Repositorio Dspace

Listar por autor "Wahbi, Karim"

Listar por autor "Wahbi, Karim"

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  • Clinical Features and Outcomes of Pediatric MYH7-Related Dilated Cardiomyopathy 
    de-Frutos, Fernando; Ochoa, Juan-Pablo; Webster, Gregory; Jansen, Mark; Remior, Paloma; Rasmussen, Torsten-B; Sabater-Molina, María; Barriales-Villa, Roberto; Girolami, Francesca; Cesar, Sergi; Fuentes-Cañamero, María-Eugenia; Álvarez-García-Roves, Reyes; Wahbi, Karim; Limeres, Javier; Kubanek, Milos; Slieker, Martijn-G; Sarquella-Brugada, Georgia; Abrams, Dominic-J; Dooijes, Dennis; Domínguez, Fernando; García-Pavia, Pablo (WILEY, 2024-11)
    BACKGROUND: Although genetic variants in MYH7 are the most frequent cause of pediatric genetic dilated cardiomyopathy (DCM), there are no studies available describing this entity. We sought to describe clinical features, ...
  • Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator 
    Protonotarios, Alexandros; Bariani, Riccardo; Cappelletto, Chiara; Pavlou, Menelaos; García-García, Alba; Cipriani, Alberto; Protonotarios, Ioannis; Rivas, Adrian; Wittenberg, Regitze; Graziosi, Maddalena; Xylouri, Zafeirenia; Larranaga-Moreira, José-M; de-Luca, Antonio; Celeghin, Rudy; Pilichou, Kalliopi; Bakalakos, Athanasios; Lopes, Luis-Rocha; Savvatis, Konstantinos; Stolfo, Davide; Dal-Ferro, Matteo; Merlo, Marco; Basso, Cristina; Limeres-Freire, Javier; Rodríguez-Palomares, José-F; Kubo, Toru; Ripoll-Vera, Tomás; Barriales-Villa, Roberto; Antoniades, Loizos; Mogensen, Jens; García-Pavia, Pablo; Wahbi, Karim; Biagini, Elena; Anastasakis, Aris; Tsatsopoulou, Adalena; Zorio, Esther; Gimeno-Blanes, Juan-Ramon; Manuel-García-Pinilla, José; Syrris, Petros; Sinagra, Gianfranco; Bauce, Barbara; Elliott, Perry-M (OXFORD UNIV PRESS, 2022-08-21)
    AIMS: To study the impact of genotype on the performance of the 2019 risk model for arrhythmogenic right ventricular cardiomyopathy (ARVC). METHODS AND RESULTS: The study cohort comprised 554 patients with a definite ...
  • Natural History of MYH7-Related Dilated Cardiomyopathy 
    de-Frutos, Fernando; Pablo-Ochoa, Juan; Navarro-Peñalver, Marina; Baas, Annette; Bjerre, Jesper-Vandborg; Zorio, Esther; Méndez, Irene; Lorca, Rebeca; Verdonschot, Job-AJ; Elpidio-García-Granja, Pablo; Bilinska, Zofia; Fatkin, Diane; Fuentes-Cañamero, María-Eugenia; García-Pinilla, José-Manuel; García-Álvarez, María-I; Girolami, Francesca; Barriales-Villa, Roberto; Díez-López, Carles; Lopes, Luis-R; Wahbi, Karim; García-Álvarez, Ana; Rodríguez-Sánchez, Ibon; Rekondo-Olaetxea, Javier; Rodríguez-Palomares, José-F; Gallego-Delgado, María; Meder, Benjamin; Kubanek, Milos; Hansen, Frederikke-G; Alejandra-Restrepo-Cordoba, María; Palomino-Doza, Julián; Ruiz-Guerrero, Luis; Sarquella-Brugada, Georgia; Pérez-Pérez, Alberto; Bermúdez-Jiménez, Francisco-José; Ripoll-Vera, Tomás; Rasmussen, Torsten-B; Jansen, Mark; Sabater-Molina, María; Elliot, Perry-M; García-Pavia, Pablo (ELSEVIER SCIENCE INC, 2022-10)
    BACKGROUND: Variants in myosin heavy chain 7 (MYH7) are responsible for disease in 1% to 5% of patients with dilated cardiomyopathy (DCM); however, the clinical characteristics and natural history of MYH7-related DCM are ...
  • Risks of Ventricular Arrhythmia and Heart Failure in Carriers of RBM20 Variants 
    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-Penalver, Marina; Crespo-Leiro, María-G; Larranaga-Moreira, José-M; de-Frutos, Fernando; Johnson, Renee; Slater, Thomas-A; Monserrat, Lorenzo; Sengupta, Anshuman; Mestroni, Luisa; Taylor, Matthew-RG; Sinagra, Gianfranco; Bilinska, Zofia; Solla-Ruiz, Itziar; Arana-Achaga, Xabier; Barriales-Villa, Roberto; García-Pavia, Pablo; Gimeno-Blanes, Juan-Ramón; Dal-Ferro, Matteo; Merlo, Marco; Wahbi, Karim; Fatkin, Diane; Mogensen, Jens; Rasmussen, Torsten-B; Elliott, Perry-M (LIPPINCOTT WILLIAMS & WILKINS, 2023-10)
    BACKGROUND: Variants in RBM20 are reported in 2% to 6% of familial cases of dilated cardiomyopathy and may be associated with fatal ventricular arrhythmia and rapid heart failure progression. We sought to determine the ...