mannose has been researched along with alpha-Galactosidase A Deficiency in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (75.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Edmunds, T; Honey, D; Hou, L; Kyazike, J; Pan, CQ; Park, A; Stefano, JE; Zhou, Q | 1 |
| Hultberg, B; Sjöblad, S | 1 |
| De Wit-Verbeek, E; Galjaard, H; Hoogeveen, A; Keijzer, W; Vlek-Noot, C | 1 |
| Robinson, D | 1 |
1 review(s) available for mannose and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
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 |
3 other study(ies) available for mannose and alpha-Galactosidase A Deficiency
| Article | Year |
|---|---|
In vitro and in vivo evaluation of a non-carbohydrate targeting platform for lysosomal proteins.
Topics: alpha-Galactosidase; Amino Acid Motifs; Animals; Cell Line, Tumor; Dimerization; Fabry Disease; Female; Half-Life; Humans; Kinetics; Liver; Lysosomes; Male; Mannose; Mice; Mice, Knockout; Oligosaccharides; Peptides; Polyethylene Glycols; Proteins; Rats; Receptor, IGF Type 2; Recombinant Proteins; Tissue Distribution | 2009 |
Lysosomal enzymes in medium from cultured skin fibroblasts from normal individuals and patients with lysosomal diseases.
Topics: Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Fabry Disease; Fibroblasts; Humans; In Vitro Techniques; Lipidoses; Lysosomes; Mannose; Metabolism, Inborn Errors; Mucolipidoses; Mucopolysaccharidosis I; Skin | 1977 |
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 |