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

3-hydroxyglutaric acid and carnitine

3-hydroxyglutaric acid has been researched along with carnitine in 7 studies

Compound Research Comparison

Studies
(3-hydroxyglutaric acid)		Trials
(3-hydroxyglutaric acid)		Recent Studies (post-2010)
(3-hydroxyglutaric acid)		Studies
(carnitine)		Trials
(carnitine)		Recent Studies (post-2010) (carnitine)
831219,6257503,016

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's5 (71.43)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Corral, I; Gimeno, A; Martínez Castrillo, JC; Martínez-Pardo, M1
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
Gutman, A; Jakobs, C; Korman, SH; Wanders, RJ; Waterham, HR1
Crnic, LR; Fricker, G; Goodman, SI; Harding, CO; Hoffmann, GF; Hörster, F; Koeller, DM; Kölker, S; Mahringer, A; Mühlhausen, C; Müller, I; Okun, JG; Sauer, SW1
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

7 other study(ies) available for 3-hydroxyglutaric acid and carnitine

ArticleYear
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
    Neurologia (Barcelona, Spain), 2001, Volume: 16, Issue:8

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases, Metabolic; Carnitine; Fibroblasts; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Magnetic Resonance Imaging; Movement Disorders; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Riboflavin; Tomography, X-Ray Computed

2001
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
Novel metabolic and molecular findings in hepatic carnitine palmitoyltransferase I deficiency.
    Molecular genetics and metabolism, 2005, Volume: 86, Issue:3

    Topics: Adult; Carnitine; Carnitine O-Palmitoyltransferase; Child, Preschool; Dicarboxylic Acids; Female; Glutarates; Humans; Infant; Male; Mutation; Palmitates

2005
Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood-brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency.
    Journal of neurochemistry, 2006, Volume: 97, Issue:3

    Topics: Amino Acids; Animals; Biological Transport; Blood-Brain Barrier; Blotting, Western; Brain; Carnitine; Cells, Cultured; Dicarboxylic Acids; Disease Models, Animal; Endothelial Cells; Glucose; Glutarates; Glutaryl-CoA Dehydrogenase; Heart; Liver; Mice; Mice, Inbred C57BL; Mice, Knockout; Models, Biological; Muscles; Neurodegenerative Diseases; Risk Factors; Statistics, Nonparametric; Swine; Time Factors; Tissue Distribution

2006
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