dehydroascorbic acid has been researched along with Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (66.67) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chang, CJ; Chen, YT; Cheng, CH; Huang, HY; Lee, YC | 1 |
| De Vivo, DC; Klepper, J; Vera, JC | 1 |
| De Vivo, DC; Fischbarg, J; Jarjour, IT; Klepper, J; O'Driscoll, KR; Vera, JC; Wang, D | 1 |
1 trial(s) available for dehydroascorbic acid and Syndrome
| Article | Year |
|---|---|
Deficient transport of dehydroascorbic acid in the glucose transporter protein syndrome.
Topics: Adult; Ascorbic Acid; Blood-Brain Barrier; Child; Dehydroascorbic Acid; Erythrocytes; Female; Humans; Male; Middle Aged; Monosaccharide Transport Proteins; Oxidation-Reduction; Syndrome | 1998 |
2 other study(ies) available for dehydroascorbic acid and Syndrome
| Article | Year |
|---|---|
Mitochondrial GLUT10 facilitates dehydroascorbic acid import and protects cells against oxidative stress: mechanistic insight into arterial tortuosity syndrome.
Topics: Adipocytes; Animals; Aorta; Arteries; Biological Transport; Cytoprotection; Dehydroascorbic Acid; Gene Expression Profiling; Gene Expression Regulation; Glucose Transport Proteins, Facilitative; Insulin; Mice; Mitochondria; Models, Biological; Myocytes, Smooth Muscle; NIH 3T3 Cells; Organ Specificity; Oxidative Stress; Reactive Oxygen Species; Subcellular Fractions; Syndrome | 2010 |
Defective glucose transport across brain tissue barriers: a newly recognized neurological syndrome.
Topics: 3-O-Methylglucose; Biological Transport; Brain; Child; Dehydroascorbic Acid; Developmental Disabilities; Erythrocytes; Female; Glucose; Glucose Transporter Type 1; Humans; Immunoblotting; Microcephaly; Monosaccharide Transport Proteins; Mutation; Spasms, Infantile; Syndrome | 1999 |