Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

109 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Lack of association between mtDNA haplogroups and Alzheimer's disease in Tuscany.
Mancuso M, Nardini M, Micheli D, Rocchi A, Nesti C, Giglioli NJ, Petrozzi L, Rossi C, Ceravolo R, Bacci A, Choub A, Ricci G, Tognoni G, Manca ML, Siciliano G, Murri L. Mancuso M, et al. Among authors: nesti c. Neurol Sci. 2007 Jun;28(3):142-7. doi: 10.1007/s10072-007-0807-z. Epub 2007 Jun 30. Neurol Sci. 2007. PMID: 17603766
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.
Mitochondrial syndromic sensorineural hearing loss.
Forli F, Passetti S, Mancuso M, Seccia V, Siciliano G, Nesti C, Berrettini S. Forli F, et al. Among authors: nesti c. Biosci Rep. 2007 Jun;27(1-3):113-23. doi: 10.1007/s10540-007-9040-5. Biosci Rep. 2007. PMID: 17487579
Mitochondrial DNA haplogroups do not influence the Huntington's disease phenotype.
Mancuso M, Kiferle L, Petrozzi L, Nesti C, Rocchi A, Ceravolo R, Orsucci D, Maluccio MR, Bonuccelli U, Filosto M, Siciliano G, Murri L. Mancuso M, et al. Among authors: nesti c. Neurosci Lett. 2008 Oct 17;444(1):83-6. doi: 10.1016/j.neulet.2008.08.013. Epub 2008 Aug 8. Neurosci Lett. 2008. PMID: 18706972
109 results