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

Year Number of Results
1957 1
1959 9
1960 7
1961 11
1962 2
1963 2
1964 3
1965 2
1966 6
1967 1
1968 8
1969 8
1971 1
1973 1
1974 2
1977 1
1979 1
1980 1
1981 1
1982 1
1996 1
1999 4
2000 3
2001 5
2002 2
2003 3
2004 3
2005 2
2006 3
2007 1
2008 9
2009 10
2010 3
2011 2
2012 3
2013 1
2014 2
2015 1
2016 3
2017 4
2018 3
2019 6
2020 6
2021 7
2022 2
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Article type
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Search Results

148 results
Results by year
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Page 1
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): Position paper on diagnosis, prognosis, and treatment by the MNGIE International Network.
Hirano M, Carelli V, De Giorgio R, Pironi L, Accarino A, Cenacchi G, D'Alessandro R, Filosto M, Martí R, Nonino F, Pinna AD, Baldin E, Bax BE, Bolletta A, Bolletta R, Boschetti E, Cescon M, D'Angelo R, Dotti MT, Giordano C, Gramegna LL, Levene M, Lodi R, Mandel H, Morelli MC, Musumeci O, Pugliese A, Scarpelli M, Siniscalchi A, Spinazzola A, Tal G, Torres-Torronteras J, Vignatelli L, Zaidman I, Zoller H, Rinaldi R, Zeviani M. Hirano M, et al. Among authors: spinazzola a. J Inherit Metab Dis. 2021 Mar;44(2):376-387. doi: 10.1002/jimd.12300. Epub 2020 Sep 8. J Inherit Metab Dis. 2021. PMID: 32898308 Free PMC article. Review.
Mitochondrial diseases: translation matters.
Pearce S, Nezich CL, Spinazzola A. Pearce S, et al. Among authors: spinazzola a. Mol Cell Neurosci. 2013 Jul;55:1-12. doi: 10.1016/j.mcn.2012.08.013. Epub 2012 Sep 7. Mol Cell Neurosci. 2013. PMID: 22986124 Review.
Beyond the unwinding: role of TOP1MT in mitochondrial translation.
Baechler SA, Dalla Rosa I, Spinazzola A, Pommier Y. Baechler SA, et al. Among authors: spinazzola a. Cell Cycle. 2019 Oct;18(19):2377-2384. doi: 10.1080/15384101.2019.1646563. Epub 2019 Aug 9. Cell Cycle. 2019. PMID: 31345095 Free PMC article. Review.
Mitochondrial disorders.
Zeviani M, Spinazzola A. Zeviani M, et al. Among authors: spinazzola a. Curr Neurol Neurosci Rep. 2003 Sep;3(5):423-32. doi: 10.1007/s11910-003-0026-9. Curr Neurol Neurosci Rep. 2003. PMID: 12914686 Review.
MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy.
Bugiardini E, Mitchell AL, Rosa ID, Horning-Do HT, Pitmann AM, Poole OV, Holton JL, Shah S, Woodward C, Hargreaves I, Quinlivan R, Amunts A, Wiesner RJ, Houlden H, Holt IJ, Hanna MG, Pitceathly RDS, Spinazzola A. Bugiardini E, et al. Among authors: spinazzola a. Hum Mol Genet. 2019 Aug 15;28(16):2711-2719. doi: 10.1093/hmg/ddz093. Hum Mol Genet. 2019. PMID: 31039582 Free PMC article.
Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease.
Horga A, Manole A, Mitchell AL, Bugiardini E, Hargreaves IP, Mowafi W, Bettencourt C, Blakely EL, He L, Polke JM, Woodward CE, Dalla Rosa I, Shah S, Pittman AM, Quinlivan R, Reilly MM, Taylor RW, Holt IJ, Hanna MG, Pitceathly RDS, Spinazzola A, Houlden H. Horga A, et al. Among authors: spinazzola a. Mol Biol Rep. 2021 Mar;48(3):2093-2104. doi: 10.1007/s11033-021-06188-1. Epub 2021 Mar 19. Mol Biol Rep. 2021. PMID: 33742325
Nuclear genes in mitochondrial disorders.
Zeviani M, Spinazzola A, Carelli V. Zeviani M, et al. Among authors: spinazzola a. Curr Opin Genet Dev. 2003 Jun;13(3):262-70. doi: 10.1016/s0959-437x(03)00052-2. Curr Opin Genet Dev. 2003. PMID: 12787788 Review.
148 results