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835 results on '"Crotti, Lia"'

1. Therapeutic Efficacy of Mexiletine for Long QT Syndrome Type 2: Evidence From Human Induced Pluripotent Stem Cell–Derived Cardiomyocytes, Transgenic Rabbits, and Patients

Author

Crotti, Lia, Neves, Raquel, Dagradi, Federica, Musu, Giulia, Giannetti, Federica, Bos, J. Martijn, Barbieri, Miriam, Cerea, Paolo, Giovenzana, Fulvio L.F., Torchio, Margherita, Mura, Manuela, Gnecchi, Massimiliano, Conte, Giulio, Auricchio, Angelo, Sala, Luca, Odening, Katja E., Ackerman, Michael J., and Schwartz, Peter J.

Published
2024
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3. ECG/echo indexes in the diagnostic approach to amyloid cardiomyopathy: A head-to-head comparison from the AC-TIVE study

Author

Longo, Francesca, Rossi, Maddalena, Varrà, Guerino Giuseppe, Saro, Riccardo, Dore, Franca, Girardi, Francesca, Vergaro, Giuseppe, Musumeci, Beatrice, Autore, Camillo, Cappelli, Francesco, Perfetto, Federico, Olivotto, Iacopo, Favale, Stefano, Carella, Maria Cristina, Guaricci, Andrea Igoren, Ciccone, Marco Matteo, Di Bella, Gianluca, Tomasoni, Daniela, Rella, Valeria, Branzi, Giovanna, Badano, Luigi, Parati, Gianfranco, Palmiero, Giuseppe, Caiazza, Martina, Caponetti, Angelo Giuseppe, Saturi, Giulia, Labate, Marianna Eleonora, Andreis, Alessandro, Paneva, Elena, De Ferrari, Gaetano Maria, Di Ienno, Luca, De Carli, Giuseppe, Giacomin, Elisa, Arzilli, Chiara, Pagura, Linda, Porcari, Aldostefano, Cameli, Matteo, Biagini, Elena, Canepa, Marco, Crotti, Lia, Imazio, Massimo, Forleo, Cinzia, Pavasini, Rita, Limongelli, Giuseppe, Perlini, Stefano, Metra, Marco, Boriani, Giuseppe, Emdin, Michele, Sinagra, Gianfranco, and Merlo, Marco

Published
2024
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4. Clinical Management of Brugada Syndrome: Commentary From the Experts

Author

Cutler, Michael J., Eckhardt, Lee L., Kaufman, Elizabeth S., Arbelo, Elena, Behr, Elijah R., Brugada, Pedro, Cerrone, Marina, Crotti, Lia, deAsmundis, Carlo, Gollob, Michael H., Horie, Minoru, Huang, David T., Krahn, Andrew D., London, Barry, Lubitz, Steven A., Mackall, Judith A., Nademanee, Koonlawee, Perez, Marco V., Probst, Vincent, Roden, Dan M., Sacher, Frederic, Sarquella-Brugada, Georgia, Scheinman, Melvin M., Shimizu, Wataru, Shoemaker, Benjamin, Sy, Raymond W., Watanabe, Atsuyuki, and Wilde, Arthur A.M.

Published
2024
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5. Worldwide Survey of COVID-19–Associated Arrhythmias

Author

Coromilas, Ellie J, Kochav, Stephanie, Goldenthal, Isaac, Biviano, Angelo, Garan, Hasan, Goldbarg, Seth, Kim, Joon-Hyuk, Yeo, Ilhwan, Tracy, Cynthia, Ayanian, Shant, Akar, Joseph, Singh, Avinainder, Jain, Shashank, Zimerman, Leandro, Pimentel, Maurício, Osswald, Stefan, Twerenbold, Raphael, Schaerli, Nicolas, Crotti, Lia, Fabbri, Daniele, Parati, Gianfranco, Li, Yi, Atienza, Felipe, Zatarain, Eduardo, Tse, Gary, Leung, Keith Sai Kit, Guevara-Valdivia, Milton E, Rivera-Santiago, Carlos A, Soejima, Kyoko, De Filippo, Paolo, Ferrari, Paola, Malanchini, Giovanni, Kanagaratnam, Prapa, Khawaja, Saud, Mikhail, Ghada W, Scanavacca, Mauricio, Hajjar, Ludhmila Abrahão, Rizerio, Brenno, Sacilotto, Luciana, Mollazadeh, Reza, Eslami, Masoud, far, Vahideh Laleh, Mattioli, Anna Vittoria, Boriani, Giuseppe, Migliore, Federico, Cipriani, Alberto, Donato, Filippo, Compagnucci, Paolo, Casella, Michela, Dello Russo, Antonio, Coromilas, James, Aboyme, Andrew, O’Brien, Connor Galen, Rodriguez, Fatima, Wang, Paul J, Naniwadekar, Aditi, Moey, Melissa, Kow, Chia Siang, Cheah, Wee Kooi, Auricchio, Angelo, Conte, Giulio, Hwang, Jongmin, Han, Seongwook, Lazzerini, Pietro Enea, Franchi, Federico, Santoro, Amato, Capecchi, Pier Leopoldo, Joglar, Jose A, Rosenblatt, Anna G, Zardini, Marco, Bricoli, Serena, Bonura, Rosario, Echarte-Morales, Julio, Benito-González, Tomás, Minguito-Carazo, Carlos, Fernández-Vázquez, Felipe, and Wan, Elaine Y

Subjects
Biomedical and Clinical Sciences, Medical Physiology, Cardiovascular Medicine and Haematology, Clinical Sciences, Aged, Arrhythmias, Cardiac, COVID-19, Cardiac Electrophysiology, Comorbidity, Electrophysiologic Techniques, Cardiac, Female, Global Health, Health Care Surveys, Healthcare Disparities, Humans, Incidence, Male, Middle Aged, Practice Patterns, Physicians', Prevalence, Prognosis, Retrospective Studies, Risk Assessment, Time Factors, arrhythmia, atrial fibrillation, atrial flutter, bradycardia, tachycardia, torsade de pointes, Cardiorespiratory Medicine and Haematology, Cardiovascular System & Hematology, Cardiovascular medicine and haematology, Clinical sciences, Medical physiology
Abstract

[Figure: see text].

Published
2021

6. The Lancet Commission to reduce the global burden of sudden cardiac death: a call for multidisciplinary action

Author

Marijon, Eloi, Narayanan, Kumar, Smith, Karen, Barra, Sérgio, Basso, Cristina, Blom, Marieke T, Crotti, Lia, D'Avila, Andre, Deo, Rajat, Dumas, Florence, Dzudie, Anastase, Farrugia, Audrey, Greeley, Kaitlyn, Hindricks, Gerhard, Hua, Wei, Ingles, Jodie, Iwami, Taku, Junttila, Juhani, Koster, Rudolph W, Le Polain De Waroux, Jean-Benoît, Olasveengen, Theresa M, Ong, Marcus E H, Papadakis, Michael, Sasson, Comilla, Shin, Sang Do, Tse, Hung-Fat, Tseng, Zian, Van Der Werf, Christian, Folke, Fredrik, Albert, Christine M, and Winkel, Bo Gregers

Published
2023
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7. Abstract 16660: Precision Diagnosis of Hypertrophic Cardiomyopathy: A New Definition of Inappropriate Hypertrophy

Author

Shiwani, Hunain, Davies, Rhodri, Topriceanu, Constantin-Cristian, Owens, Anjali T, Raman, Betty, Ditaranto, Raffaello, Augusto, Joao, Torlasco, Camilla, Webber, Matthew, Dowsing, Benjamin, Hughes, Rebecca, Miranda, Inês, Witschey, Walter, Thompson, Elizabeth, Castelletti, Silvia, Crotti, Lia, Lovato, Luigi, Ponziani, Alberto, Moschonas, Konstantinos, Joy, George, Pierce, Iain, Kellman, Peter, Hughes, Alun, Biagini, Elena, Mohiddin, Saidi, Lopes, Luis, Ferrari, Victor, Litt, Harold, Captur, Gabriella, and Moon, James

Published
2023
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9. An International Multicenter Evaluation of Type 5 Long QT Syndrome

Author

Roberts, Jason D, Asaki, S Yukiko, Mazzanti, Andrea, Bos, J Martijn, Tuleta, Izabela, Muir, Alison R, Crotti, Lia, Krahn, Andrew D, Kutyifa, Valentina, Shoemaker, M Benjamin, Johnsrude, Christopher L, Aiba, Takeshi, Marcondes, Luciana, Baban, Anwar, Udupa, Sharmila, Dechert, Brynn, Fischbach, Peter, Knight, Linda M, Vittinghoff, Eric, Kukavica, Deni, Stallmeyer, Birgit, Giudicessi, John R, Spazzolini, Carla, Shimamoto, Keiko, Tadros, Rafik, Cadrin-Tourigny, Julia, Duff, Henry J, Simpson, Christopher S, Roston, Thomas M, Wijeyeratne, Yanushi D, El Hajjaji, Imane, Yousif, Maisoon D, Gula, Lorne J, Leong-Sit, Peter, Chavali, Nikhil, Landstrom, Andrew P, Marcus, Gregory M, Dittmann, Sven, Wilde, Arthur AM, Behr, Elijah R, Tfelt-Hansen, Jacob, Scheinman, Melvin M, Perez, Marco V, Kaski, Juan Pablo, Gow, Robert M, Drago, Fabrizio, Aziz, Peter F, Abrams, Dominic J, Gollob, Michael H, Skinner, Jonathan R, Shimizu, Wataru, Kaufman, Elizabeth S, Roden, Dan M, Zareba, Wojciech, Schwartz, Peter J, Schulze-Bahr, Eric, Etheridge, Susan P, Priori, Silvia G, and Ackerman, Michael J

Subjects
Genetics, Cardiovascular, Clinical Trials and Supportive Activities, Heart Disease, Clinical Research, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Adolescent, Adult, Death, Sudden, Cardiac, Electric Countershock, Electrocardiography, Female, Heart Arrest, Humans, Long QT Syndrome, Male, Middle Aged, Penetrance, Potassium Channels, Voltage-Gated, Registries, arrhythmia, genetics, long QT syndrome, penetrance, sudden cardiac death, Cardiorespiratory Medicine and Haematology, Clinical Sciences, Public Health and Health Services, Cardiovascular System & Hematology
Abstract

BackgroundInsight into type 5 long QT syndrome (LQT5) has been limited to case reports and small family series. Improved understanding of the clinical phenotype and genetic features associated with rare KCNE1 variants implicated in LQT5 was sought through an international multicenter collaboration.MethodsPatients with either presumed autosomal dominant LQT5 (N = 229) or the recessive Type 2 Jervell and Lange-Nielsen syndrome (N = 19) were enrolled from 22 genetic arrhythmia clinics and 4 registries from 9 countries. KCNE1 variants were evaluated for ECG penetrance (defined as QTc >460 ms on presenting ECG) and genotype-phenotype segregation. Multivariable Cox regression was used to compare the associations between clinical and genetic variables with a composite primary outcome of definite arrhythmic events, including appropriate implantable cardioverter-defibrillator shocks, aborted cardiac arrest, and sudden cardiac death.ResultsA total of 32 distinct KCNE1 rare variants were identified in 89 probands and 140 genotype positive family members with presumed LQT5 and an additional 19 Type 2 Jervell and Lange-Nielsen syndrome patients. Among presumed LQT5 patients, the mean QTc on presenting ECG was significantly longer in probands (476.9±38.6 ms) compared with genotype positive family members (441.8±30.9 ms, P

Published
2020

13. Molecular genetic testing in athletes: Why and when a position statement from the Italian Society of Sports Cardiology

Author

Castelletti, Silvia, Zorzi, Alessandro, Ballardini, Enrico, Basso, Cristina, Biffi, Alessandro, Brancati, Francesco, Cavarretta, Elena, Crotti, Lia, Contursi, Maurizio, D'Aleo, Antonio, D'Ascenzi, Flavio, Delise, Pietro, Dello Russo, Antonio, Gazale, Giovanni, Mos, Lucio, Novelli, Valeria, Palamà, Zefferino, Palermi, Stefano, Palmieri, Vincenzo, Patrizi, Giampiero, Pelliccia, Antonio, Pilichou, Kalliopi, Romano, Silvio, Sarto, Patrizio, Schwartz, Peter J., Tiberi, Monica, Zeppilli, Paolo, Corrado, Domenico, and Sciarra, Luigi

Published
2022
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14. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

Author

Wilde, Arthur A.M., Semsarian, Christopher, Márquez, Manlio F., Sepehri Shamloo, Alireza, Ackerman, Michael J., Ashley, Euan A., Sternick, Eduardo Back, Barajas-Martinez, Héctor, Behr, Elijah R., Bezzina, Connie R., Breckpot, Jeroen, Charron, Philippe, Chockalingam, Priya, Crotti, Lia, Gollob, Michael H., Lubitz, Steven, Makita, Naomasa, Ohno, Seiko, Ortiz-Genga, Martín, Sacilotto, Luciana, Schulze-Bahr, Eric, Shimizu, Wataru, Sotoodehnia, Nona, Tadros, Rafik, Ware, James S., Winlaw, David S., Kaufman, Elizabeth S., Aiba, Takeshi, Bollmann, Andreas, Choi, Jong-Il, Dalal, Aarti, Darrieux, Francisco, Giudicessi, John, Guerchicoff, Mariana, Hong, Kui, Krahn, Andrew D., MacIntyre, Ciorsti, Mackall, Judith A., Mont, Lluís, Napolitano, Carlo, Ochoa, Juan Pablo, Peichl, Petr, Pereira, Alexandre C., Schwartz, Peter J., Skinner, Jon, Stellbrink, Christoph, Tfelt-Hansen, Jacob, and Deneke, Thomas

Published
2022
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16. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Author

Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y., Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J., Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A., Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O., Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D., Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F., Cerrato, Natascia, Martins, Raphaël P., Campuzano, Oscar, Van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Clémenty, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noël, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K., Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P., Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B., Boukens, Bas J., Škorić-Milosavljević, Doris, Bikker, Hennie, Manevy, Federico C., Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Müller-Nurasyid, Martina, Veldink, Jan H., van den Berg, Leonard H., Van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Hervé, Chatel, Stéphanie, Karakachoff, Matilde, Bézieau, Stéphane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E., Cerrone, Marina, Chinitz, Larry A., Volders, Paul G., van de Berg, Maarten P., Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kääb, Stefan, Arnaout, Alain Al, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D., Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D., Mansourati, Jacques, Loeys, Bart, Leenhardt, Antoine, Guicheney, Pascale, Maury, Philippe, Schulze-Bahr, Eric, Robyns, Tomas, Breckpot, Jeroen, Babuty, Dominique, Priori, Silvia G., Napolitano, Carlo, de Asmundis, Carlo, Brugada, Pedro, Brugada, Ramon, Arbelo, Elena, Brugada, Josep, Mabo, Philippe, Behar, Nathalie, Giustetto, Carla, Molina, Maria Sabater, Gimeno, Juan R., Hasdemir, Can, Schwartz, Peter J., Crotti, Lia, McKeown, Pascal P., Sharma, Sanjay, Behr, Elijah R., Haissaguerre, Michel, Sacher, Frédéric, Rooryck, Caroline, Tan, Hanno L., Remme, Carol A., Postema, Pieter G., Delmar, Mario, Ellinor, Patrick T., Lubitz, Steven A., Gourraud, Jean-Baptiste, Tanck, Michael W., George, Jr., Alfred L., MacRae, Calum A., Burridge, Paul W., Dina, Christian, Probst, Vincent, Wilde, Arthur A., Schott, Jean-Jacques, Redon, Richard, and Bezzina, Connie R.

Published
2022
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19. Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation.

Author

Dusi, Veronica, Dagradi, Federica, Spazzolini, Carla, Crotti, Lia, Cerea, Paolo, Giovenzana, Fulvio L F, Musu, Giulia, Pedrazzini, Matteo, Torchio, Margherita, and Schwartz, Peter J

Abstract

Background and Aims Risk scores are proposed for genetic arrhythmias. Having proposed in 2010 one such score (M-FACT) for the long QT syndrome (LQTS), this study aims to test whether adherence to its suggestions would be appropriate. Methods LQT1/2/3 and genotype-negative patients without aborted cardiac arrest (ACA) before diagnosis or cardiac events (CEs) below age 1 were included in the study, focusing on an M-FACT score ≥2 (intermediate/high risk), either at presentation (static) or during follow-up (dynamic), previously associated with 40% risk of implantable cardioverter defibrillator (ICD) shocks within 4 years. Results Overall, 946 patients (26 ± 19 years at diagnosis, 51% female) were included. Beta-blocker (βB) therapy in 94% of them reduced the rate of those with a QTc ≥500 ms from 18% to 12% (P <.001). During 7 ± 6 years of follow-up, none died; 4% had CEs, including 0.4% with ACA. A static M-FACT ≥2 was present in 110 patients, of whom 106 received βBs. In 49/106 patients with persistent dynamic M-FACT ≥2, further therapeutic optimization (left cardiac sympathetic denervation in 55%, mexiletine in 31%, and ICD at 27%) resulted in just 7 (14%) patients with CEs (no ACA), with no CEs in the remaining 57. Additionally, 32 patients developed a dynamic M-FACT ≥2 but, after therapeutic optimization, only 3 (9%) had C Es. According to an M-FACT score ≥2, a total of 142 patients should have received an ICD, but only 22/142 (15%) were implanted, with shocks reported in 3. Conclusions Beta-blockers often shorten QTc, thus changing risk scores and ICD indications for primary prevention. Yearly risk reassessment with therapy optimization leads to fewer ICD implants (3%) without increasing life-threatening events. [ABSTRACT FROM AUTHOR]

Published
2024
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20. Implantable loop recorders in patients with Brugada syndrome: the BruLoop study

Author

Bergonti, Marco, primary, Sacher, Frederic, additional, Arbelo, Elena, additional, Crotti, Lia, additional, Sabbag, Avi, additional, Casella, Michela, additional, Saenen, Johan, additional, Rossi, Andrea, additional, Monaco, Cinzia, additional, Pannone, Luigi, additional, Compagnucci, Paolo, additional, Russo, Vincenzo, additional, Heller, Eyal, additional, Santoro, Amato, additional, Berne, Paola, additional, Bisignani, Antonio, additional, Baldi, Enrico, additional, Van Leuven, Olivier, additional, Migliore, Federico, additional, Marcon, Lorenzo, additional, Dagradi, Federica, additional, Sfondrini, Irene, additional, Landra, Federico, additional, Comune, Angelo, additional, Cespón-Fernández, María, additional, Nesti, Martina, additional, Santoro, Francesco, additional, Magnocavallo, Michele, additional, Vicentini, Alessandro, additional, Conti, Sergio, additional, Ribatti, Valentina, additional, Brugada, Pedro, additional, de Asmundis, Carlo, additional, Brugada, Josep, additional, Tondo, Claudio, additional, Schwartz, Peter J, additional, Haissaguerre, Michel, additional, Auricchio, Angelo, additional, and Conte, Giulio, additional

Published
2024
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21. Prognostic Value of Multiplexed Assays of Variant Effect and Automated Patch-clamping forKCNH2-LQTS Risk Stratification

Author

O’Neill, Matthew J., primary, Ng, Chai-Ann, additional, Aizawa, Takanori, additional, Sala, Luca, additional, Bains, Sahej, additional, Denjoy, Isabelle, additional, Winbo, Annika, additional, Ullah, Rizwan, additional, Shen, Qianyi, additional, Tan, Chek-Ying, additional, Kozek, Krystian, additional, Vanags, Loren R., additional, Mitchell, Devyn W., additional, Shen, Alex, additional, Wada, Yuko, additional, Kashiwa, Asami, additional, Crotti, Lia, additional, Dagradi, Federica, additional, Musu, Giulia, additional, Spazzolini, Carla, additional, Neves, Raquel, additional, Bos, J. Martijn, additional, Giudicessi, John R., additional, Bledsoe, Xavier, additional, Lancaster, Megan, additional, Glazer, Andrew M., additional, Roden, Dan M., additional, Leenhardt, Antoine, additional, Salem, Joe-Elie, additional, Earle, Nikki, additional, Stiles, Rachael, additional, Agee, Taylor, additional, Johnson, Christopher N., additional, Horie, Minoru, additional, Skinner, Jonathan, additional, Extramiana, Fabrice, additional, Ackerman, Michael J., additional, Schwartz, Peter J., additional, Ohno, Seiko, additional, Vandenberg, Jamie I., additional, and Kroncke, Brett M., additional

Published
2024
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24. A Primary Prevention Clinical Risk Score Model for Patients With Brugada Syndrome (BRUGADA-RISK)

Author

Honarbakhsh, Shohreh, Providencia, Rui, Garcia-Hernandez, Jorge, Martin, Claire A., Hunter, Ross J., Lim, Wei Y., Kirkby, Claire, Graham, Adam J., Sharifzadehgan, Ardalan, Waldmann, Victor, Marijon, Eloi, Munoz-Esparza, Carmen, Lacunza, Javier, Gimeno-Blanes, Juan Ramón, Ankou, Benedicte, Chevalier, Philippe, Antonio, Nátalia, Elvas, Luís, Castelletti, Silvia, Crotti, Lia, Schwartz, Peter, Scanavacca, Mauricio, Darrieux, Francisco, Sacilotto, Luciana, Mueller-Leisse, Johanna, Veltmann, Christian, Vicentini, Alessandro, Demarchi, Andrea, Cortez-Dias, Nuno, Antonio, Pedro Silverio, de Sousa, João, Adragao, Pedro, Cavaco, Diogo, Costa, Francisco Morosco, Khoueiry, Ziad, Boveda, Serge, Sousa, Mario João, Jebberi, Zeynab, Heck, Patrick, Mehta, Sarju, Conte, Giulio, Ozkartal, Tardu, Auricchio, Angelo, Lowe, Martin D., Schilling, Richard J., Prieto-Merino, David, and Lambiase, Pier D.

Published
2021
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25. Genetics of Adult and Fetal Forms of Long QT Syndrome

Author

Crotti, Lia, Ghidoni, Alice, Dagradi, Federica, Hecker, Markus, Editor-in-Chief, Backs, Johannes, Series Editor, Freichel, Marc, Series Editor, Korff, Thomas, Series Editor, Thomas, Dierk, Series Editor, Erdmann, Jeanette, editor, and Moretti, Alessandra, editor

Published
2019
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26. Real‐world candidacy to mavacamten in a contemporary hypertrophic obstructive cardiomyopathy population

Author

Bertero, Edoardo, primary, Chiti, Chiara, additional, Schiavo, Maria Alessandra, additional, Tini, Giacomo, additional, Costa, Paolo, additional, Todiere, Giancarlo, additional, Mabritto, Barbara, additional, Dei, Lorenzo‐Lupo, additional, Giannattasio, Alessia, additional, Mariani, Davide, additional, Lofiego, Carla, additional, Santolamazza, Caterina, additional, Monda, Emanuele, additional, Quarta, Giovanni, additional, Barbisan, Davide, additional, Mandoli, Giulia Elena, additional, Mapelli, Massimo, additional, Sguazzotti, Maurizio, additional, Negri, Francesco, additional, De Vecchi, Simona, additional, Ciabatti, Michele, additional, Tomasoni, Daniela, additional, Mazzanti, Andrea, additional, Marzo, Francesca, additional, de Gregorio, Cesare, additional, Raineri, Claudia, additional, Vianello, Pier Filippo, additional, Marchi, Alberto, additional, Biagioni, Giulia, additional, Insinna, Eleonora, additional, Parisi, Vanda, additional, Ditaranto, Raffaello, additional, Barison, Andrea, additional, Giammaresi, Andrea, additional, De Ferrari, Gaetano Maria, additional, Priori, Silvia, additional, Metra, Marco, additional, Pieroni, Maurizio, additional, Patti, Giuseppe, additional, Imazio, Massimo, additional, Perugini, Enrica, additional, Agostoni, Piergiuseppe, additional, Cameli, Matteo, additional, Merlo, Marco, additional, Sinagra, Gianfranco, additional, Senni, Michele, additional, Limongelli, Giuseppe, additional, Ammirati, Enrico, additional, Vagnarelli, Fabio, additional, Crotti, Lia, additional, Badano, Luigi, additional, Calore, Chiara, additional, Gabrielli, Domenico, additional, Re, Federica, additional, Musumeci, Giuseppe, additional, Emdin, Michele, additional, Barbato, Emanuele, additional, Musumeci, Beatrice, additional, Autore, Camillo, additional, Biagini, Elena, additional, Porto, Italo, additional, Olivotto, Iacopo, additional, and Canepa, Marco, additional

Published
2023
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27. Corrigendum to ‘Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management’ [International Journal of Cardiology, 2023, 41:180–186]

Author

Brignole, Michele, primary, Cecchi, Franco, additional, Anastasakis, Aris, additional, Crotti, Lia, additional, Deharo, Jean Claude, additional, Elliott, Perry M., additional, Fedorowski, Artur, additional, Kaski, Juan Pablo, additional, Limongelli, Giuseppe, additional, Maron, Martin S., additional, Olivotto, Iacopo, additional, Ommen, Steve R., additional, Parati, Gianfranco, additional, Shen, Win, additional, Ungar, Andrea, additional, and Wilde, Arthur, additional

Published
2023
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28. ECG/echo indexes in the diagnostic approach to amyloid cardiomyopathy: A head-to-head comparison from the AC-TIVE study

Author

Pagura, Linda, primary, Porcari, Aldostefano, additional, Cameli, Matteo, additional, Biagini, Elena, additional, Canepa, Marco, additional, Crotti, Lia, additional, Imazio, Massimo, additional, Forleo, Cinzia, additional, Pavasini, Rita, additional, Limongelli, Giuseppe, additional, Perlini, Stefano, additional, Metra, Marco, additional, Boriani, Giuseppe, additional, Emdin, Michele, additional, Sinagra, Gianfranco, additional, Merlo, Marco, additional, Longo, Francesca, additional, Rossi, Maddalena, additional, Varrà, Guerino Giuseppe, additional, Saro, Riccardo, additional, Dore, Franca, additional, Girardi, Francesca, additional, Vergaro, Giuseppe, additional, Musumeci, Beatrice, additional, Autore, Camillo, additional, Cappelli, Francesco, additional, Perfetto, Federico, additional, Olivotto, Iacopo, additional, Favale, Stefano, additional, Carella, Maria Cristina, additional, Guaricci, Andrea Igoren, additional, Ciccone, Marco Matteo, additional, Di Bella, Gianluca, additional, Tomasoni, Daniela, additional, Rella, Valeria, additional, Branzi, Giovanna, additional, Badano, Luigi, additional, Parati, Gianfranco, additional, Palmiero, Giuseppe, additional, Caiazza, Martina, additional, Caponetti, Angelo Giuseppe, additional, Saturi, Giulia, additional, Labate, Marianna Eleonora, additional, Andreis, Alessandro, additional, Paneva, Elena, additional, De Ferrari, Gaetano Maria, additional, Di Ienno, Luca, additional, De Carli, Giuseppe, additional, Giacomin, Elisa, additional, and Arzilli, Chiara, additional

Published
2023
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29. Long and Short QT Syndromes

Author

Crotti, Lia, Kotta, Maria-Christina, Castelletti, Silvia, Hecker, Markus, Editor-in-Chief, Backs, Johannes, Series Editor, Freichel, Marc, Series Editor, Korff, Thomas, Series Editor, Thomas, Dierk, Series Editor, and Remme, Carol Ann, editor

Published
2018
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30. Author Correction: Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Author

Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Chiang, David Y., Jouni, Mariam, Simonet, Floriane, Jurgens, Sean J., Baudic, Manon, Nicastro, Michele, Potet, Franck, Offerhaus, Joost A., Walsh, Roddy, Choi, Seung Hoan, Verkerk, Arie O., Mizusawa, Yuka, Anys, Soraya, Minois, Damien, Arnaud, Marine, Duchateau, Josselin, Wijeyeratne, Yanushi D., Muir, Alison, Papadakis, Michael, Castelletti, Silvia, Torchio, Margherita, Ortuño, Cristina Gil, Lacunza, Javier, Giachino, Daniela F., Cerrato, Natascia, Martins, Raphaël P., Campuzano, Oscar, Van Dooren, Sonia, Thollet, Aurélie, Kyndt, Florence, Mazzanti, Andrea, Clémenty, Nicolas, Bisson, Arnaud, Corveleyn, Anniek, Stallmeyer, Birgit, Dittmann, Sven, Saenen, Johan, Noël, Antoine, Honarbakhsh, Shohreh, Rudic, Boris, Marzak, Halim, Rowe, Matthew K., Federspiel, Claire, Le Page, Sophie, Placide, Leslie, Milhem, Antoine, Barajas-Martinez, Hector, Beckmann, Britt-Maria, Krapels, Ingrid P., Steinfurt, Johannes, Winkel, Bo Gregers, Jabbari, Reza, Shoemaker, Moore B., Boukens, Bas J., Škorić-Milosavljević, Doris, Bikker, Hennie, Manevy, Federico, Lichtner, Peter, Ribasés, Marta, Meitinger, Thomas, Müller-Nurasyid, Martina, Veldink, Jan H., van den Berg, Leonard H., Van Damme, Philip, Cusi, Daniele, Lanzani, Chiara, Rigade, Sidwell, Charpentier, Eric, Baron, Estelle, Bonnaud, Stéphanie, Lecointe, Simon, Donnart, Audrey, Le Marec, Hervé, Chatel, Stéphanie, Karakachoff, Matilde, Bézieau, Stéphane, London, Barry, Tfelt-Hansen, Jacob, Roden, Dan, Odening, Katja E., Cerrone, Marina, Chinitz, Larry A., Volders, Paul G., van de Berg, Maarten P., Laurent, Gabriel, Faivre, Laurence, Antzelevitch, Charles, Kääb, Stefan, Arnaout, Alain Al, Dupuis, Jean-Marc, Pasquie, Jean-Luc, Billon, Olivier, Roberts, Jason D., Jesel, Laurence, Borggrefe, Martin, Lambiase, Pier D., Mansourati, Jacques, Loeys, Bart, Leenhardt, Antoine, Guicheney, Pascale, Maury, Philippe, Schulze-Bahr, Eric, Robyns, Tomas, Breckpot, Jeroen, Babuty, Dominique, Priori, Silvia G., Napolitano, Carlo, de Asmundis, Carlo, Brugada, Pedro, Brugada, Ramon, Arbelo, Elena, Brugada, Josep, Mabo, Philippe, Behar, Nathalie, Giustetto, Carla, Molina, Maria Sabater, Gimeno, Juan R., Hasdemir, Can, Schwartz, Peter J., Crotti, Lia, McKeown, Pascal P., Sharma, Sanjay, Behr, Elijah R., Haissaguerre, Michel, Sacher, Frédéric, Rooryck, Caroline, Tan, Hanno L., Remme, Carol A., Postema, Pieter G., Delmar, Mario, Ellinor, Patrick T., Lubitz, Steven A., Gourraud, Jean-Baptiste, Tanck, Michael W., George, Jr., Alfred L., MacRae, Calum A., Burridge, Paul W., Dina, Christian, Probst, Vincent, Wilde, Arthur A., Schott, Jean-Jacques, Redon, Richard, and Bezzina, Connie R.

Published
2022
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33. Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Author

Crotti, Lia, primary, Spazzolini, Carla, additional, Nyegaard, Mette, additional, Overgaard, Michael T, additional, Kotta, Maria-Christina, additional, Dagradi, Federica, additional, Sala, Luca, additional, Aiba, Takeshi, additional, Ayers, Mark D, additional, Baban, Anwar, additional, Barc, Julien, additional, Beach, Cheyenne M, additional, Behr, Elijah R, additional, Bos, J Martijn, additional, Cerrone, Marina, additional, Covi, Peter, additional, Cuneo, Bettina, additional, Denjoy, Isabelle, additional, Donner, Birgit, additional, Elbert, Adrienne, additional, Eliasson, Håkan, additional, Etheridge, Susan P, additional, Fukuyama, Megumi, additional, Girolami, Francesca, additional, Hamilton, Robert, additional, Horie, Minoru, additional, Iascone, Maria, additional, Jaimez, Juan Jiménez, additional, Jensen, Henrik Kjærulf, additional, Kannankeril, Prince J, additional, Kaski, Juan P, additional, Makita, Naomasa, additional, Muñoz-Esparza, Carmen, additional, Odland, Hans H, additional, Ohno, Seiko, additional, Papagiannis, John, additional, Porretta, Alessandra Pia, additional, Prandstetter, Christopher, additional, Probst, Vincent, additional, Robyns, Tomas, additional, Rosenthal, Eric, additional, Rosés-Noguer, Ferran, additional, Sekarski, Nicole, additional, Singh, Anoop, additional, Spentzou, Georgia, additional, Stute, Fridrike, additional, Tfelt-Hansen, Jacob, additional, Till, Jan, additional, Tobert, Kathryn E, additional, Vinocur, Jeffrey M, additional, Webster, Gregory, additional, Wilde, Arthur A M, additional, Wolf, Cordula M, additional, Ackerman, Michael J, additional, and Schwartz, Peter J, additional

Published
2023
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41. Corrigendum to ‘Syncope in hypertrophic cardiomyopathy (part II): An expert consensus statement on the diagnosis and management’ [International Journal of Cardiology, 2023, 41:180–186]

Author

Brignole, Michele, Cecchi, Franco, Anastasakis, Aris, Crotti, Lia, Deharo, Jean Claude, Elliott, Perry M., Fedorowski, Artur, Kaski, Juan Pablo, Limongelli, Giuseppe, Maron, Martin S., Olivotto, Iacopo, Ommen, Steve R., Parati, Gianfranco, Shen, Win, Ungar, Andrea, and Wilde, Arthur

Published
2024
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42. [Rationale and significance of the Italian Network for Cardiac Amyloidosis]

Author

Sinagra, Gianfranco, Emdin, Michele, Merlo, Marco, Vergaro, Giuseppe, Aimo, Alberto, Biagini, Elena, Imazio, Massimo, Porcari, Aldostefano, Limongelli, Giuseppe, Cipriani, Alberto, Canepa, Marco, Musumeci, Beatrice, Cameli, Matteo, Crotti, Lia, Di Bella, Gianluca, Di Lenarda, Andrea, Cappelli, Francesco, Chimenti, Cristina, Obici, Laura, Iacoviello, Massimo, Perlini, Stefano, Pieroni, Maurizio, Metra, Marco, Oliva, Fabrizio, Perrone Filardi, Pasquale, Colivicchi, Furio, Indolfi, Ciro, Sinagra, Gianfranco, Emdin, Michele, Merlo, Marco, Vergaro, Giuseppe, Aimo, Alberto, Biagini, Elena, Imazio, Massimo, Porcari, Aldostefano, Limongelli, Giuseppe, Cipriani, Alberto, Canepa, Marco, Musumeci, Beatrice, Cameli, Matteo, Crotti, Lia, Di Bella, Gianluca, Di Lenarda, Andrea, Cappelli, Francesco, Chimenti, Cristina, Obici, Laura, Iacoviello, Massimo, Perlini, Stefano, Pieroni, Maurizio, Metra, Marco, Oliva, Fabrizio, Perrone Filardi, Pasquale, Colivicchi, Furio, and Indolfi, Ciro

Abstract

The perspective on amyloidosis has changed deeply over the last 10 years following major advances in diagnosis and treatment options, especially in cardiac amyloidosis. This intrinsically heterogeneous disease exposes to the risk of fragmentation of knowledge and requires the interaction among experts of different specialties and subspecialties. Suspicion of disease, timely recognition and confirmation of final diagnosis, prognostic stratification, clinical management and therapeutic strategies represent essential steps to be taken. Missing or delaying the diagnosis may have dramatic impact on patient outcome, as in the case of chemotherapy in unrecognized light-chain amyloidosis. Therefore, there is an urgent need for the foundation of an Italian Amyloidosis Network to deal with the challenges of this condition and orient clinical management at national and local levels. The present consensus document aims to provide the rationale and scopes of the Italian Amyloidosis Network, which has been conceived as an organizational framework for professionals managing patients with amyloidosis.

Published
2023

43. Razionale e valore fondamentale della Rete Italiana integrata dell’Amiloidosi Cardiaca

Author

Sinagra, Gianfranco, Emdin, Michele, Merlo, Marco, Vergaro, Giuseppe, Aimo, Alberto, Biagini, Elena, Imazio, Massimo, Porcari, Aldostefano, Limongelli, Giuseppe, Cipriani, Alberto, Canepa, Marco, Musumeci, Beatrice, Cameli, Matteo, Crotti, Lia, Di Bella, Gianluca, Di Lenarda, Andrea, Cappelli, Francesco, Chimenti, Cristina, Obici, Laura, Iacoviello, Massimo, Perlini, Stefano, Pieroni, Maurizio, Metra, Marco, Oliva, Fabrizio, Perrone Filardi, Pasquale, Colivicchi, Furio, Indolfi, Ciro, Sinagra, Gianfranco, Emdin, Michele, Merlo, Marco, Vergaro, Giuseppe, Aimo, Alberto, Biagini, Elena, Imazio, Massimo, Porcari, Aldostefano, Limongelli, Giuseppe, Cipriani, Alberto, Canepa, Marco, Musumeci, Beatrice, Cameli, Matteo, Crotti, Lia, Di Bella, Gianluca, Di Lenarda, Andrea, Cappelli, Francesco, Chimenti, Cristina, Obici, Laura, Iacoviello, Massimo, Perlini, Stefano, Pieroni, Maurizio, Metra, Marco, Oliva, Fabrizio, Perrone Filardi, Pasquale, Colivicchi, Furio, and Indolfi, Ciro

Subjects
Treatment, Clinical management, Cardiac amyloidosi, Differential diagnosi, Perspective, Differential diagnosis, Cardiac amyloidosis, Perspectives
Abstract

The perspective on amyloidosis has changed deeply over the last 10 years following major advances in diagnosis and treatment options, especially in cardiac amyloidosis. This intrinsically heterogeneous disease exposes to the risk of fragmentation of knowledge and requires the interaction among experts of different specialties and subspecialties. Suspicion of disease, timely recognition and confirmation of final diagnosis, prognostic stratification, clinical management and therapeutic strategies represent essential steps to be taken. Missing or delaying the diagnosis may have dramatic impact on patient outcome, as in the case of chemotherapy in unrecognized light-chain amyloidosis. Therefore, there is an urgent need for the foun- dation of an Italian Amyloidosis Network to deal with the challenges of this condition and orient clinical management at national and local levels. The present consensus document aims to provide the rationale and scopes of the Italian Amyloidosis Network, which has been conceived as an organizational framework for professionals managing patients with amyloidosis.

Published
2023

44. EN-452414-5 VENTRICULAR CONDUCTION IS A MARKER FOR ARRHYTHMIC RISK IN OVERLAP SODIUM CHANNEL DISEASE

Author

Wijeyeratne, Yanushi D., primary, Tanck, Michael, additional, Barc, Julien, additional, Muir, Alison, additional, Aiba, Takeshi, additional, Bos, Johan M., additional, Veltmann, Christian, additional, Galvin, Joseph M., additional, Crotti, Lia, additional, Ishikawa, Taisuke, additional, Ohno, Seiko, additional, Page, Stephen, additional, Denjoy, Isabelle, additional, Tester, David, additional, Muggenthaler, Martina, additional, Takahashi, Kazuhiro, additional, Raju, Hari, additional, GOURRAUD, JEAN BAPTISTE, additional, Redon, Richard, additional, Schott, Jean-Jacques, additional, Kyndt, Florence, additional, Haglund-Turnquist, Carla, additional, Pedrazzini, Matteo, additional, Torchio, Margherita, additional, Dagradi, Frederica, additional, Papadakis, Michael, additional, Sharma, Sanjay, additional, Petzer, Edward, additional, Roden, Dan M., additional, Horie, Minoru, additional, Schwartz, Peter J., additional, Makita, Naomasa, additional, Borggrefe, Martin M., additional, Ackerman, Michael J., additional, Shimizu, Wataru, additional, McKeown, Pascal, additional, PROBST, VINCENT, additional, and Behr, Elijah, additional

Published
2023
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45. From the phenotype to precision medicine: an update on the cardiomyopathies diagnostic workflow

Author

Autore, Camillo, primary, Bariani, Riccardo, additional, Bauce, Barbara, additional, Biagini, Elena, additional, Canepa, Marco, additional, Castelletti, Silvia, additional, Crotti, Lia, additional, Limongelli, Giuseppe, additional, Merlo, Marco, additional, Monda, Emanuele, additional, Pio Loco detto Gava, Carola, additional, Parisi, Vanda, additional, Tini, Giacomo, additional, and Imazio, Massimo, additional

Published
2023
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46. Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2

Author

Giannetti, Federica, primary, Barbieri, Miriam, additional, Shiti, Assad, additional, Casini, Simona, additional, Sager, Philip T, additional, Das, Saumya, additional, Pradhananga, Sabindra, additional, Srinivasan, Dinesh, additional, Nimani, Saranda, additional, Alerni, Nicolò, additional, Louradour, Julien, additional, Mura, Manuela, additional, Gnecchi, Massimiliano, additional, Brink, Paul, additional, Zehender, Manfred, additional, Koren, Gideon, additional, Zaza, Antonio, additional, Crotti, Lia, additional, Wilde, Arthur A M, additional, Schwartz, Peter J, additional, Remme, Carol Ann, additional, Gepstein, Lior, additional, Sala, Luca, additional, and Odening, Katja E, additional

Published
2023
Full Text
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