galactose has been researched along with Niemann-Pick Diseases in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 11 (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 |
|---|---|
| Brady, RO | 3 |
| Carton, D; Cocquyt, G; Dacremont, G; Kint, JA | 1 |
| Hiatt, W; Sattler, M; Wenger, DA | 1 |
| Kawamura, N | 1 |
| Fredrickson, DS; Jacobson, CB; Sloan, HR; Uhlendorf, BW | 1 |
| O'Brien, JS; Okada, S | 1 |
| Berra, B; Brunngraber, EG; Zambotti, V | 1 |
| Debuch, H; Kannan, R; Tjiong, HB; Wiedemann, HR | 1 |
| Booth, DA; Cumings, JN; Goodwin, H | 1 |
1 review(s) available for galactose and Niemann-Pick Diseases
| Article | Year |
|---|---|
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 |
10 other study(ies) available for galactose and Niemann-Pick Diseases
| Article | Year |
|---|---|
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 |
Glucosylceramide in plasma of patients with Niemann-Pick disease.
Topics: Cerebrosides; Chromatography; Chromatography, Thin Layer; Galactose; Glucose; Humans; Lactose; Niemann-Pick Diseases; Silicon Dioxide; Sphingomyelins | 1974 |
Globoid cell leukodystrophy: deficiency of lactosyl ceramide beta-galactosidase.
Topics: Adult; Brain; Ceramides; Female; Galactose; Galactosidases; Gangliosides; Humans; Infant; Lactose; Leukodystrophy, Globoid Cell; Leukodystrophy, Metachromatic; Lipidoses; Liver; Male; Niemann-Pick Diseases; Skin; Spleen; Syndrome | 1974 |
Hepatic and splenic glycolipids in a case of Niemann-Pick disease.
Topics: Amino Alcohols; Chromatography, Gas; Chromatography, Thin Layer; Disaccharides; Fatty Acids; Galactose; Glucose; Glycolipids; Glycols; Humans; Infant; Infrared Rays; Liver; Male; Niemann-Pick Diseases; Spectrophotometry; Sphingomyelins; Spleen | 1971 |
Beta-galactosidase in tissue culture derived from human skin and bone marrow. Enzyme defect in GM1 gangliosidosis.
Topics: Biopsy; Bone Marrow; Bone Marrow Cells; Brain; Culture Media; Culture Techniques; Fibroblasts; Galactose; Galactosidases; Gangliosides; Glycolipids; Humans; Infant; Intellectual Disability; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Niemann-Pick Diseases; Rheumatic Heart Disease; Skin | 1969 |
Generalized gangliosidosis: beta-galactosidase deficiency.
Topics: Acid Phosphatase; Aged; Brain; Carbon Isotopes; Child; Child, Preschool; Chromatography, Paper; Galactose; Galactosidases; Gangliosides; Glucosidases; Glycosides; Humans; Infant; Kidney; Lipid Metabolism, Inborn Errors; Lipidoses; Liver; Male; Middle Aged; Molecular Biology; Niemann-Pick Diseases; Nitrophenols; Spleen; Uracil Nucleotides | 1968 |
Altered levels of tissue glycoproteins, gangliosides, glycosaminoglycans and lipids in Niemann-Pick's disease.
Topics: Brain Chemistry; Cell Membrane; Cellulose; Child, Preschool; Cholesterol; Chromatography, Gel; Chromatography, Ion Exchange; Chromatography, Paper; Chromatography, Thin Layer; Electrophoresis; Gangliosides; Glucosamine; Glycoproteins; Glycosaminoglycans; Hexoses; Humans; Infant; Lipids; Liver; Neuraminic Acids; Niemann-Pick Diseases; Phospholipids; Sphingomyelins | 1973 |
Unusual glycolipids in brain cortex of a visceral lipidosis (Niemann-Pick disease?).
Topics: Brain Chemistry; Ceramides; Cerebral Cortex; Cerebrosides; Child; Cholesterol; Chromatography; Chromatography, Gas; Chromatography, Thin Layer; Fatty Acids; Female; Gangliosides; Glycolipids; Hexoses; Humans; Lipidoses; Lipids; Male; Niemann-Pick Diseases; Sulfoglycosphingolipids | 1974 |
Abnormal gangliosides in Tay-Sachs disease, Niemann-Pick's disease, and gargoylism.
Topics: Amino Alcohols; Brain Chemistry; Cerebral Cortex; Chromatography, Thin Layer; Gangliosides; Hexosamines; Hexoses; Humans; Lipidoses; Mucopolysaccharidoses; Neuraminic Acids; Niemann-Pick Diseases; Sphingomyelins | 1966 |
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 |