Zobrazeno 1 - 10 of 17 pro vyhledávání: '"Maira Marino"'
1
Value of 3D echocardiography in the diagnosis of arrhythmogenic right ventricular cardiomyopathy
Autor: Karima Addetia, Andrea Mazzanti, Riccardo Maragna, Lorenzo Monti, Megan Yamat, Deni Kukavica, Eleonora Pagan, Kanako Kishiki, Aldo Prado, Maira Marino, Vincenzo Bagnardi, Silvia Priori, Roberto M Lang
Aims The 2010 Task Force Criteria (TFC) require that both right ventricular (RV) regional wall-motion abnormalities (WMA) and specific RV size cut-offs be met in order to fulfil one of the major criterion for arrhythmogenic right ventricular cardiomy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87643d22c5f8f6dc18777e00078f9e9b
http://hdl.handle.net/10281/392117
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2
Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia Treated With β-Blockers
Autor: Andrea Mazzanti, Deni Kukavica, Alessandro Trancuccio, Mirella Memmi, Raffaella Bloise, Patrick Gambelli, Maira Marino, Martín Ortíz-Genga, Massimo Morini, Nicola Monteforte, Umberto Giordano, Roberto Keegan, Luca Tomasi, Aristides Anastasakis, Andrew M. Davis, Wataru Shimizu, Nico A. Blom, Demetrio Julián Santiago, Carlo Napolitano, Lorenzo Monserrat, Silvia G. Priori
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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3
764 Prevalence and clinical implications of cardiac involvement in individuals with paucisymptomatic SARS-CoV-2 infection
Autor: Alessandro Trancuccio, Andrea Mazzanti, Deni Kukavica, Carlo Arnò, Matteo Sturla, Maira Marino, Raffaela Bloise, Carlo Napolitano, Lorenzo Monti, Silvia G. Priori
Publikováno v: European Heart Journal Supplements : Journal of the European Society of Cardiology
Aims Myocardial involvement has been reported in SARS-CoV-2 infection, especially in hospitalized patients during the acute phase of the disease. However, the exact prevalence and the clinical implications of cardiac involvement in young individuals
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::657b381a27b0e9fb24fa18d6fb7709bb
http://europepmc.org/articles/PMC8689754
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5
Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Autor: Eyal Nof, Fernando E.S. Cruz, Victor Expósito-García, Luciana Sacilotto, Andrea Mazzanti, Jessica Sánchez-Quiñones, Elżbieta Katarzyna Biernacka, Esther Zorio, Deni Kukavica, Carmen Muñoz-Esparza, Julio Hernandez-Afonso, Elisa Tavazzani, Oscar Campuzano, Asaf Danon, Juan Jiménez-Jáimez, Martín Ortiz, Tekla Chargeishvili, Lorenzo Monserrat, Agnieszka Zienciuk-Krajka, Aristides Anastasakis, Carlo Napolitano, Eleonora Pagan, Maira Marino, Dmitri Guz, Amaya Garcia-Fernandez, Mirella Memmi, Beata Średniawa, Natália Olivetti, Valeria A. Sansone, Rumen Marinov, Georgia Sarquella-Brugada, Maite Izquierdo, Nicola Monteforte, Raffaella Bloise, María Eugenia Fuentes, Irena Andršová, Vincenzo Bagnardi, Silvia G. Priori, Alessandro Trancuccio, Anastasia Garoufi
Publikováno v: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
BACKGROUND Andersen-Tawil Syndrome type 1 (ATS1) is a rare arrhythmogenic disorder, caused by loss-of-function mutations in the KCNJ2 gene. We present here the largest cohort of patients with ATS1 with outcome data reported. OBJECTIVES This study sou
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95db8f14bf6650a4244ac62d01a83ee2
https://pubmed.ncbi.nlm.nih.gov/32299590
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6
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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7
Unexpected Risk Profile of a Large Pediatric Population With Brugada Syndrome
Autor: Stefano Mameli, Carlo Napolitano, Cristina Raimondo, Maira Marino, Paz Ovics, Alice Maltret, Ayelet Shauer, Silvia G. Priori, Andrea Mazzanti, Nicola Monteforte, Raffaella Bloise, Vincenzo Bagnardi
Publikováno v: Journal of the American College of Cardiology. 73(14)
The clinical course of Brugada syndrome (BrS) in children and adolescents is incompletely defined due to the rarity of the phenotype in the first decades of life. In 2007, Probst et al. [(1)][1] reported the outcome of 30 pediatric patients with 3 ye
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b460c66d1d30b253709eac1eb9ce9058
https://pubmed.ncbi.nlm.nih.gov/30975305
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8
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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9
Abstract 23071: Hydroquinidine Abolishes Life-threatening Arrhythmic Events in Patients With Short QT Syndrome
Autor: Andrea Mazzanti, Riccardo Maragna, Gaetano Vacanti, Anna Kostopoulou, Maira Marino, Nicola Monteforte, Raffaella Bloise, Eleonora Pagan, Carlo Napolitano, Vincenzo Bagnardi, Silvia G. Priori
Publikováno v: Circulation. 136
Background: Short QT Syndrome (SQTS) is one of the rarest and most lethal inherited arrhythmogenic syndromes. Preliminary data have shown that hydroquinidine (HQ) is effective in prolonging the duration of QT interval and in preventing the induction
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::73755020ab42bff734f5aee4006f6e91
https://doi.org/10.1161/circ.136.suppl_1.23071
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10
Hydroquinidine Prevents Life-Threatening Arrhythmic Events in Patients With Short QT Syndrome
Autor: Silvia G. Priori, Riccardo Bellazzi, Riccardo Maragna, Gaetano Vacanti, Andrea Mazzanti, Valentina Tibollo, Katherine Underwood, Carlo Napolitano, Maira Marino, Anna Kostopoulou, Nicola Monteforte, Eleonora Pagan, Raffaella Bloise, Vincenzo Bagnardi
Publikováno v: Repisalud
Instituto de Salud Carlos III (ISCIII)
Short QT syndrome (SQTS) is a rare and life-threatening arrhythmogenic syndrome characterized by abbreviated repolarization. Hydroquinidine (HQ) prolongs the QT interval in SQTS patients, although whether it reduces cardiac events is currently unknow
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b05c22bc634680660a03d9f0622550
http://hdl.handle.net/20.500.12105/10497
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