3-hydroxy-3-methylglutaryl-coenzyme a has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| León Guijarro, JL; Muñoz-Bonet, JI; Ortega-Sánchez, MD | 1 |
| Anikster, Y; Bernardini, I; Burgess, HA; Ciccone, C; Dorward, H; Feldman, B; Huizing, M; Kelley, RI; Kratz, LE; Pei, W; Sood, R; Yokogawa, T | 1 |
| Yoshida, I | 1 |
1 review(s) available for 3-hydroxy-3-methylglutaryl-coenzyme a and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
[3-Hydroxy-3-methylglutaryl-CoA-lyase deficiency].
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Diagnosis, Differential; Humans; Leucine; Meglutol; Mutation; Prognosis | 1998 |
2 other study(ies) available for 3-hydroxy-3-methylglutaryl-coenzyme a and Amino Acid Metabolism Disorders, Inborn
| Article | Year |
|---|---|
Management and long-term evolution of a patient with 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency.
Topics: Acetyl-CoA C-Acetyltransferase; Acyl Coenzyme A; Adolescent; Amino Acid Metabolism, Inborn Errors; Blood Glucose; Brain; Disease Management; Electroencephalography; Follow-Up Studies; Forecasting; Glucose; Humans; Hypoglycemia; Infusions, Intravenous; Magnetic Resonance Imaging; Male; Tomography, X-Ray Computed | 2017 |
A model of Costeff Syndrome reveals metabolic and protective functions of mitochondrial OPA3.
Topics: Acyl Coenzyme A; Alleles; Amino Acid Metabolism, Inborn Errors; Animals; Disease Models, Animal; Electron Transport; Glutarates; Membrane Proteins; Mitochondria; Models, Biological; Models, Genetic; Optic Atrophy; Phosphorylation; Proteins; Zebrafish; Zebrafish Proteins | 2010 |