acetoacetic acid has been researched along with Muscular Dystrophy, Duchenne in 1 studies
acetoacetic acid : A 3-oxo monocarboxylic acid that is butyric acid bearing a 3-oxo substituent.
Muscular Dystrophy, Duchenne: An X-linked recessive muscle disease caused by an inability to synthesize DYSTROPHIN, which is involved with maintaining the integrity of the sarcolemma. Muscle fibers undergo a process that features degeneration and regeneration. Clinical manifestations include proximal weakness in the first few years of life, pseudohypertrophy, cardiomyopathy (see MYOCARDIAL DISEASES), and an increased incidence of impaired mentation. Becker muscular dystrophy is a closely related condition featuring a later onset of disease (usually adolescence) and a slowly progressive course. (Adams et al., Principles of Neurology, 6th ed, p1415)
| Excerpt | Relevance | Reference |
|---|---|---|
| "An emaciated patient suffering from Duchenne Muscular Dystrophy and volume depletion presented with acidosis of unknown origin." | 1.33 | Unexplained acidosis of malnutrition: a study by ion-exchange chromatography/mass spectrometry. ( Forni, LG; Hilton, PJ; Lord, GA; McKinnon, W; Peron, JM, 2006) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hilton, PJ | 1 |
| McKinnon, W | 1 |
| Lord, GA | 1 |
| Peron, JM | 1 |
| Forni, LG | 1 |
1 other study available for acetoacetic acid and Muscular Dystrophy, Duchenne
| Article | Year |
|---|---|
Unexplained acidosis of malnutrition: a study by ion-exchange chromatography/mass spectrometry.
Topics: Acetoacetates; Acidosis; Adolescent; Chromatography, High Pressure Liquid; Chromatography, Ion Excha | 2006 |