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Lack of association between nuclear factor erythroid-derived 2-like 2 promoter gene polymorphisms and oxidative stress biomarkers in amyotrophic lateral sclerosis patients.
LoGerfo A, Chico L, Borgia L, Petrozzi L, Rocchi A, D'Amelio A, Carlesi C, Caldarazzo Ienco E, Mancuso M, Siciliano G. LoGerfo A, et al. Among authors: chico l. Oxid Med Cell Longev. 2014;2014:432626. doi: 10.1155/2014/432626. Epub 2014 Feb 9. Oxid Med Cell Longev. 2014. PMID: 24672634 Free PMC article.
Hereditary spastic paraparesis in adults. A clinical and genetic perspective from Tuscany.
Orsucci D, Petrucci L, Ienco EC, Chico L, Simi P, Fogli A, Baldinotti F, Simoncini C, LoGerfo A, Carlesi C, Arnoldi A, Bassi MT, Siciliano G, Bonuccelli U, Mancuso M. Orsucci D, et al. Among authors: chico l. Clin Neurol Neurosurg. 2014 May;120:14-9. doi: 10.1016/j.clineuro.2014.02.002. Epub 2014 Feb 17. Clin Neurol Neurosurg. 2014. PMID: 24731568
Methylation analysis of DNA repair genes in Alzheimer's disease.
Coppedè F, Tannorella P, Stoccoro A, Chico L, Siciliano G, Bonuccelli U, Migliore L. Coppedè F, et al. Among authors: chico l. Mech Ageing Dev. 2017 Jan;161(Pt A):105-111. doi: 10.1016/j.mad.2016.04.003. Epub 2016 Apr 11. Mech Ageing Dev. 2017. PMID: 27080585 Clinical Trial.
Mitochondrial DNA haplogroups may influence Fabry disease phenotype.
Simoncini C, Chico L, Concolino D, Sestito S, Fancellu L, Boadu W, Sechi GP, Feliciani C, Gnarra M, Zampetti A, Salviati A, Scarpelli M, Orsucci D, Bonuccelli U, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: chico l. Neurosci Lett. 2016 Aug 26;629:58-61. doi: 10.1016/j.neulet.2016.06.051. Epub 2016 Jun 27. Neurosci Lett. 2016. PMID: 27365132
74 results