carnitine has been researched along with Retinitis Pigmentosa in 1 studies
Retinitis Pigmentosa: Hereditary, progressive degeneration of the retina due to death of ROD PHOTORECEPTORS initially and subsequent death of CONE PHOTORECEPTORS. It is characterized by deposition of pigment in the retina.
| 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 |
|---|---|
| Park, HD | 1 |
| Kim, SR | 1 |
| Ki, CS | 1 |
| Lee, SY | 1 |
| Chang, YS | 1 |
| Jin, DK | 1 |
| Park, WS | 1 |
1 other study available for carnitine and Retinitis Pigmentosa
| Article | Year |
|---|---|
Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.
Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Carnitine; DNA Mutational Analysis; Humans; Infa | 2009 |