mannose has been researched along with Glycogenosis in 9 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 8 (88.89) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (11.11) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Asano, H; Miwa, I; Murata, T; Nagasaka, H; Taguchi, T; Takatani, T; Yorifuji, T | 1 |
| Federico, A; Guazzi, G | 1 |
| Gura, C; Kopyść, Z; Ryzko, J | 1 |
| Kroos, M; Oude Elferink, RP; Reuser, AJ; Tager, JM | 1 |
| De Wit-Verbeek, E; Galjaard, H; Hoogeveen, A; Keijzer, W; Vlek-Noot, C | 1 |
| Robinson, D | 1 |
| Girard, J; Herz, G | 1 |
| Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S | 1 |
| Atkins, L; Kanvfer, JN; Kolodny, EH; Littlefield, JW; Milunsky, A; Shih, VE | 1 |
3 review(s) available for mannose 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 |
Prenatal genetic diagnosis. 3.
Topics: Abortion, Induced; Acid Phosphatase; Adrenal Hyperplasia, Congenital; Amnion; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Congenital Abnormalities; Counseling; Culture Techniques; Cystic Fibrosis; Economics, Medical; Ethics, Medical; Female; Fetal Diseases; Fibroblasts; Genetic Diseases, Inborn; Glycogen Storage Disease; Heterozygote; Homozygote; Humans; Lysosomes; Mannose; Marfan Syndrome; Methods; Mucopolysaccharidoses; Muscular Dystrophies; Porphyrias; Pregnancy; Punctures; Xeroderma Pigmentosum | 1970 |
6 other study(ies) available for mannose and Glycogenosis
| Article | Year |
|---|---|
Low level of fasting plasma mannose in a child with glycogen storage disease type 0 (liver glycogen synthase deficiency).
Topics: Blood Glucose; Case-Control Studies; Child; Child, Preschool; Fasting; Glycogen Storage Disease; Glycogen Synthase; Humans; Liver; Male; Mannose | 2010 |
[Mannosidosis. Asparaginylglucosaminuria].
Topics: Adult; Aminoglycosides; Asparagine; Child, Preschool; Female; Glycogen Storage Disease; Humans; Infant; Male; Mannose; Mannosidases | 1975 |
Defects in synthesis, phosphorylation, and maturation of acid alpha-glucosidase in glycogenosis type II.
Topics: Adolescent; Adult; alpha-Glucosidases; beta-N-Acetylhexosaminidases; Electrophoresis, Polyacrylamide Gel; Fibroblasts; Glucan 1,4-alpha-Glucosidase; Glucosidases; Glycogen Storage Disease; Glycogen Storage Disease Type II; Hexosaminidases; Humans; Infant; Leucine; Male; Mannose; Phosphates; Phosphorylation | 1985 |
The use of quantiatative cytochemical analyses in rapid prenatal detection and somatic cell genetic studies of metabolic diseases.
Topics: Amniocentesis; Amniotic Fluid; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fabry Disease; Female; Galactosidases; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glucosidases; Glycogen Storage Disease; Glycoside Hydrolases; Hexosaminidases; Histocytochemistry; Humans; Hybrid Cells; Mannose; Microchemistry; Pregnancy; Spectrometry, Fluorescence; Uronic Acids | 1974 |
Some aspects of hypoglycemia in pediatrics.
Topics: Acids; Age Factors; Brain Chemistry; Carbohydrate Metabolism, Inborn Errors; Glutamine; Glycogen Storage Disease; Hexoses; Humans; Hypoglycemia; Infant, Newborn; Infant, Newborn, Diseases; Injections, Intravenous; Insulin; Mannose | 1972 |
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 |