Page last updated: 2024-08-20

3-o-methylglucose and Carbohydrate Metabolism, Inborn Error

3-o-methylglucose has been researched along with Carbohydrate Metabolism, Inborn Error in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (20.00)	18.2507
2000's	4 (80.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
De Vivo, DC; Engelstad, K; Fujii, T; Ma, L; Pascual, JM; Shi, L; Wang, D; Yang, H	1
Lehrman, MA; Shang, J	1
De Vivo, DC; Engelstad, K; Jhung, S; Pascual, JM; Sun, RP; Wang, D; Yang, H	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; Garcia-Alvarez, M; Ho, YY; Klepper, J; O'Driscoll, KR; Parides, MK; Wang, D	1

Trials

1 trial(s) available for 3-o-methylglucose and Carbohydrate Metabolism, Inborn Error

Article	Year
Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects. Annals of neurology, 2005, Volume: 57, Issue:1 Topics: 3-O-Methylglucose; Adolescent; Blood Glucose; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diet Therapy; DNA Mutational Analysis; Electroencephalography; Exons; Female; Glucose; Glucose Transporter Type 1; Humans; Infant; Ketoses; Lactic Acid; Male; Monosaccharide Transport Proteins; Mutation; Phenotype; Polymorphism, Genetic	2005

Article

Year

Glut-1 deficiency syndrome: clinical, genetic, and therapeutic aspects.

Annals of neurology, 2005, Volume: 57, Issue:1

Topics: 3-O-Methylglucose; Adolescent; Blood Glucose; Brain; Carbohydrate Metabolism, Inborn Errors; Child; Child, Preschool; Diet Therapy; DNA Mutational Analysis; Electroencephalography; Exons; Female; Glucose; Glucose Transporter Type 1; Humans; Infant; Ketoses; Lactic Acid; Male; Monosaccharide Transport Proteins; Mutation; Phenotype; Polymorphism, Genetic

2005

Other Studies

4 other study(ies) available for 3-o-methylglucose and Carbohydrate Metabolism, Inborn Error

Article	Year
Functional studies of the T295M mutation causing Glut1 deficiency: glucose efflux preferentially affected by T295M. Pediatric research, 2008, Volume: 64, Issue:5 Topics: 3-O-Methylglucose; Adolescent; Animals; Carbohydrate Metabolism, Inborn Errors; Child; Erythrocytes; Female; Gene Transfer Techniques; Genotype; Glucose Transporter Type 1; Humans; Kinetics; Male; Models, Molecular; Mutation, Missense; Phenotype; Protein Conformation; Structure-Activity Relationship; Xenopus laevis	2008
Metformin-stimulated mannose transport in dermal fibroblasts. The Journal of biological chemistry, 2004, Mar-12, Volume: 279, Issue:11 Topics: 3-O-Methylglucose; Biological Transport; Carbohydrate Metabolism, Inborn Errors; Cells, Cultured; Deoxyglucose; Dose-Response Relationship, Drug; Fibroblasts; Glucose; Glycosylation; Humans; Hypoglycemic Agents; Lipid Metabolism; Mannose; Metformin; Models, Biological; Monosaccharide Transport Proteins; Phloretin; Phlorhizin; Skin; Time Factors; Tunicamycin	2004
Seizures, ataxia, developmental delay and the general paediatrician: glucose transporter 1 deficiency syndrome. Journal of paediatrics and child health, 2006, Volume: 42, Issue:5 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
Erythrocyte 3-O-methyl-D-glucose uptake assay for diagnosis of glucose-transporter-protein syndrome. Journal of clinical laboratory analysis, 1999, Volume: 13, Issue:3 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