3-o-methylglucose has been researched along with Syndrome in 9 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (11.11) | 18.7374 |
1990's | 2 (22.22) | 18.2507 |
2000's | 5 (55.56) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
De Vivo, DC; Fujii, T; Ho, YY; Law, PP; Morimoto, M; Wang, D; Yoshioka, H | 1 |
Fischbarg, J; Flörcken, A; Klepper, J; Voit, T | 1 |
Fischbarg, J; Gertsen, E; Klepper, J; Salas-Burgos, A | 1 |
Appleton, DB; Bowling, FG; Burke, CJ; Coman, DJ; De Vivo, DC; McGill, JJ; O'Neil, CM; Pelekanos, JT; Sinclair, KG; Wallace, GB; Wang, D | 1 |
De Vivo, DC; Fischbarg, J; Jarjour, IT; Klepper, J; O'Driscoll, KR; Vera, JC; Wang, D | 1 |
De Vivo, DC; Garcia-Alvarez, M; Ho, YY; Klepper, J; O'Driscoll, KR; Parides, MK; Wang, D | 1 |
De Vivo, DC; Fischbarg, J; Ho, YY; Klepper, J; Wang, D; Yang, H | 1 |
Buhl, ES; Flyvbjerg, A; Jessen, N; Ledet, T; Lund, S; Pedersen, O; Pedersen, SB; Pold, R; Schmitz, O | 1 |
Elsas, LJ; Griffin, LD; Langley, S; Longo, N; Shuster, RC | 1 |
9 other study(ies) available for 3-o-methylglucose and Syndrome
Article | Year |
---|---|
T295M-associated Glut1 deficiency syndrome with normal erythrocyte 3-OMG uptake.
Topics: 3-O-Methylglucose; Adolescent; Child; Erythrocytes; Female; Glucose Transporter Type 1; Humans; Male; Mutation; Phenotype; Syndrome | 2011 |
Effects of anticonvulsants on GLUT1-mediated glucose transport in GLUT1 deficiency syndrome in vitro.
Topics: 3-O-Methylglucose; Adolescent; Adult; Anticonvulsants; Biological Transport; Blood-Brain Barrier; Child; Child, Preschool; Erythrocytes; Ethanol; Female; Glucose Transporter Type 1; Humans; In Vitro Techniques; Infant; Male; Middle Aged; Monosaccharide Transport Proteins; Seizures; Syndrome | 2003 |
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 |
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome.
Topics: 3-O-Methylglucose; Anticonvulsants; Ataxia; Brain Diseases, Metabolic, Inborn; Carbohydrate Metabolism, Inborn Errors; Child; Developmental Disabilities; Diet Therapy; Female; Glucose Transporter Type 1; Humans; Infant; Lumbar Vertebrae; Male; Seizures; Spinal Puncture; Syndrome; Treatment Outcome | 2006 |
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 |
Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome.
Topics: 3-O-Methylglucose; Adolescent; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Erythrocytes; Female; Glucose Transporter Type 1; Humans; Infant; Ketosis; Male; Monosaccharide Transport Proteins; Mutation; ROC Curve; Sensitivity and Specificity; Syndrome | 1999 |
Glucose transporter type 1 deficiency syndrome (Glut1DS): methylxanthines potentiate GLUT1 haploinsufficiency in vitro.
Topics: 3-O-Methylglucose; Adolescent; Caffeine; Case-Control Studies; Child; Erythrocytes; Female; Humans; In Vitro Techniques; Kinetics; Male; Monosaccharide Transport Proteins; Mutation; Phenobarbital; Syndrome; Theophylline | 2001 |
Long-term AICAR administration reduces metabolic disturbances and lowers blood pressure in rats displaying features of the insulin resistance syndrome.
Topics: 3-O-Methylglucose; Adenylate Kinase; Aminoimidazole Carboxamide; Animals; Blood Glucose; Blood Pressure; Glucose Clamp Technique; Glucose Transporter Type 4; Hypertension; Insulin Resistance; Male; Metabolic Syndrome; Monosaccharide Transport Proteins; Muscle Proteins; Rats; Rats, Zucker; Ribonucleotides; Syndrome | 2002 |
Increased glucose transport by human fibroblasts with a heritable defect in insulin binding.
Topics: 3-O-Methylglucose; Adult; Biological Transport, Active; Cells, Cultured; Child, Preschool; Female; Fibroblasts; Humans; Infant; Insulin-Like Growth Factor I; Male; Metabolism, Inborn Errors; Methylglucosides; Methylglycosides; Monosaccharide Transport Proteins; Receptor, Insulin; Receptors, Cell Surface; Receptors, Somatomedin; Reference Values; RNA, Messenger; Skin; Syndrome | 1989 |