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MODY type 2 P59S GCK mutant: founder effect in South of Italy.
Delvecchio M, Ludovico O, Bellacchio E, Stallone R, Palladino T, Mastroianno S, Zelante L, Sacco M, Trischitta V, Carella M. Delvecchio M, et al. Among authors: mastroianno s. Clin Genet. 2013 Jan;83(1):83-7. doi: 10.1111/j.1399-0004.2012.01856.x. Epub 2012 Mar 26. Clin Genet. 2013. PMID: 22335469
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. Among authors: mastroianno s. 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: mastroianno s, mastroianno m. 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: mastroianno s. 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
31 results