glutaric acid has been researched along with Metabolic Diseases 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.
Metabolic Diseases: Generic term for diseases caused by an abnormal metabolic process. It can be congenital due to inherited enzyme abnormality (METABOLISM, INBORN ERRORS) or acquired due to disease of an endocrine organ or failure of a metabolically important organ such as the liver. (Stedman, 26th ed)
| 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 Metabolic Diseases
| 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 Metabolic Diseases
| 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 |