dapi has been researched along with MELAS Syndrome in 1 studies
DAPI: RN given refers to parent cpd.
MELAS Syndrome: A mitochondrial disorder characterized by focal or generalized seizures, episodes of transient or persistent neurologic dysfunction resembling strokes, and ragged-red fibers on muscle biopsy. Affected individuals tend to be normal at birth through early childhood, then experience growth failure, episodic vomiting, and recurrent cerebral insults resulting in visual loss and hemiparesis. The cortical lesions tend to occur in the parietal and occipital lobes and are not associated with vascular occlusion. VASCULAR HEADACHE is frequently associated and the disorder tends to be familial. (From Joynt, Clinical Neurology, 1992, Ch56, p117)
| 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 |
|---|---|
| Kariya, S | 1 |
| Hirano, M | 1 |
| Furiya, Y | 1 |
| Sugie, K | 1 |
| Ueno, S | 1 |
1 other study available for dapi and MELAS Syndrome
| Article | Year |
|---|---|
Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent.
Topics: Adenosine Triphosphatases; bcl-2-Associated X Protein; Cell Line, Tumor; Chaperonin 60; Electron Tra | 2005 |