adenine has been researched along with Chronic Progressive External Ophthalmoplegia in 3 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "The patients with MELAS had lower mutation levels as well as a lower proportion of RRF, and these two parameters were even lower in the PEO and MDM patients." | 1.31 | Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes. ( Akita, Y; Iwanaga, R; Kato, H; Koga, A; Koga, Y; Matsuishi, T; Sato, Y; Takane, N; Tubone, J, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Spinazzola, A | 1 |
| Carrara, F | 2 |
| Mora, M | 2 |
| Zeviani, M | 2 |
| Tiranti, V | 1 |
| Confalonieri, P | 1 |
| Maffei, RM | 1 |
| Lamantea, E | 1 |
| Koga, Y | 1 |
| Koga, A | 1 |
| Iwanaga, R | 1 |
| Akita, Y | 1 |
| Tubone, J | 1 |
| Matsuishi, T | 1 |
| Takane, N | 1 |
| Sato, Y | 1 |
| Kato, H | 1 |
3 other studies available for adenine and Chronic Progressive External Ophthalmoplegia
| Article | Year |
|---|---|
Mitochondrial myopathy and ophthalmoplegia in a sporadic patient with the 5698G-->A mitochondrial DNA mutation.
Topics: Adenine; Aged; Base Sequence; Chronic Disease; DNA, Mitochondrial; Electron Transport Complex IV; Gu | 2004 |
A novel mutation (8342G-->A) in the mitochondrial tRNA(Lys) gene associated with progressive external ophthalmoplegia and myoclonus.
Topics: Adenine; Adult; Autoanalysis; Base Sequence; Epilepsies, Myoclonic; Female; Guanine; Humans; Molecul | 1999 |
Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes.
Topics: Adenine; Adult; Child; Diabetes Mellitus; DNA, Mitochondrial; Guanine; Humans; Leigh Disease; MELAS | 2000 |