glutaric acid has been researched along with alpha-hydroxyglutarate in 5 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bennett, MJ; Curnock, DA; Engel, PC; Gray, RG; Hull, D; Patrick, AD; Pollitt, RJ; Shaw, L | 1 |
| Coe, CJ; Lee, JS; Yoon, HR | 1 |
| Brooks, R; Gutman, A; Jakobs, C; Korman, SH; Salomons, GS | 1 |
| Bal, D; Gradowska, W; Gryff-Keller, A; Kraska-Dziadecka, A | 1 |
| Brauburger, K; Burckhardt, BC; Burckhardt, G | 1 |
5 other study(ies) available for glutaric acid and alpha-hydroxyglutarate
| Article | Year |
|---|---|
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatally.
Topics: Adipates; Carbon Dioxide; Fatty Acid Desaturases; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant, Newborn; Liver; Lysine; Pregnancy; Prenatal Diagnosis; Sarcosine | 1984 |
A Korean girl with alpha-aminoadipic and alpha-ketoadipic aciduria accompanied with elevation of 2-hydroxyglutarate and glutarate.
Topics: 2-Aminoadipic Acid; Adipates; Amino Acid Metabolism, Inborn Errors; Diet, Protein-Restricted; Female; Gas Chromatography-Mass Spectrometry; Glutarates; Humans; Infant; Korea | 2001 |
D-2-hydroxyglutaric aciduria and glutaric aciduria type 1 in siblings: coincidence, or linked disorders?
Topics: Brain Diseases, Metabolic, Inborn; Child, Preschool; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Male; Mutation; Oxidoreductases Acting on CH-CH Group Donors; Siblings | 2004 |
Investigation of a wide spectrum of inherited metabolic disorders by 13C NMR spectroscopy.
Topics: Biomarkers; Canavan Disease; Glutarates; Hemiterpenes; Humans; Lactic Acid; Magnetic Resonance Spectroscopy; Metabolic Diseases; Models, Chemical; Orotic Acid; Pentanoic Acids; Phenylketonurias; Pyrrolidonecarboxylic Acid; Tyrosinemias; Urinalysis | 2008 |
The sodium-dependent di- and tricarboxylate transporter, NaCT, is not responsible for the uptake of D-, L-2-hydroxyglutarate and 3-hydroxyglutarate into neurons.
Topics: Animals; Biological Transport; Electrophysiology; Glutarates; Humans; Kidney; Kinetics; Neurons; Oocytes; Patch-Clamp Techniques; RNA, Complementary; Symporters; Transcription, Genetic; Xenopus laevis | 2011 |