glutaric acid has been researched along with Acidosis in 9 studies
glutaric acid: RN given refers to parent cpd
glutaric acid : An alpha,omega-dicarboxylic acid that is a linear five-carbon dicarboxylic acid.
Acidosis: A pathologic condition of acid accumulation or depletion of base in the body. The two main types are RESPIRATORY ACIDOSIS and metabolic acidosis, due to metabolic acid build up.
Excerpt | Relevance | Reference |
---|---|---|
"Riboflavin and carnitine treatment corrected the metabolic abnormalities and she improved clinically." | 1.28 | Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult. ( Bell, RB; Brownell, AK; Engel, AG; Frerman, FE; Goodman, SI; Roe, CR; Seccombe, DW; Snyder, FF, 1990) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 6 (66.67) | 18.2507 |
2000's | 2 (22.22) | 29.6817 |
2010's | 1 (11.11) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Liu, H | 1 |
Miao, JK | 1 |
Yu, CW | 1 |
Wan, KX | 1 |
Zhang, J | 1 |
Yuan, ZJ | 1 |
Yang, J | 1 |
Wang, DJ | 1 |
Zeng, Y | 1 |
Zou, L | 1 |
Kölker, S | 1 |
Hoffmann, GF | 1 |
Schor, DS | 1 |
Feyh, P | 1 |
Wagner, L | 1 |
Jeffrey, I | 1 |
Pourfarzam, M | 1 |
Okun, JG | 1 |
Zschocke, J | 1 |
Baric, I | 1 |
Bain, MD | 1 |
Jakobs, C | 1 |
Chalmers, RA | 1 |
Wendel, U | 1 |
Bakkeren, J | 1 |
de Jong, J | 1 |
Bongaerts, G | 1 |
Hostetler, MA | 1 |
Arnold, GL | 1 |
Mooney, R | 1 |
Bennett, MJ | 1 |
Rinaldo, P | 1 |
Roe, CR | 2 |
al-Essa, MA | 1 |
Rashed, MS | 1 |
Bakheet, SM | 1 |
Patay, ZJ | 1 |
Ozand, PT | 1 |
Indo, Y | 1 |
Glassberg, R | 1 |
Yokota, I | 1 |
Tanaka, K | 1 |
Medlock, MD | 1 |
Rhead, WJ | 1 |
Pollack, L | 1 |
Meredith, JT | 1 |
Pearl, G | 1 |
Reece, C | 1 |
Kamiya, M | 1 |
Eimoto, T | 1 |
Kishimoto, H | 1 |
Tsudzuki, T | 1 |
Morishita, H | 1 |
Wada, Y | 1 |
Wakabayashi, T | 1 |
Hashimoto, T | 1 |
Goodman, SI | 2 |
Frerman, FE | 2 |
Bell, RB | 1 |
Brownell, AK | 1 |
Engel, AG | 1 |
Seccombe, DW | 1 |
Snyder, FF | 1 |
9 other studies available for glutaric acid and Acidosis
Article | Year |
---|---|
Severe clinical manifestation of mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency associated with two novel mutations: a case report.
Topics: Acidosis; Acyl Coenzyme A; Adipates; Carnitine; Diarrhea; Dicarboxylic Acids; Exome Sequencing; Fata | 2019 |
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 Anal | 2003 |
Glutaric aciduria mediated by gut bacteria.
Topics: Acidosis; Bacteria; Child, Preschool; Digestive System; Fibroblasts; Glutarates; Glutaryl-CoA Dehydr | 1995 |
Hypoketotic hypoglycemic coma in a 21-month-old child.
Topics: Acidosis; Age of Onset; Algorithms; Amino Acid Metabolism, Inborn Errors; Coma; Decision Trees; Diag | 1999 |
Glutaric aciduria type II: observations in seven patients with neonatal- and late-onset disease.
Topics: Acidosis; Age of Onset; Brain; Carnitine; Child; Consanguinity; Female; Glutarates; Humans; Infant; | 2000 |
Molecular characterization of variant alpha-subunit of electron transfer flavoprotein in three patients with glutaric acidemia type II--and identification of glycine substitution for valine-157 in the sequence of the precursor, producing an unstable matur
Topics: Acidosis; Base Sequence; Blotting, Northern; Cell Line; Electron-Transferring Flavoproteins; Flavopr | 1991 |
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a sibling.
Topics: Acidosis; Cerebral Hemorrhage; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Fetal Di | 1991 |
Glutaric aciduria type II: autopsy study of a case with electron-transferring flavoprotein dehydrogenase deficiency.
Topics: Acidosis; Electron Transport; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Glutarate | 1990 |
Electron transfer flavoprotein: ubiquinone oxidoreductase (ETF:QO) deficiency in an adult.
Topics: Acidosis; Adult; Carnitine; Electron-Transferring Flavoproteins; Fatty Acid Desaturases; Female; Glu | 1990 |