glutaric acid has been researched along with glutarylcarnitine in 12 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (8.33) | 18.7374 |
| 1990's | 2 (16.67) | 18.2507 |
| 2000's | 5 (41.67) | 29.6817 |
| 2010's | 2 (16.67) | 24.3611 |
| 2020's | 2 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Briones, P; Campistol, J; Christensen, E; Millington, DS; Ribes, A; Riudor, E | 1 |
| Ichiki, T; Kobayashi, M; Nohara, D; Sakuma, T; Sugiyama, N; Wada, Y | 1 |
| Kidouchi, K; Kobayashi, M; Morishita, H; Nohara, D; Sugiyama, N; Wada, Y | 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 |
| Brewster, TG; Cowan, TM; Hahn, SH; Matern, D; Rinaldo, P; Tortorelli, S | 1 |
| Cowan, TM; Enns, GM; Gallagher, RC; Goodman, SI | 1 |
| Cederbaum, SD; Chan, E; Crombez, EA; Goodman, S; Neidich, J; Salazar, D; Spector, E | 1 |
| Alonso, E; Botana, LM; Campbell, K; Chevallier, OP; Duffy, C; Elliott, CT; Graham, SF; Silke, J | 1 |
| Behulova, D; Brennerova, K; Bzduch, V; Chandoga, J; Jurickova, K; Lisyova, J; Petrovic, R; Urbanova, D | 1 |
| Bouchereau, J; Schiff, M | 1 |
| Ahmadzada, S; Aktuglu-Zeybek, C; Kiykim, E; Yalcinkaya, C; Zubarioglu, T | 1 |
1 review(s) available for glutaric acid and glutarylcarnitine
| Article | Year |
|---|---|
Inherited Disorders of Lysine Metabolism: A Review.
Topics: 2-Aminoadipic Acid; Aldehyde Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Arginine; Brain; Brain Diseases, Metabolic; Brain Diseases, Metabolic, Inborn; Carnitine; Epilepsy; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Lysine; Metabolic Diseases; Pyridoxal Phosphate; Pyridoxine | 2020 |
11 other study(ies) available for glutaric acid and glutarylcarnitine
| Article | Year |
|---|---|
Significance of bound glutarate in the diagnosis of glutaric aciduria type I.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Child; Child, Preschool; Gas Chromatography-Mass Spectrometry; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Spectrometry, Mass, Fast Atom Bombardment | 1992 |
Analysis of acylcarnitines in maternal urine for prenatal diagnosis of glutaric aciduria type 2.
Topics: Abortion, Induced; Amino Acid Metabolism, Inborn Errors; Amniotic Fluid; Carnitine; Female; Glutarates; Humans; Pregnancy; Prenatal Diagnosis | 1991 |
Identification of glutarylcarnitine in glutaric aciduria type 1 by carboxylic acid analyzer with an ODS reverse-phase column.
Topics: Acetylcarnitine; Amino Acid Metabolism, Inborn Errors; Autoanalysis; Carboxylic Acids; Carnitine; Chromatography; Glutarates; Humans; Infant; Male | 1987 |
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 |
The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type I.
Topics: Carnitine; Case-Control Studies; Glutarates; Humans | 2005 |
Glutaryl-CoA dehydrogenase deficiency and newborn screening: retrospective analysis of a low excretor provides further evidence that some cases may be missed.
Topics: Carnitine; Cells, Cultured; Fibroblasts; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Mass Spectrometry; Neonatal Screening; Retrospective Studies | 2005 |
Maternal glutaric acidemia, type I identified by newborn screening.
Topics: Amino Acid Metabolism, Inborn Errors; Carnitine; Female; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant, Newborn; Mutation; Neonatal Screening | 2008 |
New insights into the causes of human illness due to consumption of azaspiracid contaminated shellfish.
Topics: Animals; Bivalvia; Carnitine; Cell Line; Cell Line, Tumor; Disease Outbreaks; Foodborne Diseases; Glutarates; HEK293 Cells; Humans; Marine Toxins; Shellfish; Sodium Channels; Spiro Compounds | 2015 |
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 |
COVID-19 triggered encephalopathic crisis in a patient with glutaric aciduria type 1.
Topics: Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Brain Diseases, Metabolic; Carnitine; COVID-19; COVID-19 Testing; Female; Genetic Testing; Glutarates; Glutaryl-CoA Dehydrogenase; Humans; Infant; Magnetic Resonance Imaging; Motor Skills; Movement Disorders; Muscle Hypotonia | 2021 |