| Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation F Longo, S Benedetti, AA Zambon, MGN Sora, C Di Resta, D De Ritis, ... Human Molecular Genetics 29 (2), 177-188, 2020 | 37 | 2020 |
| Assessment of sacsin turnover in patients with ARSACS: implications for molecular diagnosis and pathogenesis F Longo, D De Ritis, A Miluzio, D Fraticelli, J Baets, M Scarlato, ... Neurology 97 (23), e2315-e2327, 2021 | 14 | 2021 |
| Restoring calcium homeostasis in Purkinje cells arrests neurodegeneration and neuroinflammation in the ARSACS mouse model A Del Bondio, F Longo, D De Ritis, E Spirito, P Podini, B Brais, A Bachi, ... JCI insight 8 (12), 2023 | 5 | 2023 |
| Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5 CA Franchino, M Brughera, V Baderna, D De Ritis, A Rocco, S Seneca, ... Brain 147 (3), 1043, 2024 | | 2024 |
| Unraveling the physiopathological role of sacsin, the protein mutated in autosomal recessive spastic ataxia of Charlevoix–Saguenay (ARSACS) D DE RITIS Università Vita-Salute San Raffaele, 2023 | | 2023 |
| Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay F Longo, D De Ritis, A Miluzio, D Fraticelli, J Baets, M Scarlato, ... bioRxiv, 2021.03. 16.435646, 2021 | | 2021 |
