Trevisson, E.
Città della Speranza Foundation
2 papers on CoChatORCID 0000-0002-5380-6265
Most cited papers
- Verified
A functionally dominant mitochondrial DNA mutation
Sacconi, S., Salviati, L., Nishigaki, Y., Walker, W. F., Hernandez-Rosa, E., Trevisson, E., Delplace, S., Desnuelle, C., Shanske, S., Hirano, M., et al. (2008) · Human Molecular Genetics
Mitochondrial Function and PathologyMetabolism and Genetic Disorders
Cited by 113
- Verified
Secondary Coenzyme Q 10 Deficiencies in Oxidative Phosphorylation (OXPHOS) and Non-OXPHOS Disorders
Yubero, D., Montero, R., Martín, M. A., Montoya, J., Ribes, A., Grazina, M., Trevisson, E., Rodriguez-Aguilera, J. C., Hargreaves, I. P., Salviati, L., et al. (2016) · Mitochondrion
Coenzyme Q10 studies and effectsMitochondrial Function and Pathology
Cited by 72
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