Challenges in Molecular Diagnostics of Channelopathies in the Next-Generation Sequencing Era: Less Is More?

Por Novelli, Valeria, Gambelli, Patrick, Memmi, Mirella, Napolitano, Carlo
Publicado no Front Cardiovasc Med (2016)

Clinical utility gene card for: Catecholaminergic polymorphic ventricular tachycardia (CPVT)

Por Napolitano, Carlo, Bloise, Raffaella, Memmi, Mirella, Priori, Silvia Giuliana
Publicado em 2014

Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation

Por Grant, Augustus O., Carboni, Michael P., Neplioueva, Valentina, Starmer, C. Frank, Memmi, Mirella, Napolitano, Carlo, Priori, Silvia
Publicado em 2002

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

Por Mazzanti, Andrea, Maragna, Riccardo, Faragli, Alessandro, Monteforte, Nicola, Bloise, Raffaella, Memmi, Mirella, Novelli, Valeria, Baiardi, Paola, Bagnardi, Vincenzo, Etheridge, Susan P., Napolitano, Carlo, Priori, Silvia G.
Publicado no J Am Coll Cardiol (2016)

Novel Insight Into the Natural History of Short QT Syndrome

Por Mazzanti, Andrea, Kanthan, Ajita, Monteforte, Nicola, Memmi, Mirella, Bloise, Raffaella, Novelli, Valeria, Miceli, Carlotta, O'Rourke, Sean, Borio, Gianluca, Zienciuk-Krajka, Agnieszka, Curcio, Antonio, Surducan, Andreea Elena, Colombo, Mario, Napolitano, Carlo, Priori, Silvia G.
Publicado em 2014