creatine has been researched along with Autosomal Dominant Optic Atrophy in 1 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Recently, the clinical spectrum of dominant optic atrophy has been extended to frequent syndromic forms, exhibiting various degrees of neurological and muscle impairments frequently found in mitochondrial diseases." | 1.38 | The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse. ( Angebault, C; Bielicki, G; Boddaert, N; Brabet, P; Cazevieille, C; Chaix, B; Delettre, C; Gueguen, N; Hamel, CP; Lenaers, G; Mausset-Bonnefont, AL; Puel, JL; Renou, JP; Reynier, P; Rigau, V; Sarzi, E; Seveno, M; Wang, J, 2012) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Sarzi, E | 1 |
| Angebault, C | 1 |
| Seveno, M | 1 |
| Gueguen, N | 1 |
| Chaix, B | 1 |
| Bielicki, G | 1 |
| Boddaert, N | 1 |
| Mausset-Bonnefont, AL | 1 |
| Cazevieille, C | 1 |
| Rigau, V | 1 |
| Renou, JP | 1 |
| Wang, J | 1 |
| Delettre, C | 1 |
| Brabet, P | 1 |
| Puel, JL | 1 |
| Hamel, CP | 1 |
| Reynier, P | 1 |
| Lenaers, G | 1 |
1 other study available for creatine and Autosomal Dominant Optic Atrophy
| Article | Year |
|---|---|
The human OPA1delTTAG mutation induces premature age-related systemic neurodegeneration in mouse.
Topics: Acoustic Stimulation; Age Factors; Aging, Premature; Animals; Aspartic Acid; Chi-Square Distribution | 2012 |