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Combined Clinical, Molecular, and Muscle Biopsy Approach to Unveil Prevalence and Clinical Features of Rare Neuromuscular and Mitochondrial Diseases in Patients With Cardiomyopathies.
Lioncino M, Monda E, Caiazza M, Simonelli V, Nesti C, Mauriello A, Budillon A, Di Santo A, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Lioncino M, et al. Among authors: nesti c. Circ Genom Precis Med. 2023 Aug;16(4):412-414. doi: 10.1161/CIRCGEN.123.004122. Epub 2023 May 17. Circ Genom Precis Med. 2023. PMID: 37194584 No abstract available.
Additive effect of DNAJC30 and NDUFA9 mutations causing Leigh syndrome.
Nesti C, Ticci C, Rubegni A, Doccini S, Scaturro G, Vetro A, Guerrini R, Santorelli FM, Procopio E. Nesti C, et al. J Neurol. 2023 Jun;270(6):3266-3269. doi: 10.1007/s00415-023-11673-7. Epub 2023 Mar 20. J Neurol. 2023. PMID: 36939934 No abstract available.
MERRF syndrome without ragged-red fibers: the need for molecular diagnosis.
Mancuso M, Petrozzi L, Filosto M, Nesti C, Rocchi A, Choub A, Pistolesi S, Massetani R, Fontanini G, Siciliano G. Mancuso M, et al. Among authors: nesti c. Biochem Biophys Res Commun. 2007 Mar 23;354(4):1058-60. doi: 10.1016/j.bbrc.2007.01.099. Epub 2007 Jan 26. Biochem Biophys Res Commun. 2007. PMID: 17275787
The role of mitochondria in stem cell biology.
Nesti C, Pasquali L, Vaglini F, Siciliano G, Murri L. Nesti C, et al. Biosci Rep. 2007 Jun;27(1-3):165-71. doi: 10.1007/s10540-007-9044-1. Biosci Rep. 2007. PMID: 17484045 Review.
113 results