glutaric acid has been researched along with Diseases, Metabolic in 11 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
| Excerpt | Relevance | Reference |
|---|---|---|
| "We report three cases of L-2-hydroxyglutaric acidemia and three cases of Canavan disease." | 7.69 | Clinical and magnetic resonance imaging features of L-2-hydroxyglutaric acidemia: report of three cases in comparison with Canavan disease. ( Aktan, G; Erdem, G; Jacobs, C; Renda, Y; Saatçi, I; Schutgens, RB; Simşek, A; Topçu, M; Wanders, RJ, 1996) |
| " Antiquitin deficiency is the most common form of pyridoxine-dependent epilepsy." | 5.05 | Inherited Disorders of Lysine Metabolism: A Review. ( Bouchereau, J; Schiff, M, 2020) |
| "Due to the importance of early detection of metabolic diseases in newborns, it is essential to measure organoacids; L-Tryptophan, Sebacic acid, and Glutaric acid in very low concentrations." | 4.31 | Application of sensitive SERS plasmonic biosensor for high detection of metabolic disorders. ( Aboltaman, R; Cheraghi, A; Kiamehr, Z; Malekfar, R, 2023) |
| "We report three cases of L-2-hydroxyglutaric acidemia and three cases of Canavan disease." | 3.69 | Clinical and magnetic resonance imaging features of L-2-hydroxyglutaric acidemia: report of three cases in comparison with Canavan disease. ( Aktan, G; Erdem, G; Jacobs, C; Renda, Y; Saatçi, I; Schutgens, RB; Simşek, A; Topçu, M; Wanders, RJ, 1996) |
| "The glutaric acidurias are a group of inborn errors of metabolism with different etiologies." | 1.62 | Glutaric aciduria type 3 is a naturally occurring biochemical trait in inbred mice of 129 substrains. ( Argmann, C; Bender, A; Dodatko, T; Houten, SM; Leandro, J; Yu, C, 2021) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (18.18) | 18.7374 |
| 1990's | 2 (18.18) | 18.2507 |
| 2000's | 4 (36.36) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 3 (27.27) | 2.80 |
| Authors | Studies |
|---|---|
| Aboltaman, R | 1 |
| Kiamehr, Z | 1 |
| Cheraghi, A | 1 |
| Malekfar, R | 1 |
| Bouchereau, J | 1 |
| Schiff, M | 1 |
| Leandro, J | 1 |
| Bender, A | 1 |
| Dodatko, T | 1 |
| Argmann, C | 1 |
| Yu, C | 1 |
| Houten, SM | 1 |
| Oguz, KK | 1 |
| Ozturk, A | 1 |
| Cila, A | 1 |
| Beresford, MW | 1 |
| Pourfarzam, M | 1 |
| Davidson, JE | 1 |
| Bal, D | 1 |
| Kraska-Dziadecka, A | 1 |
| Gradowska, W | 1 |
| Gryff-Keller, A | 1 |
| Topçu, M | 1 |
| Erdem, G | 1 |
| Saatçi, I | 1 |
| Aktan, G | 1 |
| Simşek, A | 1 |
| Renda, Y | 1 |
| Schutgens, RB | 2 |
| Wanders, RJ | 1 |
| Jacobs, C | 1 |
| Monavari, AA | 1 |
| Naughten, ER | 1 |
| Amir, N | 1 |
| el-Peleg, O | 1 |
| Gross, V | 1 |
| Turnbull, DM | 1 |
| Bartlett, K | 1 |
| Eyre, JA | 1 |
| Gardner-Medwin, D | 1 |
| Johnson, MA | 1 |
| Fisher, J | 1 |
| Watmough, NJ | 1 |
| de Visser, M | 1 |
| Scholte, HR | 1 |
| Bolhuis, PA | 1 |
| Luyt-Houwen, IE | 1 |
| Vaandrager-Verduin, MH | 1 |
| Veder, HA | 1 |
| Oey, PL | 1 |
1 review available for glutaric acid and Diseases, Metabolic
| Article | Year |
|---|---|
Inherited Disorders of Lysine Metabolism: A Review.
Topics: 2-Aminoadipic Acid; Aldehyde Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Arginine; Brain; B | 2020 |
10 other studies available for glutaric acid and Diseases, Metabolic
| Article | Year |
|---|---|
Application of sensitive SERS plasmonic biosensor for high detection of metabolic disorders.
Topics: Aluminum; Biosensing Techniques; Humans; Infant, Newborn; Metabolic Diseases; Metal Nanoparticles; S | 2023 |
Glutaric aciduria type 3 is a naturally occurring biochemical trait in inbred mice of 129 substrains.
Topics: Acyltransferases; Amino Acid Metabolism, Inborn Errors; Animals; Disease Models, Animal; Glutarates; | 2021 |
Diffusion-weighted MR imaging and MR spectroscopy in glutaric aciduria type 1.
Topics: Brain; Diffusion Magnetic Resonance Imaging; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; | 2005 |
"So doctor, what exactly is wrong with my muscles? Glutaric aciduria type II presenting in a teenager".
Topics: Adolescent; Confidentiality; Glutarates; Humans; Metabolic Diseases; Molecular Biology; Muscular Dis | 2006 |
Investigation of a wide spectrum of inherited metabolic disorders by 13C NMR spectroscopy.
Topics: Biomarkers; Canavan Disease; Glutarates; Hemiterpenes; Humans; Lactic Acid; Magnetic Resonance Spect | 2008 |
Clinical and magnetic resonance imaging features of L-2-hydroxyglutaric acidemia: report of three cases in comparison with Canavan disease.
Topics: Canavan Disease; Cerebellar Nuclei; Child; Child, Preschool; Female; Glutarates; Humans; Magnetic Re | 1996 |
Prevention of cerebral palsy in glutaric aciduria type 1 by dietary management.
Topics: Adolescent; Adult; Biomarkers; Cerebral Palsy; Child; Family Health; Glutarates; Humans; Magnetic Re | 2000 |
Opercular sign: significance beyond cerebral dysgenesis.
Topics: Brain; Child, Preschool; Glutarates; Humans; Infant; Infant, Newborn; Metabolic Diseases | 1990 |
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.
Topics: Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Glycine; Humans; Infant; Lipid Metabolism | 1988 |
Riboflavin-responsive lipid-storage myopathy and glutaric aciduria type II of early adult onset.
Topics: Adolescent; Carnitine; Child; Fatty Acids; Female; Fibroblasts; Glutarates; Humans; Infant; Lipid Me | 1986 |