mannose has been researched along with Syndrome in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (50.00) | 18.7374 |
| 1990's | 3 (37.50) | 18.2507 |
| 2000's | 1 (12.50) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Endo, T; Manya, H | 1 |
| Alessi, DM; Benitez, JT; Cunningham, JG; Dade, AW; Jones, MZ; Lovell, KL; Mostosky, UV; Vorro, JR | 1 |
| Buist, N; Diaz, S; Freeze, H; Manzi, A; Paneerselvam, K; Powell, LD; Varki, A; Vij, R | 1 |
| Alton, G; Freeze, HH; Harms, E; Harms, HK; Hasilik, M; Koch, HG; Körner, C; Marquardt, T; Niehues, R; Reiter, K; Schiebe-Sukumar, M; von Figura, K; Wu, R; Zimmer, KP | 1 |
| Pitkänen, E; Pitkänen, OM; Vanhanen, H | 1 |
| Hedo, JA; Moncada, VY; Serrano-Rios, M; Taylor, SI | 1 |
| Miller, CS; Reynolds, LW; Taylor, HA; Thomas, GH | 1 |
| Häger, A; Hallgren, P; Hansson, G; Henriksson, KG; Lundblad, A; Svensson, S | 1 |
1 review(s) available for mannose and Syndrome
| Article | Year |
|---|---|
[Defective O-mannosyl glycosylation causes congenital muscular dystrophies].
Topics: Abnormalities, Multiple; Animals; Brain; Dystroglycans; Eye Abnormalities; Glycosylation; Humans; Mannose; Mannosyltransferases; Muscular Dystrophies; Mutation; N-Acetylglucosaminyltransferases; Syndrome | 2004 |
7 other study(ies) available for mannose and Syndrome
| Article | Year |
|---|---|
Caprine beta-mannosidosis: clinical and pathological features.
Topics: Animals; Brain; Carbohydrate Metabolism, Inborn Errors; Female; Goats; Male; Mannose; Mannosidases; Pedigree; Syndrome | 1983 |
Carbohydrate-deficient glycoprotein syndrome: not an N-linked oligosaccharide processing defect, but an abnormality in lipid-linked oligosaccharide biosynthesis?
Topics: Blood Proteins; Carbohydrates; Cell Line; Female; Glycoproteins; Glycosylation; Humans; Isoelectric Focusing; Lipid Metabolism; Mannose; Oligosaccharides; Syndrome; Transferrin | 1994 |
Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.
Topics: Cells, Cultured; Glycoproteins; Glycosylation; Humans; Infant; Male; Mannose; Mannose-6-Phosphate Isomerase; Mutation; Protein Processing, Post-Translational; Protein-Losing Enteropathies; Syndrome; Transferrin | 1998 |
Metabolic syndrome is associated with changes in D-mannose metabolism.
Topics: Aged; Blood Glucose; Body Mass Index; Cholesterol; Diabetes Mellitus, Type 2; Female; Glucose Intolerance; Humans; Hyperlipidemias; Hypertension; Male; Mannose; Obesity; Syndrome; Triglycerides; Uric Acid | 1999 |
Insulin-receptor biosynthesis in cultured lymphocytes from an insulin-resistant patient (Rabson-Mendenhall syndrome). Evidence for defect before insertion of receptor into plasma membrane.
Topics: Cell Membrane; Cells, Cultured; Humans; Insulin Resistance; Lymphocytes; Mannose; Methionine; Protein Precursors; Radioligand Assay; Receptor, Insulin; Syndrome | 1986 |
Mucolipidosis 3 (Pseudo-Hurler polydystrophy): multiple lysosomal enzyme abnormalities in serum and cultured fibroblast cells.
Topics: Acetamides; Cells, Cultured; Electrophoresis, Starch Gel; Fibroblasts; Fucose; Galactosidases; Glycoside Hydrolases; Hexosaminidases; Humans; In Vitro Techniques; Lysosomes; Mannose; Methods; Mucopolysaccharidosis I; Skin; Spectrophotometry; Sulfatases; Syndrome; Temperature | 1973 |
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 |