carnitine has been researched along with 3-hydroxyglutaric acid in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 5 (71.43) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Corral, I; Gimeno, A; Martínez Castrillo, JC; Martínez-Pardo, M | 1 |
| 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, J | 1 |
| Lai, CC; Lee, CC; Lin, WD; Tsai, FJ; Wang, CH | 1 |
| Gutman, A; Jakobs, C; Korman, SH; Wanders, RJ; Waterham, HR | 1 |
| 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, SW | 1 |
| Goldsher, D; Herskovitz, M; Mandel, H; Sela, BA | 1 |
| Behulova, D; Brennerova, K; Bzduch, V; Chandoga, J; Jurickova, K; Lisyova, J; Petrovic, R; Urbanova, D | 1 |
7 other study(ies) available for carnitine and 3-hydroxyglutaric acid
| Article | Year |
|---|---|
[Glutaric aciduria type I: diagnosis in adulthood and phenotypic variability].
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.
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.
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.
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.
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.
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.
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 |