3-o-methylglucose has been researched along with Aura in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Fischbarg, J; Gertsen, E; Klepper, J; Salas-Burgos, A | 1 |
| Brockmann, K; De Vivo, DC; Fischbarg, J; Hanefeld, F; Ho, YY; Korenke, CG; Kranz-Eble, P; Kuang, K; Ma, L; Pascual, JM; von Moers, A; Wang, D; Yang, H | 1 |
2 other study(ies) available for 3-o-methylglucose and Aura
| Article | Year |
|---|---|
Bench meets bedside: a 10-year-old girl and amino acid residue glycine 75 of the facilitative glucose transporter GLUT1.
Topics: 3-O-Methylglucose; Amino Acid Sequence; Child; Epilepsy; Female; Glycine; Humans; Models, Molecular; Molecular Sequence Data; Mutation, Missense; Syndrome | 2005 |
Autosomal dominant glut-1 deficiency syndrome and familial epilepsy.
Topics: 3-O-Methylglucose; Amino Acid Sequence; Animals; Child; Developmental Disabilities; Epilepsy; Erythrocytes; Family Health; Female; Genes, Dominant; Glucose Transporter Type 1; Humans; Infant, Newborn; Male; Middle Aged; Molecular Sequence Data; Monosaccharide Transport Proteins; Mutation, Missense; Oocytes; Pedigree; Xenopus laevis | 2001 |