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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
2002 3
2003 2
2004 2
2005 1
2006 6
2007 3
2008 6
2009 5
2010 1
2011 6
2012 7
2013 3
2014 6
2015 7
2016 7
2017 8
2018 4
2019 4
2020 6
2021 5
2022 5
2023 6
2024 6

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98 results

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Page 1
Pathological mitophagy disrupts mitochondrial homeostasis in Leber's hereditary optic neuropathy.
Danese A, Patergnani S, Maresca A, Peron C, Raimondi A, Caporali L, Marchi S, La Morgia C, Del Dotto V, Zanna C, Iannielli A, Segnali A, Di Meo I, Cavaliere A, Lebiedzinska-Arciszewska M, Wieckowski MR, Martinuzzi A, Moraes-Filho MN, Salomao SR, Berezovsky A, Belfort R Jr, Buser C, Ross-Cisneros FN, Sadun AA, Tacchetti C, Broccoli V, Giorgi C, Tiranti V, Carelli V, Pinton P. Danese A, et al. Among authors: tiranti v. Cell Rep. 2022 Jul 19;40(3):111124. doi: 10.1016/j.celrep.2022.111124. Cell Rep. 2022. PMID: 35858578 Free PMC article.
Ethylmalonic Encephalopathy.
Di Meo I, Lamperti C, Tiranti V. Di Meo I, et al. Among authors: tiranti v. 2017 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2017 Sep 21. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 28933811 Free Books & Documents. Review.
Classification and molecular pathogenesis of NBIA syndromes.
Di Meo I, Tiranti V. Di Meo I, et al. Among authors: tiranti v. Eur J Paediatr Neurol. 2018 Mar;22(2):272-284. doi: 10.1016/j.ejpn.2018.01.008. Epub 2018 Jan 17. Eur J Paediatr Neurol. 2018. PMID: 29409688 Review.
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: tiranti v. 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.
Fetal and obstetrics manifestations of mitochondrial diseases.
Alessia A, Anastasia G, Alessia DD, Simona B, Alessandro P, Emanuela B, Valentina B, Valeria T, Nicola P, Dario B. Alessia A, et al. Among authors: valeria t. J Transl Med. 2024 Sep 23;22(1):853. doi: 10.1186/s12967-024-05633-6. J Transl Med. 2024. PMID: 39313811 Free PMC article. Review.
Depletion of mtDNA: syndromes and genes.
Alberio S, Mineri R, Tiranti V, Zeviani M. Alberio S, et al. Among authors: tiranti v. Mitochondrion. 2007 Feb-Apr;7(1-2):6-12. doi: 10.1016/j.mito.2006.11.010. Epub 2006 Dec 5. Mitochondrion. 2007. PMID: 17280874 Review.
98 results