mannose has been researched along with Liver Dysfunction in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 1 (16.67) | 2.80 |
Authors | Studies |
---|---|
Maeda, H | 1 |
Aiello, C; Barone, R; Bertini, E; Carella, M; Concolino, D; Fiumara, A; Foulquier, F; Garozzo, D; Jaeken, J; Lefeber, DJ; Matthijs, G; Mercuri, E; Messina, S; Morava, E; Passarelli, C; Race, V; Riemersma, M; Santorelli, F; Sturiale, L; Vleugels, W; Wevers, RA | 1 |
Cretz, M; de Keyzer, Y; de Lonlay, P; Galmiche, L; Jaubert, F; Kuster, A; Lacaille, F; Mention, K; Romano, S; Seta, N; Valayannopoulos, V; Zaidan, H | 1 |
Besmond, C; Feingold, J; Gabolde, M; Guilloud-Bataille, M; Hubert, D; Lenaerts, C | 1 |
Rose, IA; Warms, JV | 1 |
Adachi, F; Phillips, MJ; Yu, DT | 1 |
6 other study(ies) available for mannose and Liver Dysfunction
Article | Year |
---|---|
[Albumin-based Drug Delivery System Targeting Mannose Receptors and Its Application to Medical Treatments].
Topics: Albumins; Animals; Drug Carriers; Drug Delivery Systems; Humans; Inflammation; Interferon-alpha; Liver Diseases; Mannose; Mannose Receptor; Mice; Neoplasms; Receptors, Albumin | 2023 |
DPM2-CDG: a muscular dystrophy-dystroglycanopathy syndrome with severe epilepsy.
Topics: Adolescent; Adult; Aged; Child; Child, Preschool; Coagulation Protein Disorders; Congenital Disorders of Glycosylation; DNA Mutational Analysis; Drug Resistance; Dystroglycans; Electromyography; Endoplasmic Reticulum; Epilepsy; Female; Fibroblasts; Glycosylation; Humans; Infant; Isoelectric Focusing; Liver Diseases; Male; Mannose; Mannosyltransferases; Microcephaly; Middle Aged; Molecular Sequence Data; Muscular Dystrophies; Mutation; Mutation, Missense; Pregnancy; Vision Disorders; Young Adult | 2012 |
Development of liver disease despite mannose treatment in two patients with CDG-Ib.
Topics: Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Disease Progression; Female; Follow-Up Studies; Glycosylation; Humans; Liver; Liver Diseases; Mannose; Treatment Failure | 2008 |
The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.
Topics: Alleles; Carrier Proteins; Chi-Square Distribution; Chronic Disease; Collectins; Cystic Fibrosis; Female; Genetic Predisposition to Disease; Genotype; Humans; Liver Diseases; Male; Mannose; Mutation; Odds Ratio; Phenotype; Sex Distribution | 2001 |
Glucose- and mannose-1,6-P2 as activators of phosphofructokinase in red blood cells.
Topics: Alkalosis; Arabinose; Carbohydrate Metabolism, Inborn Errors; Chromatography, Ion Exchange; Enzyme Activation; Erythrocytes; Glucosephosphates; Glyceraldehyde-3-Phosphate Dehydrogenases; Hexosediphosphates; Humans; Hydrogen-Ion Concentration; In Vitro Techniques; Iodoacetates; Kinetics; Liver Diseases; Mannose; Phosphofructokinase-1; Pyruvate Kinase; Ribose; Sugar Alcohols | 1974 |
An ultrastructural study of fructose-induced hepatic cell injury. Comparison of human and experimental lesions.
Topics: Animals; Biopsy; Carbohydrate Metabolism, Inborn Errors; Chemical and Drug Induced Liver Injury; Disease Models, Animal; Endoplasmic Reticulum; Fructose; Galactose; Glucose; Glycogen; Golgi Apparatus; Humans; Liver; Liver Diseases; Male; Mannitol; Mannose; Microscopy; Microscopy, Electron; Rats; Rats, Inbred Strains; Ribosomes | 1972 |