Browsing by Author "Barriales-Villa, Roberto"
Now showing items 1-5 of 5
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Clinical phenotypes and prognosis of dilated cardiomyopathy caused by truncating variants in the TTN Gene. Akhtar, Mohammed Majid; Lorenzini, Massimiliano; Cicerchia, Marcos; Ochoa, Juan Pablo; Hey, Thomas Morris; Sabater Molina, Maria; Restrepo-Cordoba, Maria Alejandra; Dal Ferro, Matteo; Stolfo, Davide; Johnson, Renee; Larrañaga-Moreira, José M.; Robles-Mezcua, Ainhoa; Rodriguez-Palomares, Jose F.; Casas, Guillem; Peña-Peña, Maria Luisa; Lopes, Luis Rocha; Gallego-Delgado, Maria; Franaszczyk, Maria; Laucey, Gemma; Rangel-Sousa, Diego; Basurte, Mayte; Palomino-Doza, Julian; Villacorta, Eduardo; Bilinska, Zofia; Limeres Freire, Javier; Garcia Pinilla, José M. José M.; Barriales-Villa, Roberto; Fatkin, Diane; Sinagra, Gianfranco; García Pavía, Pablo
; Gimeno, Juan R.; Mogensen, Jens; Monserrat, Lorenzo; Elliott, Perry M. (Circulation: Heart Failure, 2020)
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Direct oral anticoagulants in patients with hypertrophic cardiomyopathy and atrial fibrillation. Domínguez, Fernando; Climent, Vicente; Zorio, Esther; Ripoll Vera, Tomás; Salazar Mendiguchía, Joel; García Pinilla, José Manuel; Urbano Moral, José Ángel; Fernández Fernández, Xusto; López Cuenca, David; Ajo Ferrer, Raquel; Sanz Sánchez, Jorge; Gómez Pérez, Yolanda; López Garrido, Miguel A.; Barriales Villa, Roberto; Gimeno, Juan Ramón; García Pavía, Pablo (International Journal of Cardiology, 2017)
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Mavacamten for treatment of symptomatic obstructive hypertrophic cardiomyopathy (EXPLORER-HCM): a randomised, double-blind, placebo-controlled, phase 3 trial. Olivotto, Iacopo; Oreziak, Artur; Barriales Villa, Roberto; Abraham, Theodore P.; Masri, Ahmad; García Pavía, Pablo; Jacoby, Daniel (The Lancet, 2020)
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Negative screening of Fabry disease in patients with conduction disorders requiring a pacemaker. López-Sainz, Ángela; Climent, Vicente; Ripoll-Vera, Tomas; Espinosa, Maria Angeles; Barriales-Villa, Roberto; Navarro, Marina; Limeres, Javier; Domingo, Diana; Kasper, David C.; García Pavía, Pablo (Orphanet Journal of Rare Diseases, 2019)
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Truncating FLNC mutations are associated with high-risk dilated and arrhythmogenic cardiomyopathies. Ortiz-Genga, Martín F.; Cuenca, Sofía; Dal Ferro, Matteo; Zorio, Esther; Salgado-Aranda, Ricardo; Climent, Vicente; Padrón-Barthe, Laura; Duro-Aguado, Iria; Jiménez-Jáimez, Juan; Hidalgo-Olivares, Víctor M.; García-Campo, Enrique; Lanzillo, Chiara; Suárez-Mier, Mª Paz; Yonath, Hagith; Marcos-Alonso, Sonia; Ochoa, Juan P.; Santomé, José L.; García-Giustiniani, Diego; Rodríguez-Garrido, Jorge L.; Domínguez, Fernando; Merlo, Marco; Palomino, Julián; Peña, María L.; Trujillo, Juan P.; Martín-Vila, Alicia; Stolfo, Davide; Molina, Pilar; Lara-Pezzi, Enrique; Calvo, Francisco; Nof, Eyal; Calò, Leonardo; Barriales Villa, Roberto; Gimeno-Blanes, Juan R.; Arad, Michael; García Pavía, Pablo; Montserrat, Lorenzo (Journal of the American College of Cardiology, 2016)