Compounds > 3-hydroxyglutaric acid
Page last updated: 2024-09-05

3-hydroxyglutaric acid and glutarylcarnitine

3-hydroxyglutaric acid has been researched along with glutarylcarnitine in 4 studies

Compound Research Comparison

Studies
(3-hydroxyglutaric acid)		Trials
(3-hydroxyglutaric acid)		Recent Studies (post-2010)
(3-hydroxyglutaric acid)		Studies
(glutarylcarnitine)		Trials
(glutarylcarnitine)		Recent Studies (post-2010) (glutarylcarnitine)
8312127012

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bain, MD; Baric, I; Chalmers, RA; Feyh, P; Hoffmann, GF; Jakobs, C; Jeffrey, I; Kölker, S; Okun, JG; Pourfarzam, M; Schor, DS; Wagner, L; Zschocke, J1
Lai, CC; Lee, CC; Lin, WD; Tsai, FJ; Wang, CH1
Goldsher, D; Herskovitz, M; Mandel, H; Sela, BA1
Behulova, D; Brennerova, K; Bzduch, V; Chandoga, J; Jurickova, K; Lisyova, J; Petrovic, R; Urbanova, D1

Other Studies

4 other study(ies) available for 3-hydroxyglutaric acid and glutarylcarnitine

ArticleYear
Glutaryl-CoA dehydrogenase deficiency: region-specific analysis of organic acids and acylcarnitines in post mortem brain predicts vulnerability of the putamen.
    Neuropediatrics, 2003, Volume: 34, Issue:5

    Topics: Acidosis; Acute Disease; Adolescent; Anticonvulsants; Atrophy; Brain; Carnitine; DNA Mutational Analysis; Fatal Outcome; Gas Chromatography-Mass Spectrometry; Gene Expression; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Muscle Hypotonia; N-Methylaspartate; Oxidoreductases Acting on CH-CH Group Donors; Point Mutation; Putamen; Spasm; Vigabatrin

2003
Genetic and biochemical study in a patient with glutaric acidemia type I.
    Journal of the Formosan Medical Association = Taiwan yi zhi, 2004, Volume: 103, Issue:7

    Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child, Preschool; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Mutation; Oxidoreductases Acting on CH-CH Group Donors

2004
Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type I.
    Neurology, 2013, Aug-27, Volume: 81, Issue:9

    Topics: Age of Onset; Amino Acid Metabolism, Inborn Errors; Biological Transport; Brain Diseases, Metabolic; Carnitine; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Male; Middle Aged; Treatment Outcome

2013
GAI - distinct genotype and phenotype characteristics in reported Slovak patients.
    Bratislavske lekarske listy, 2016, Volume: 117, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Base Sequence; Brain Diseases, Metabolic; Carnitine; Early Diagnosis; Female; Gas Chromatography-Mass Spectrometry; Genotype; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Male; Mutation, Missense; Phenotype; Sequence Analysis; Slovakia

2016