Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Patrick Gambelli"'
Autor:
Oronzo Catalano, Giulia Bendotti, Teresa L. Aloi, Alberto Ferrari Bardile, Mirella Memmi, Patrick Gambelli, Daniela Zanaboni, Alessandra Gualco, Emanuela Cattaneo, Antonio Mazza, Mauro Frascaroli, Esmeralda Eshja, Riccardo Bellazzi, Paolo Poggi, Giovanni Forni, Maria Teresa La Rovere
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 2 (2023)
Background Atherosclerosis vulnerability regression has been evidenced mostly in randomized clinical trials with intensive lipid‐lowering therapy. We aimed to demonstrate vulnerability regression in real life, with a comprehensive quantitative meth
Externí odkaz:
https://doaj.org/article/40f95a60d3784b2ca6dc93ece95aea6d
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
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/
https://europepmc.org/articles/PMC8968697/
Autor:
Raffaella Bloise, Carlo Napolitano, Francesca La Rosa, Patrick Gambelli, Mirella Memmi, Antonio Curcio, Andrea Mazzanti, Alberto Malovini, Riccardo Bellazzi, Ciro Indolfi
Publikováno v:
Heart rhythm. 18(10)
Background The genetic architecture of Brugada syndrome (BrS) is emerging as an increasingly complex area of investigation. The identification of genetically homogeneous populations can provide mechanistic insights and improve genotype-phenotype corr
Autor:
Carlo Napolitano, Giulio G. Stefanini, Pasquale De Cata, Nicola Monteforte, Martina Molteni, Raffaella Bianchini, Patrick Gambelli, Raffaella Bloise, Massimo Morini, Andrea Carbone, Annalisa Carlucci, Silvia Sozzi, Deni Kukavica, Martina Briani, Giacomo Viggiani, Stefano Marelli, Carlo Locatelli, Francesco Cannata, Luca Tomasi, Alessandro Trancuccio, Piero Ceriana, Gianluigi Condorelli, Sara Negri, Rita Salgarello, Silvia G. Priori, Andrea Mazzanti, Francesco Fanfulla, Mirella Memmi, Francesca Bulian, Tommaso Manciulli, Luca Chiovato
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb8a14b26d535ad0a56ab69b559e1f4e
http://hdl.handle.net/11383/2104087
http://hdl.handle.net/11383/2104087
Autor:
Giovanna Nicora, Alberto Malovini, Silvia G. Priori, Patrick Gambelli, Carlo Napolitano, Mirella Memmi, Riccardo Bellazzi, Andrea Mazzanti, Ivan Limongelli
Publikováno v:
Human Mutation. 39:1835-1846
Variant interpretation for the diagnosis of genetic diseases is a complex process. The American College of Medical Genetics and Genomics, with the Association for Molecular Pathology, have proposed a set of evidence-based guidelines to support varian
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
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)
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
https://hdl.handle.net/20.500.12105/10498
Autor:
Andrea, Mazzanti, Kevin, Ng, Alessandro, Faragli, Riccardo, Maragna, Elena, Chiodaroli, Nicoletta, Orphanou, Nicola, Monteforte, Mirella, Memmi, Patrick, Gambelli, Valeria, Novelli, Raffaella, Bloise, Oronzo, Catalano, Guido, Moro, Valentina, Tibollo, Massimo, Morini, Riccardo, Bellazzi, Carlo, Napolitano, Vincenzo, Bagnardi, Silvia G, Priori
Publikováno v:
Journal of the American College of Cardiology. 68(23)
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.This study sought to describe the clinical course of ARVC and occur
Publikováno v:
Frontiers in Cardiovascular Medicine
Inherited arrhythmogenic diseases (IADs – also called cardiac channelopathies) are defined as a group of genetic diseases characterized by electrically unstable substrate in a structurally normal heart (1). Genetic testing in cardiac channelopathie