DI MEO, IVANO
DI MEO, IVANO
Universita' degli Studi di MILANO
Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases
2024 C. Cavestro, F. Morra, A. Legati, M. D'Amato, A. Nasca, A. Iuso, N. Lubarr, J.L. Morrison, P.G. Wheeler, C. Serra-Juhé, B. Rodríguez-Santiago, E. Turón-Viñas, C. Prouteau, M. Barth, S.J. Hayflick, D. Ghezzi, V. Tiranti, I. Di Meo
Gene Therapy for Mitochondrial Diseases: Current Status and Future Perspective
2022 A. Di Donfrancesco, G. Massaro, I. DI MEO, V. Tiranti, E. Bottani, D. Brunetti
A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy
2021 A. Nasca, I. Di Meo, Y. Fellig, A. Saada, O. Elpeleg, D. Ghezzi, S. Edvardson
Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions
2020 S. Marchet, A. Legati, A. Nasca, I. Di Meo, M. Spagnolo, N. Zanetti, E. Lamantea, A. Catania, C. Lamperti, D. Ghezzi
| Titolo | Data di pubblicazione | Autori | Tipo | File | Abstract |
|---|---|---|---|---|---|
| Emerging variants, unique phenotypes, and transcriptomic signatures: an integrated study of COASY-associated diseases | 2024 | Nasca, AlessiaGhezzi, DanieleDi Meo, Ivano + | Article (author) | - | |
| Gene Therapy for Mitochondrial Diseases: Current Status and Future Perspective | 2022 | Ivano Di MeoDario Brunetti + | Article (author) | - | |
| A novel homozygous MSTO1 mutation in Ashkenazi Jewish siblings with ataxia and myopathy | 2021 | Di Meo I.Ghezzi D. + | Article (author) | - | |
| Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions | 2020 | Di Meo I.Lamantea E.Lamperti C.Ghezzi D. + | Article (author) | - |