How far should guidelines be followed?

por Rapezzi, Claudio, Lorenzini, Massimiliano
Publicado 2020

The complex interplay between fitness, genetics, lifestyle, and inflammation in the pathogenesis of coronary atherosclerosis: lessons from the Amazon rainforest

por Ditaranto, Raffaello, Vitale, Giovanni, Lorenzini, Massimiliano, Rapezzi, Claudio
Publicado 2019

Diagnostic performance of imaging investigations in detecting and differentiating cardiac amyloidosis: a systematic review and meta‐analysis

por Brownrigg, Jack, Lorenzini, Massimiliano, Lumley, Matthew, Elliott, Perry
Publicado 2019

Coexistence of degenerative aortic stenosis and wild type transthyretin-related cardiac amyloidosis: a potentially dangerous association that can be non-invasively identified

por Longhi, Simone, Milandri, Agnese, Gagliardi, Christian, Lorenzini, Massimiliano, Saia, Francesco, Leone, Ornella, Guidalotti, Pier Luigi, Rapezzi, Claudio
Publicado 2015

Isolated aortic root dilation in homocystinuria

por Lorenzini, Massimiliano, Guha, Nishan, Davison, James E., Pitcher, Alex, Pandya, Bejal, Kemp, Helena, Lachmann, Robin, Elliott, Perry M., Murphy, Elaine
Publicado 2017

Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers

por Lorenzini, Massimiliano, Norrish, Gabrielle, Field, Ella, Ochoa, Juan Pablo, Cicerchia, Marcos, Akhtar, Mohammed M., Syrris, Petros, Lopes, Luis R., Kaski, Juan Pablo, Elliott, Perry M.
Publicado 2020

Effects of myocardial fibrosis assessed by MRI on dynamic left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy: a retrospective database analysis

por Biagini, Elena, Lorenzini, Massimiliano, Olivotto, Iacopo, Rocchi, Guido, Lovato, Luigi, Lai, Francesco, Rosmini, Stefania, Pazzi, Chiara, Pasquale, Ferdinando, Reggiani, Maria Letizia Bacchi, Fattori, Rossella, Rapezzi, Claudio
Publicado 2012

Differences in cardiac phenotype and natural history of laminopathies with and without neuromuscular onset

por Ditaranto, Raffaello, Boriani, Giuseppe, Biffi, Mauro, Lorenzini, Massimiliano, Graziosi, Maddalena, Ziacchi, Matteo, Pasquale, Ferdinando, Vitale, Giovanni, Berardini, Alessandra, Rinaldi, Rita, Lattanzi, Giovanna, Potena, Luciano, Martin Suarez, Sofia, Bacchi Reggiani, Maria Letizia, Rapezzi, Claudio, Biagini, Elena
Publicado 2019

ESC EORP Cardiomyopathy Registry: real‐life practice of genetic counselling and testing in adult cardiomyopathy patients

por Heliö, Tiina, Elliott, Perry, Koskenvuo, Juha W., Gimeno, Juan R., Tavazzi, Luigi, Tendera, Michal, Kaski, Juan Pablo, Mansencal, Nicolas, Bilińska, Zofia, Carr‐White, Gerry, Damy, Thibaud, Frustaci, Andrea, Kindermann, Ingrid, Ripoll‐Vera, Tomas, Čelutkienė, Jelena, Axelsson, Anna, Lorenzini, Massimiliano, Saad, Aly, Maggioni, Aldo P., Laroche, Cécile, Caforio, Alida L.P., Charron, Philippe
Publicado 2020

Microstructural and Microvascular Phenotype of Sarcomere Mutation Carriers and Overt Hypertrophic Cardiomyopathy

por Joy, George, Kelly, Christopher I., Webber, Matthew, Pierce, Iain, Teh, Irvin, McGrath, Louise, Velazquez, Paula, Hughes, Rebecca K., Kotwal, Huafrin, Das, Arka, Chan, Fiona, Bakalakos, Athanasios, Lorenzini, Massimiliano, Savvatis, Konstantinos, Mohiddin, Saidi A., Macfarlane, Peter W., Orini, Michele, Manisty, Charlotte, Kellman, Peter, Davies, Rhodri H., Lambiase, Pier D., Nguyen, Christopher, Schneider, Jurgen E., Tome, Maite, Captur, Gabriella, Dall’Armellina, Erica, Moon, James C., Lopes, Luis R.
Publicado 2023

Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants

por Cannie, Douglas E., Protonotarios, Alexandros, Bakalakos, Athanasios, Syrris, Petros, Lorenzini, Massimiliano, De Stavola, Bianca, Bjerregaard, Louise, Dybro, Anne M., Hey, Thomas M., Hansen, Frederikke G., Navarro Peñalver, Marina, Crespo-Leiro, Maria G., Larrañaga-Moreira, Jose M., de Frutos, Fernando, Johnson, Renee, Slater, Thomas A., Monserrat, Lorenzo, Sengupta, Anshuman, Mestroni, Luisa, Taylor, Matthew R.G., Sinagra, Gianfranco, Bilinska, Zofia, Solla-Ruiz, Itziar, Arana Achaga, Xabier, Barriales-Villa, Roberto, Garcia-Pavia, Pablo, Gimeno, Juan R., Dal Ferro, Matteo, Merlo, Marco, Wahbi, Karim, Fatkin, Diane, Mogensen, Jens, Rasmussen, Torsten B., Elliott, Perry M.
Publicado 2023

Alpha-protein kinase 3 (ALPK3) truncating variants are a cause of autosomal dominant hypertrophic cardiomyopathy

por Lopes, Luis R, Garcia-Hernández, Soledad, Lorenzini, Massimiliano, Futema, Marta, Chumakova, Olga, Zateyshchikov, Dmitry, Isidoro-Garcia, Maria, Villacorta, Eduardo, Escobar-Lopez, Luis, Garcia-Pavia, Pablo, Bilbao, Raquel, Dobarro, David, Sandin-Fuentes, Maria, Catalli, Claudio, Gener Querol, Blanca, Mezcua, Ainhoa, Garcia Pinilla, Jose, Bloch Rasmussen, Torsten, Ferreira-Aguar, Ana, Revilla-Martí, Pablo, Basurte Elorz, Maria Teresa, Bautista Paves, Alicia, Ramon Gimeno, Juan, Figueroa, Ana Virginia, Franco-Gutierrez, Raul, Fuentes-Cañamero, Maria Eugenia, Martinez Moreno, Marina, Ortiz-Genga, Martin, Piqueras-Flores, Jesus, Analia Ramos, Karina, Rudzitis, Ainars, Ruiz-Guerrero, Luis, Stein, Ricardo, Triguero-Bocharán, Mayte, de la Higuera, Luis, Ochoa, Juan Pablo, Abu-Bonsrah, Dad, Kwok, Cecilia Y T, Smith, Jacob B, Porrello, Enzo R, Akhtar, Mohammed M, Jager, Joanna, Ashworth, Michael, Syrris, Petros, Elliott, David A, Monserrat, Lorenzo, Elliott, Perry M
Publicado 2021