Compounds > 3-o-methylglucose

Page last updated: 2024-08-20

3-o-methylglucose and Developmental Disabilities

3-o-methylglucose has been researched along with Developmental Disabilities in 4 studies

Research

Studies (4)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (50.00)	18.2507
2000's	2 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
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
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
Behmand, RA; De Vivo, DC; Harik, SI; Jacobson, RI; Ronen, GM; Trifiletti, RR	1

Other Studies

4 other study(ies) available for 3-o-methylglucose and Developmental Disabilities

Article	Year
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
Defective glucose transport across brain tissue barriers: a newly recognized neurological syndrome. Neurochemical research, 1999, Volume: 24, Issue:4 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
Autosomal dominant glut-1 deficiency syndrome and familial epilepsy. Annals of neurology, 2001, Volume: 50, Issue:4 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
Defective glucose transport across the blood-brain barrier as a cause of persistent hypoglycorrhachia, seizures, and developmental delay. The New England journal of medicine, 1991, Sep-05, Volume: 325, Issue:10 Topics: 3-O-Methylglucose; Adult; Biological Transport; Blood Glucose; Blood-Brain Barrier; Child, Preschool; Cytochalasin B; Developmental Disabilities; Erythrocyte Membrane; Female; Glucose; Humans; Infant, Newborn; Male; Methylglucosides; Monosaccharide Transport Proteins; Psychomotor Performance; Seizures	1991