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Page 1
Oxidative stress biomarkers in Fabry disease: is there a room for them?
Simoncini C, Torri S, Montano V, Chico L, Gruosso F, Tuttolomondo A, Pinto A, Simonetta I, Cianci V, Salviati A, Vicenzi V, Marchi G, Girelli D, Concolino D, Sestito S, Zedde M, Siciliano G, Mancuso M. Simoncini C, et al. Among authors: vicenzi v. J Neurol. 2020 Dec;267(12):3741-3752. doi: 10.1007/s00415-020-10044-w. Epub 2020 Jul 27. J Neurol. 2020. PMID: 32719972 Free PMC article.
Changing therapeutic strategies and persistence to disease-modifying treatments in a population of multiple sclerosis patients from Veneto region, Italy.
Marangi A, Farina G, Vicenzi V, Forlivesi S, Calabria F, Marchioretto F, Forgione A, Rossi F, Stenta G, Vianello M, Gajofatto A, Benedetti MD. Marangi A, et al. Among authors: vicenzi v. Mult Scler Relat Disord. 2020 Jun;41:102004. doi: 10.1016/j.msard.2020.102004. Epub 2020 Feb 10. Mult Scler Relat Disord. 2020. PMID: 32078935
Prevalence, characteristics, and survival of children with esophageal atresia: A 32-year population-based study including 1,417,724 consecutive newborns.
Cassina M, Ruol M, Pertile R, Midrio P, Piffer S, Vicenzi V, Saugo M, Stocco CF, Gamba P, Clementi M. Cassina M, et al. Among authors: vicenzi v. Birth Defects Res A Clin Mol Teratol. 2016 Jul;106(7):542-8. doi: 10.1002/bdra.23493. Epub 2016 Mar 2. Birth Defects Res A Clin Mol Teratol. 2016. PMID: 26931365
FBXO28 is a critical gene of the 1q41q42 microdeletion syndrome.
Cassina M, Rigon C, Casarin A, Vicenzi V, Salviati L, Clementi M. Cassina M, et al. Among authors: vicenzi v. Am J Med Genet A. 2015 Jun;167(6):1418-20. doi: 10.1002/ajmg.a.37033. Epub 2015 Apr 21. Am J Med Genet A. 2015. PMID: 25900767 No abstract available.