Výsledky vyhledávání - "Massimo Morini"

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers

Publikováno v: JAMA Cardiol
JAMA cardiology, 7(5), 504-512. American Medical Association
JAMA Cardiology, 7(5), 504-512. AMER MEDICAL ASSOC
Mazzanti, A, Kukavica, D, Trancuccio, A, Memmi, M, Bloise, R, Gambelli, P, Marino, M, Ortíz-Genga, M, Morini, M, Monteforte, N, Giordano, U, Keegan, R, Tomasi, L, Anastasakis, A, Davis, A M, Shimizu, W, Blom, N A, Santiago, D J, Napolitano, C, Monserrat, L & Priori, S G 2022, ' Outcomes of Patients with Catecholaminergic Polymorphic Ventricular Tachycardia Treated with β-Blockers ', JAMA cardiology, vol. 7, no. 5, pp. 504-512 . https://doi.org/10.1001/jamacardio.2022.0219

Patients with catecholaminergic polymorphic ventricular tachycardia (CPVT) may experience life-threatening arrhythmic events (LTAEs) despite β-blocker treatment. Further complicating management, the role of implantable cardioverter defibrillator (IC

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c929e7cc08bf8cf5e5f9c580b72e5d54
https://europepmc.org/articles/PMC8968697/

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Decentralized Financial Market Infrastructures: Evolution from Intermediated Structures to Decentralized Structures for Financial Agreements

Autor: Diana Barrero Zalles, Rhomaios Ram, Robert Sams, Daniel Heller, Sara Feenan, Alexander Lipton, Massimo Morini, Tim Swanson, Stanley Yong

Publikováno v: The Journal of FinTech.

Financial market infrastructures (FMIs) have evolved as core elements of highly intermediated financial markets partly due to the technological limitations of the time when they were first designed. Organizations and firms were unable to share record

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c4a23c8c5c859f06b56970a23f146127
https://doi.org/10.1142/s2705109921500024

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Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing

Autor: Valeria Novelli, Mirella Memmi, Alberto Malovini, Andrea Mazzanti, Nian Liu, Ruan Yanfei, Rossana Bongianino, Marco Denegri, Nicola Monteforte, Raffaella Bloise, Massimo Morini, Carlo Napolitano

Publikováno v: Heart rhythm. 19(5)

Evidence for the role of the CACNA1C gene, which encodes for the α-subunit of the cardiac L-type calcium channel CaV1.2, as a cause of the BrS3 variant of Brugada syndrome (BrS) is contradictory.The purpose of this study was to define in a large BrS

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f3b790f35d83efe5dcb88e14a7f6272
https://pubmed.ncbi.nlm.nih.gov/34999275

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Arrhythmogenic Right Ventricular Cardiomyopathy

Autor: Alessandro Faragli, Nicola Monteforte, Raffaella Bloise, Vincenzo Bagnardi, Carlo Napolitano, Nicoletta Orphanou, Riccardo Bellazzi, Kevin Ng, Massimo Morini, Guido Moro, Valeria Novelli, Oronzo Catalano, Patrick Gambelli, Silvia G. Priori, Riccardo Maragna, Valentina Tibollo, Elena Chiodaroli, Mirella Memmi, Andrea Mazzanti

Publikováno v: Journal of the American College of Cardiology. 68:2540-2550

Background Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a leading cause of sudden cardiac death, but its progression over time and predictors of arrhythmias are still being defined. Objectives This study sought to describe the clinical c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::02fe8a30d19be918a08985e188f38b43
https://doi.org/10.1016/j.jacc.2016.09.951

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Efficacy and Limitations of Quinidine in Patients With Brugada Syndrome

Autor: Andrea Mazzanti, Riccardo Bellazzi, Eleonora Pagan, Cristina Raimondo, Massimo Morini, Elisavietta Tenuta, Alice Maltret, Nicola Monteforte, Raffaella Bloise, Mirella Memmi, Barbara Colombi, Maira Marino, Vincenzo Bagnardi, Carlo Napolitano, Antonio Curcio, Samuele Frassoni, Valentina Tibollo, Silvia G. Priori

Publikováno v: Circulation: Arrhythmia and Electrophysiology. 12

Background:Quinidine at high dose is suggested as antiarrhythmic treatment in patients with Brugada Syndrome (BrS), but its efficacy to prevent life-threatening arrhythmic events (LAE) in this population is unproven and its use limited by frequent si

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbed3be9ba848bb035fa09cf59cc90c0
https://doi.org/10.1161/circep.118.007143

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Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome

Autor: Nicola Monteforte, Mirella Memmi, Raffaella Bloise, Alberto Malovini, Carlo Napolitano, Vincenzo Bagnardi, L. Braghieri, Silvia G. Priori, Massimo Morini, Gaetano Vacanti, Eleonora Pagan, Andrea Mazzanti, Patrick Gambelli, Luciana Sacilotto, Lorenzo Monserrat, Martín Ortiz, Riccardo Maragna, Maira Marino, Riccardo Bellazzi

Publikováno v: Repisalud
Instituto de Salud Carlos III (ISCIII)

Long QT syndrome (LQTS) is a common inheritable arrhythmogenic disorder, often secondary to mutations in the KCNQ1, KCNH2, and SCN5A genes. The disease is characterized by a prolonged ventricular repolarization (QTc interval) that confers susceptibil

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b28bd4659aba818714a6ea4925529396
https://hdl.handle.net/20.500.12105/10498

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