3-hydroxybutyric acid has been researched along with MELAS in 2 studies
3-Hydroxybutyric Acid: BUTYRIC ACID substituted in the beta or 3 position. It is one of the ketone bodies produced in the liver.
3-hydroxybutyric acid : A straight-chain 3-hydroxy monocarboxylic acid comprising a butyric acid core with a single hydroxy substituent in the 3- position; a ketone body whose levels are raised during ketosis, used as an energy source by the brain during fasting in humans. Also used to synthesise biodegradable plastics.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The diagnosis of MELAS mutation was reinforced by the absence of an identifiable mutation in the X-linked G4." | 1.31 | Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation). ( Angaroni, C; Argaraña, C; Bacman, S; Civallero, G; De Kremer, RD; Depetris-Boldini, C; Giner-Ayala, A; Gonzalez, I; Guelbert, N; Hliba, E; Johnston, J; Juaneda, E; Kelley, RI; Latini, A; Noher de Halac, I; Oller-Ramírez, A; Paschini-Capra, A; Proujansky, R; Theaux, RA, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Reed, EM | 1 |
| Swanson, AA | 1 |
| Roden, AC | 1 |
| Lin, PT | 1 |
| De Kremer, RD | 1 |
| Paschini-Capra, A | 1 |
| Bacman, S | 1 |
| Argaraña, C | 1 |
| Civallero, G | 1 |
| Kelley, RI | 1 |
| Guelbert, N | 1 |
| Latini, A | 1 |
| Noher de Halac, I | 1 |
| Giner-Ayala, A | 1 |
| Johnston, J | 1 |
| Proujansky, R | 1 |
| Gonzalez, I | 1 |
| Depetris-Boldini, C | 1 |
| Oller-Ramírez, A | 1 |
| Angaroni, C | 1 |
| Theaux, RA | 1 |
| Hliba, E | 1 |
| Juaneda, E | 1 |
2 other studies available for 3-hydroxybutyric acid and MELAS
| Article | Year |
|---|---|
Sudden Unexpected Death in MELAS Syndrome Due to Diabetic Ketoacidosis.
Topics: 3-Hydroxybutyric Acid; Acetone; Adult; Brain; Death, Sudden; Diabetic Ketoacidosis; Glucose; Humans; | 2020 |
Barth's syndrome-like disorder: a new phenotype with a maternally inherited A3243G substitution of mitochondrial DNA (MELAS mutation).
Topics: 3-Hydroxybutyric Acid; Acids; Argentina; Biopsy; Child, Preschool; DNA, Mitochondrial; Electron Tran | 2001 |