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Results by year

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

Year Number of Results
1975 1
1994 3
1995 1
1996 2
1997 1
1998 3
1999 2
2000 1
2001 4
2002 4
2003 2
2004 4
2005 1
2007 6
2008 2
2009 6
2010 4
2011 3
2012 4
2013 7
2014 7
2015 4
2016 3
2017 8
2018 5
2019 8
2020 6
2021 7
2022 2
2023 4
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Publication date

Search Results

103 results
Results by year
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Page 1
Treatment for gastrointestinal and pancreatic neuroendocrine tumours: a network meta-analysis.
Walter MA, Nesti C, Spanjol M, Kollár A, Bütikofer L, Gloy VL, Dumont RA, Seiler CA, Christ ER, Radojewski P, Briel M, Kaderli RM. Walter MA, et al. Among authors: nesti c. Cochrane Database Syst Rev. 2021 Nov 25;11(11):CD013700. doi: 10.1002/14651858.CD013700.pub2. Cochrane Database Syst Rev. 2021. PMID: 34822169 Free PMC article. Review.
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.
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
Myoclonus in mitochondrial disorders.
Mancuso M, Orsucci D, Angelini C, Bertini E, Catteruccia M, Pegoraro E, Carelli V, Valentino ML, Comi GP, Minetti C, Bruno C, Moggio M, Ienco EC, Mongini T, Vercelli L, Primiano G, Servidei S, Tonin P, Scarpelli M, Toscano A, Musumeci O, Moroni I, Uziel G, Santorelli FM, Nesti C, Filosto M, Lamperti C, Zeviani M, Siciliano G. Mancuso M, et al. Among authors: nesti c. Mov Disord. 2014 May;29(6):722-8. doi: 10.1002/mds.25839. Epub 2014 Feb 7. Mov Disord. 2014. PMID: 24510442
Long term follow-up in two siblings with Sengers syndrome: Case report.
Panicucci C, Schiaffino MC, Nesti C, Derchi M, Trocchio G, Severino M, Stagnaro N, Priolo E, Zara F, Santorelli FM, Bruno C. Panicucci C, et al. Among authors: nesti c. Ital J Pediatr. 2022 Oct 17;48(1):180. doi: 10.1186/s13052-022-01370-y. Ital J Pediatr. 2022. PMID: 36253788 Free PMC article.
Learning from massive testing of mitochondrial disorders: UPD explaining unorthodox transmission.
Tolomeo D, Rubegni A, Nesti C, Barghigiani M, Battini R, D'Amore F, Doccini S, Donati MA, Galatolo D, Giglio S, Guarducci S, Pantaleo M, Pasquariello R, Procopio E, Pochiero F, Tessa A, Santorelli FMM. Tolomeo D, et al. Among authors: nesti c. J Med Genet. 2021 Aug;58(8):543-546. doi: 10.1136/jmedgenet-2020-107644. Epub 2021 Jun 16. J Med Genet. 2021. PMID: 34135091 No abstract available.
103 results