose; Gaucher Disease; Glycolipids; Histocytochemistry; Humans; Mononuclear Phagocyte System | 1968 |
16 other study(ies) available for galactose and Acid beta-Glucosidase Deficiency
| Article | Year |
|---|---|
Accumulation of lactosyl ceramide in leukocytes of patients with adult Gaucher's disease.
Topics: Adult; Aged; Cerebrosides; Child; Female; Galactose; Gaucher Disease; Glucose; Glycosphingolipids; Humans; Lactose; Leukocytes; Male; Middle Aged | 1976 |
Animal and cellular models of sphingolipid storage disorders of humans.
Topics: Animals; Brain; Cerebrosides; Disease Models, Animal; Galactose; Galactosylceramidase; Galactosylceramides; Gaucher Disease; Glucosylceramides; Humans; Intestine, Small; Leukodystrophy, Globoid Cell; Rats; Rats, Inbred Strains | 1986 |
The adnormal biochemistry of inherited disorders of lipid metabolism.
Topics: Brain; Ceramides; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Female; Fibroblasts; Galactose; Galactosidases; Gaucher Disease; Glucose; Glycolipids; Glycoside Hydrolases; Hexosaminidases; Humans; Intestines; Kidney; Leukocytes; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Muscles; Niemann-Pick Diseases; Phosphoric Diester Hydrolases; Sphingomyelins; Spleen; Sulfoglycosphingolipids; Syndrome | 1973 |
Composition of the membranous deposits occurring in Gaucher's disease.
Topics: Adolescent; Centrifugation, Density Gradient; Cerebrosides; Cholesterol; Chromatography, Thin Layer; Electrophoresis, Disc; Female; Freeze Etching; Galactose; Gaucher Disease; Glycoproteins; Hexosamines; Humans; Membranes; Microscopy, Electron; Molecular Weight; Neuraminic Acids; Peptides; Phospholipids; Pronase; Proteins; Sodium Dodecyl Sulfate; Spleen | 1973 |
Composition of sialoglycans isolated from Gaucher's spleen.
Topics: Adolescent; Arabinose; Chromatography, DEAE-Cellulose; Chromatography, Gas; Chromatography, Ion Exchange; Female; Fucose; Galactose; Gaucher Disease; Glucose; Glycopeptides; Hexosamines; Humans; Mannose; Neuraminic Acids; Spleen; Xylose | 1974 |
Infantile Gaucher's disease: A biochemical study.
Topics: Acute Disease; Brain; Brain Chemistry; Brain Stem; Cerebellum; Cerebrosides; Cholesterol; Chromatography, Thin Layer; Female; Frontal Lobe; Galactose; Gangliosides; Gaucher Disease; Glucose; Humans; Infant; Infant, Newborn; Lipid Metabolism; Lipoproteins; Male; Phosphatidylcholines; Phosphatidylethanolamines; Phospholipids; Sphingomyelins; Sulfoglycosphingolipids; Temporal Lobe | 1974 |
Gas-liquid chromatography-mass spectrometry of cerebrosides as trimethylsilyl ether derivatives.
Topics: Cerebrosides; Chemical Phenomena; Chemistry; Chromatography, Gas; Ethers; Fatty Acids; Galactose; Gaucher Disease; Glycolipids; Glycosides; Hexoses; Humans; Methods; Silicon; Spectrum Analysis; Spleen | 1969 |
Biochemistry of sphingolipids. XV. An improved semiquantitative paper chromatographic method of gluco- and galactocerebrosides.
Topics: Adult; Brain Chemistry; Cerebrosides; Chromatography, Paper; Galactose; Gaucher Disease; Glucose; Humans; Infant; Liver; Methods; Spleen | 1967 |
[Biochemical analysis of glycolipids in the brain tissue in Gaucher's disease].
Topics: Brain; Caproates; Chromatography, Gas; Galactose; Gaucher Disease; Glucose; Glycolipids; Humans | 1967 |
Splenic lipids in Gaucher's disease.
Topics: Adolescent; Adult; Amino Acids; Carbohydrate Metabolism; Cerebrosides; Child; Child, Preschool; Chromatography; Chromatography, Thin Layer; Colorimetry; Freezing; Galactose; Gaucher Disease; Glucose; Glycolipids; Glycosides; Humans; Infant; Lipid Metabolism; Lipidoses; Methods; Middle Aged; Preservation, Biological; Spleen | 1968 |
Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis.
Topics: Adolescent; Adult; Cerebrosides; Child; Erythrocytes; Female; Galactose; Gaucher Disease; Glucose; Heterozygote; Humans; Lactose; Lipidoses; Male; Middle Aged | 1969 |
[Pathomorphogenesis of kerasin deposits in Gaucher's disease. Light and electron microscopic studies of liver and spleen].
Topics: Adult; Brain; Female; Galactose; Gaucher Disease; Humans; Liver; Microscopy; Microscopy, Electron; Spleen | 1966 |
LIPIDS OF THE SPLEEN IN GAUCHER'S DISEASE.
Topics: Cerebrosides; Chromatography; Fatty Acids; Gaucher Disease; Glycolipids; Hexoses; Humans; Lipid Metabolism; Lipids; Spleen | 1965 |
Hyperglycopeptiduria in genetic mucolipidoses.
Topics: Child; Child, Preschool; Chromatography, Paper; Female; Gangliosides; Gaucher Disease; Glycopeptides; Glycosaminoglycans; Hexoses; Humans; Infant; Lipidoses; Male; Mucopolysaccharidoses; Mucopolysaccharidosis IV; Neuraminic Acids; Sphingolipids; Sulfates; Uronic Acids | 1974 |
Metabolic disorders of sphingolipid metabolism in man.
Topics: Amino Alcohols; Carbon Isotopes; Cerebrosides; Diffuse Cerebral Sclerosis of Schilder; Esterases; Fatty Acids; Gangliosides; Gaucher Disease; Glycols; Hexoses; Humans; Lipid Metabolism; Lipidoses; Niemann-Pick Diseases; Sphingomyelins; Sulfuric Acids | 1970 |
Cerebral lipid composition in infantile Gaucher's disease (IGD).
Topics: Cerebral Cortex; Cerebrosides; Chromatography, Paper; Chromatography, Thin Layer; Gaucher Disease; Hexoses; Humans; Infant; Infant, Newborn | 1968 |