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

Year Number of Results
2002 3
2003 4
2004 1
2005 2
2006 5
2007 5
2008 4
2009 5
2010 5
2011 8
2012 12
2013 6
2014 5
2015 6
2016 9
2017 3
2018 3
2019 3
2020 8
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87 results
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Page 1
Systemic activation of Nrf2 pathway in Parkinson's disease.
Petrillo S, Schirinzi T, Di Lazzaro G, D'Amico J, Colona VL, Bertini E, Pierantozzi M, Mari L, Mercuri NB, Piemonte F, Pisani A. Petrillo S, et al. Among authors: piemonte f. Mov Disord. 2020 Jan;35(1):180-184. doi: 10.1002/mds.27878. Epub 2019 Nov 4. Mov Disord. 2020. PMID: 31682033
Targeting NRF2 for the Treatment of Friedreich's Ataxia: A Comparison among Drugs.
Petrillo S, D'Amico J, La Rosa P, Bertini ES, Piemonte F. Petrillo S, et al. Among authors: piemonte f. Int J Mol Sci. 2019 Oct 21;20(20):5211. doi: 10.3390/ijms20205211. Int J Mol Sci. 2019. PMID: 31640150 Free PMC article.
Nrf2-Inducers Counteract Neurodegeneration in Frataxin-Silenced Motor Neurons: Disclosing New Therapeutic Targets for Friedreich's Ataxia.
Petrillo S, Piermarini E, Pastore A, Vasco G, Schirinzi T, Carrozzo R, Bertini E, Piemonte F. Petrillo S, et al. Among authors: piemonte f. Int J Mol Sci. 2017 Oct 18;18(10):2173. doi: 10.3390/ijms18102173. Int J Mol Sci. 2017. PMID: 29057804 Free PMC article.
Oxidative stress in Duchenne muscular dystrophy: focus on the NRF2 redox pathway.
Petrillo S, Pelosi L, Piemonte F, Travaglini L, Forcina L, Catteruccia M, Petrini S, Verardo M, D'Amico A, Musarò A, Bertini E. Petrillo S, et al. Among authors: piemonte f. Hum Mol Genet. 2017 Jul 15;26(14):2781-2790. doi: 10.1093/hmg/ddx173. Hum Mol Genet. 2017. PMID: 28472288
The cytoskeletal arrangements necessary to neurogenesis.
Compagnucci C, Piemonte F, Sferra A, Piermarini E, Bertini E. Compagnucci C, et al. Among authors: piemonte f. Oncotarget. 2016 Apr 12;7(15):19414-29. doi: 10.18632/oncotarget.6838. Oncotarget. 2016. PMID: 26760504 Free PMC article. Review.
Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy.
Flex E, Niceta M, Cecchetti S, Thiffault I, Au MG, Capuano A, Piermarini E, Ivanova AA, Francis JW, Chillemi G, Chandramouli B, Carpentieri G, Haaxma CA, Ciolfi A, Pizzi S, Douglas GV, Levine K, Sferra A, Dentici ML, Pfundt RR, Le Pichon JB, Farrow E, Baas F, Piemonte F, Dallapiccola B, Graham JM Jr, Saunders CJ, Bertini E, Kahn RA, Koolen DA, Tartaglia M. Flex E, et al. Among authors: piemonte f. Am J Hum Genet. 2016 Oct 6;99(4):962-973. doi: 10.1016/j.ajhg.2016.08.003. Epub 2016 Sep 22. Am J Hum Genet. 2016. PMID: 27666370 Free PMC article.
Nrf2 Induction Re-establishes a Proper Neuronal Differentiation Program in Friedreich's Ataxia Neural Stem Cells.
La Rosa P, Russo M, D'Amico J, Petrillo S, Aquilano K, Lettieri-Barbato D, Turchi R, Bertini ES, Piemonte F. La Rosa P, et al. Among authors: piemonte f. Front Cell Neurosci. 2019 Jul 31;13:356. doi: 10.3389/fncel.2019.00356. eCollection 2019. Front Cell Neurosci. 2019. PMID: 31417369 Free PMC article.
Serum uric acid in Friedreich Ataxia.
Schirinzi T, Vasco G, Zanni G, Petrillo S, Piemonte F, Castelli E, Bertini ES. Schirinzi T, et al. Among authors: piemonte f. Clin Biochem. 2018 Apr;54:139-141. doi: 10.1016/j.clinbiochem.2018.01.022. Epub 2018 Feb 2. Clin Biochem. 2018. PMID: 29409831
Infantile mitochondrial disorders.
Carrozzo R, Piemonte F, Tessa A, Lucioli S, Rizza T, Meschini MC, Fattori F, Santorelli FM. Carrozzo R, et al. Among authors: piemonte f. Biosci Rep. 2007 Jun;27(1-3):105-12. doi: 10.1007/s10540-007-9039-y. Biosci Rep. 2007. PMID: 17486440 Free article. Review.
ISCA1 mutation in a patient with infantile-onset leukodystrophy causes defects in mitochondrial [4Fe-4S] proteins.
Torraco A, Stehling O, Stümpfig C, Rösser R, De Rasmo D, Fiermonte G, Verrigni D, Rizza T, Vozza A, Di Nottia M, Diodato D, Martinelli D, Piemonte F, Dionisi-Vici C, Bertini E, Lill R, Carrozzo R. Torraco A, et al. Among authors: piemonte f. Hum Mol Genet. 2018 Oct 15;27(20):3650. doi: 10.1093/hmg/ddy273. Hum Mol Genet. 2018. PMID: 30113620 No abstract available.
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