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

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

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74 results

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Page 1
Novel cell lines derived from adult human ventricular cardiomyocytes.
Davidson MM, Nesti C, Palenzuela L, Walker WF, Hernandez E, Protas L, Hirano M, Isaac ND. Davidson MM, et al. Among authors: nesti c. J Mol Cell Cardiol. 2005 Jul;39(1):133-47. doi: 10.1016/j.yjmcc.2005.03.003. J Mol Cell Cardiol. 2005. PMID: 15913645
Syndromes associated with mitochondrial DNA depletion.
Nogueira C, Almeida LS, Nesti C, Pezzini I, Videira A, Vilarinho L, Santorelli FM. Nogueira C, et al. Among authors: nesti c. Ital J Pediatr. 2014 Apr 3;40:34. doi: 10.1186/1824-7288-40-34. Ital J Pediatr. 2014. PMID: 24708634 Free PMC article. Review.
Relapsing-Remitting Course of Cystic Leukoencephalopathy.
Rubegni A, Ferrari AR, Pasquariello R, Canapicchi R, Santorelli FM, Nesti C. Rubegni A, et al. Among authors: nesti c. Pediatr Neurol. 2018 Dec;89:63-65. doi: 10.1016/j.pediatrneurol.2018.08.021. Epub 2018 Aug 24. Pediatr Neurol. 2018. PMID: 30340907 No abstract available.
Clinical, Genetic, and Histological Characterization of Patients with Rare Neuromuscular and Mitochondrial Diseases Presenting with Different Cardiomyopathy Phenotypes.
Monda E, Lioncino M, Caiazza M, Simonelli V, Nesti C, Rubino M, Perna A, Mauriello A, Budillon A, Pota V, Bruno G, Varone A, Nigro V, Santorelli FM, Pacileo G, Russo MG, Frisso G, Sampaolo S, Limongelli G. Monda E, et al. Among authors: nesti c. Int J Mol Sci. 2023 May 22;24(10):9108. doi: 10.3390/ijms24109108. Int J Mol Sci. 2023. PMID: 37240454 Free PMC article.
The features of the m.10197G>A mtDNA mutation.
Severino M, Nesti C, Rubegni A, Tolomeo D, Santorelli FM. Severino M, et al. Among authors: nesti c. J Neurol Sci. 2019 May 15;400:184-185. doi: 10.1016/j.jns.2019.04.005. Epub 2019 Apr 4. J Neurol Sci. 2019. PMID: 30978516 No abstract available.
Bi-allelic variants in MDH2: Expanding the clinical phenotype.
Ticci C, Nesti C, Rubegni A, Doccini S, Baldacci J, Dal Canto F, Ragni L, Cordelli DM, Donati MA, Santorelli FM. Ticci C, et al. Among authors: nesti c. Clin Genet. 2022 Feb;101(2):260-264. doi: 10.1111/cge.14088. Epub 2021 Nov 22. Clin Genet. 2022. PMID: 34766628
A Child With Ichthyosis and Liver Failure.
Indolfi G, Iascone M, Remaschi G, Donati MA, Nesti C, Rubegni A, Pezzoli L, Buccoliero AM, Santorelli FM, Resti M. Indolfi G, et al. Among authors: nesti c. J Pediatr Gastroenterol Nutr. 2017 Sep;65(3):e70-e73. doi: 10.1097/MPG.0000000000001645. J Pediatr Gastroenterol Nutr. 2017. PMID: 28562522 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.
74 results