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An "inflammatory" mitochondrial myopathy. A case report.
Mancuso M, Orsucci D, Ienco EC, Ricci G, Ali G, Servadio A, Fontanini G, Filosto M, Vielmi V, Rocchi A, Petrozzi L, Logerfo A, Siciliano G. Mancuso M, et al. Neuromuscul Disord. 2013 Nov;23(11):907-10. doi: 10.1016/j.nmd.2013.07.011. Epub 2013 Aug 8. Neuromuscul Disord. 2013. PMID: 24011700
Mitochondrial stroke-like episodes: The search for new therapies.
Orsucci D, Caldarazzo Ienco E, Montano V, Siciliano G, Mancuso M. Orsucci D, et al. Among authors: mancuso m. Pharmacol Res. 2022 Jun;180:106228. doi: 10.1016/j.phrs.2022.106228. Epub 2022 Apr 21. Pharmacol Res. 2022. PMID: 35462010
A new truncating MPZ mutation associated with a very mild CMT1 B phenotype.
Piazza S, Baldinotti F, Fogli A, Conidi ME, Michelucci A, Ienco EC, Mancuso M, Simi P, Siciliano G. Piazza S, et al. Among authors: mancuso m. Neuromuscul Disord. 2010 Dec;20(12):817-9. doi: 10.1016/j.nmd.2010.08.003. Epub 2010 Sep 17. Neuromuscul Disord. 2010. PMID: 20850974
Revealing the Complexity of Mitochondrial DNA-Related Disorders.
Orsucci D, Siciliano G, Mancuso M. Orsucci D, et al. Among authors: mancuso m. EBioMedicine. 2018 Apr;30:3-4. doi: 10.1016/j.ebiom.2018.03.007. Epub 2018 Mar 9. EBioMedicine. 2018. PMID: 29550239 Free PMC article. No abstract available.
Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions.
Formichi P, Cardone N, Taglia I, Cardaioli E, Salvatore S, Gerfo AL, Simoncini C, Montano V, Siciliano G, Mancuso M, Malandrini A, Federico A, Dotti MT. Formichi P, et al. Among authors: mancuso m. Neurol Sci. 2020 Dec;41(12):3653-3662. doi: 10.1007/s10072-020-04422-5. Epub 2020 Jun 6. Neurol Sci. 2020. PMID: 32504279
1,026 results