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411 results

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Page 1
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Aleo SJ, Del Dotto V, Romagnoli M, Fiorini C, Capirossi G, Peron C, Maresca A, Caporali L, Capristo M, Tropeano CV, Zanna C, Ross-Cisneros FN, Sadun AA, Pignataro MG, Giordano C, Fasano C, Cavaliere A, Porcelli AM, Tioli G, Musiani F, Catania A, Lamperti C, Marzoli SB, De Negri A, Cascavilla ML, Battista M, Barboni P, Carbonelli M, Amore G, La Morgia C, Smirnov D, Vasilescu C, Farzeen A, Blickhaeuser B, Prokisch H, Priglinger C, Livonius B, Catarino CB, Klopstock T, Tiranti V, Carelli V, Ghelli AM. Aleo SJ, et al. Among authors: romagnoli m. Cell Rep Med. 2024 Feb 20;5(2):101383. doi: 10.1016/j.xcrm.2023.101383. Epub 2024 Jan 24. Cell Rep Med. 2024. PMID: 38272025 Free PMC article.
Chromatic Pupillometry Findings in Alzheimer's Disease.
Romagnoli M, Stanzani Maserati M, De Matteis M, Capellari S, Carbonelli M, Amore G, Cantalupo G, Zenesini C, Liguori R, Sadun AA, Carelli V, Park JC, La Morgia C. Romagnoli M, et al. Front Neurosci. 2020 Aug 11;14:780. doi: 10.3389/fnins.2020.00780. eCollection 2020. Front Neurosci. 2020. PMID: 32848556 Free PMC article.
Expanding and validating the biomarkers for mitochondrial diseases.
Maresca A, Del Dotto V, Romagnoli M, La Morgia C, Di Vito L, Capristo M, Valentino ML, Carelli V; ER-MITO Study Group. Maresca A, et al. Among authors: romagnoli m. J Mol Med (Berl). 2020 Oct;98(10):1467-1478. doi: 10.1007/s00109-020-01967-y. Epub 2020 Aug 26. J Mol Med (Berl). 2020. PMID: 32851462 Free PMC article.
Therapeutic Options in Hereditary Optic Neuropathies.
Amore G, Romagnoli M, Carbonelli M, Barboni P, Carelli V, La Morgia C. Amore G, et al. Among authors: romagnoli m. Drugs. 2021 Jan;81(1):57-86. doi: 10.1007/s40265-020-01428-3. Drugs. 2021. PMID: 33159657 Free PMC article. Review.
Natural history of patients with Leber hereditary optic neuropathy-results from the REALITY study.
Yu-Wai-Man P, Newman NJ, Carelli V, La Morgia C, Biousse V, Bandello FM, Clermont CV, Campillo LC, Leruez S, Moster ML, Cestari DM, Foroozan R, Sadun A, Karanjia R, Jurkute N, Blouin L, Taiel M, Sahel JA; LHON REALITY Study Group. Yu-Wai-Man P, et al. Eye (Lond). 2022 Apr;36(4):818-826. doi: 10.1038/s41433-021-01535-9. Epub 2021 Apr 28. Eye (Lond). 2022. PMID: 33911213 Free PMC article.
Chromatic Pupillometry in Isolated Rapid Eye Movement Sleep Behavior Disorder.
La Morgia C, Romagnoli M, Pizza F, Biscarini F, Filardi M, Donadio V, Carbonelli M, Amore G, Park JC, Tinazzi M, Carelli V, Liguori R, Plazzi G, Antelmi E. La Morgia C, et al. Among authors: romagnoli m. Mov Disord. 2022 Jan;37(1):205-210. doi: 10.1002/mds.28809. Epub 2021 Oct 7. Mov Disord. 2022. PMID: 34617633 Free PMC article.
Association of rs3027178 polymorphism in the circadian clock gene PER1 with susceptibility to Alzheimer's disease and longevity in an Italian population.
Bacalini MG, Palombo F, Garagnani P, Giuliani C, Fiorini C, Caporali L, Stanzani Maserati M, Capellari S, Romagnoli M, De Fanti S, Benussi L, Binetti G, Ghidoni R, Galimberti D, Scarpini E, Arcaro M, Bonanni E, Siciliano G, Maestri M, Guarnieri B; Italian Multicentric Group on clock genes, actigraphy in AD; Martucci M, Monti D, Carelli V, Franceschi C, La Morgia C, Santoro A. Bacalini MG, et al. Among authors: romagnoli m. Geroscience. 2022 Apr;44(2):881-896. doi: 10.1007/s11357-021-00477-0. Epub 2021 Dec 18. Geroscience. 2022. PMID: 34921659 Free PMC article.
411 results