Page last updated: 2024-10-15

alpha-hydroxyglutarate and Autosomal Chromosome Disorders

alpha-hydroxyglutarate has been researched along with Autosomal Chromosome Disorders in 2 studies

2-hydroxyglutarate : A dicarboxylic acid anion obtained by deprotonation of at least one of the carboxy groups of 2-hydroxyglutaric acid.
2-hydroxyglutaric acid : A 2-hydroxydicarboxylic acid that is glutaric acid in which one hydrogen alpha- to a carboxylic acid group is substituted by a hydroxy group.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Craigen, WJ1
Jakobs, C1
Sekul, EA1
Levy, ML1
Gibson, KM1
Butler, IJ1
Herman, GE1
Eeg-Olofsson, O1
Zhang, WW1
Olsson, Y1
Jagell, S1
Hagenfeldt, L1

Other Studies

2 other studies available for alpha-hydroxyglutarate and Autosomal Chromosome Disorders

ArticleYear
D-2-hydroxyglutaric aciduria in neonate with seizures and CNS dysfunction.
    Pediatric neurology, 1994, Volume: 10, Issue:1

    Topics: Basal Ganglia Diseases; Blindness; Brain Diseases, Metabolic; Chromosome Aberrations; Chromosome Dis

1994
D-2-hydroxyglutaric aciduria with cerebral, vascular, and muscular abnormalities in a 14-year-old boy.
    Journal of child neurology, 2000, Volume: 15, Issue:7

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Atrophy; Brain; Chromosome Aberrations; Chromosome

2000