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Role of the APOE polymorphism in carotid and lower limb revascularization: A prospective study from Southern Italy.
Mastroianno S, Di Stolfo G, Seripa D, Pacilli MA, Paroni G, Coli C, Urbano M, d'Arienzo C, Gravina C, Potenza DR, De Luca G, Greco A, Russo A. Mastroianno S, et al. Among authors: di stolfo g. PLoS One. 2017 Mar 1;12(3):e0171055. doi: 10.1371/journal.pone.0171055. eCollection 2017. PLoS One. 2017. PMID: 28249002 Free PMC article. Clinical Trial.
Sudden cardiac death in J wave syndrome with short QT associated to a novel mutation in Nav 1.8 coding gene SCN10A: First case report for a possible pharmacogenomic role.
Di Stolfo G, Palumbo P, Castellana S, Mastroianno S, Biagini T, Palumbo O, Leone MP, De Luca G, Potenza DR, Mazza T, Russo AA, Carella M. Di Stolfo G, et al. J Electrocardiol. 2018 Sep-Oct;51(5):809-813. doi: 10.1016/j.jelectrocard.2018.06.005. Epub 2018 Jun 9. J Electrocardiol. 2018. PMID: 30177317
Timing of clopidogrel loading dose on peripheral blood endothelial progenitor cells, SDF-1α and neointimal hyperplasia in carotid stenting.
Di Stolfo G, Mastroianno S, Ruggieri M, Fontana A, Marinucci R, Copetti M, Minervini MM, Savino L, Mastroianno M, Savino M, Pacilli MA, Di Mauro L, Potenza DR, Cascavilla N, Paroni G, Russo A. Di Stolfo G, et al. Among authors: di mauro l. Clin Hemorheol Microcirc. 2019;72(1):23-38. doi: 10.3233/CH-180429. Clin Hemorheol Microcirc. 2019. PMID: 30320560 Clinical Trial.
Sudden death in mild hypertrophic cardiomyopathy with compound DSG2/DSC2/MYH6 mutations: Revisiting phenotype after genetic assessment in a master runner athlete.
Castellana S, Mastroianno S, Palumbo P, Palumbo O, Biagini T, Leone MP, De Luca G, Potenza DR, Amico CM, Mazza T, Russo A, Di Stolfo G, Carella M. Castellana S, et al. Among authors: di stolfo g. J Electrocardiol. 2019 Mar-Apr;53:95-99. doi: 10.1016/j.jelectrocard.2019.01.002. Epub 2019 Jan 2. J Electrocardiol. 2019. PMID: 30716529
36 results