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Journal Article
Revista Espanola de Cardiologia, ISSN 0300-8932, 2008, Volume 61, Issue 2, pp. 112 - 115
Journal Article
Insights into Imaging, ISSN 1869-4101, 12/2018, Volume 9, Issue 6, pp. 1007 - 1020
The purpose of this article is to review how cardiac MRI provides the clinician with detailed information about the hypertrophic cardiomyopathy (HCM)... 
Heart | Hypertrophic cardiomyopathy | Phenotypes | Magnetic resonance | Development and progression | Phenotype | Genetic aspects | Cardiomyopathy, Hypertrophic | Magnetic resonance imaging | Cardiology | Remodeling | Morphology | Stretching | Eutrophication
Journal Article
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2457 - 2467
Journal Article
Journal Article
PLoS ONE, ISSN 1932-6203, 04/2016, Volume 11, Issue 4, p. e0153851
Journal Article
by Domínguez, Fernando and Cuenca, Sofía and Bilińska, Zofia and Toro, Rocío and Toro, Rocio and Villard, Eric and Barriales-Villa, Roberto and Ochoa, Juan Pablo and Asselbergs, Folkert and Sammani, Arjan and Franaszczyk, Maria and Akhtar, Mohammed and Coronado-Albi, Maria José and Rangel-Sousa, Diego and Rodriguez-Palomares, Jose F and Jiménez-Jáimez, Juan and Garcia-Pinilla, José Manuel and Garcia-Pinilla, Jose Manuel and Ripoll-Vera, Tomás and Mogollón-Jiménez, Maria Victoria and Fontalba-Romero, Ana and Garcia-Medina, Dolores and Palomino-Doza, Julian and de Gonzalo-Calvo, David and Cicerchia, Marcos and Salazar-Mendiguchia, Joel and Salas, Clara and Pankuweit, Sabine and Hey, Thomas Morris and Mogensen, Jens and Barton, Paul J and Charron, Philippe and Elliott, Perry and Elliott, Perry M and Garcia-Pavia, Pablo and Eiskjær, Hans and Barriales, Roberto and Fernández Fernández, Xusto and Monserrat, Lorenzo and Mogollón, Maria Victoria and Ripoll, Tomás and Richard, Pascale and Palomino Doza, Julian and Fontalba, Ana and Alonso-Pulpón, Luis and Cobo-Marcos, Marta and Gómez-Bueno, Manuel and González-López, Esther and Hernández-Hernández, Aitor and Hernández-Pérez, Francisco José and López-Sainz, Ángela and Restrepo-Córdoba, Alejandra and Segovia-Cubero, Javier and Rosa Longobardo, Félix and Limeres, Javier and López-Garrido, Miguel A and Jiménez-Jaimez, Juan and Rangel Sousa, Diego and Peña, Maria Luisa and Morris-Hey, Thomas and Cook, Stuart A and Midwinter, William and Roberts, Angharad M and Ware, James S and Walsh, Roddy and Rocha-Lopes, Luis and Savvatis, Konstantinos and Syrris, Petros and Michalak, Ewa and Ploski, Rafal and Sobieszczanska-Malek, Malgorzata and Baas, Annette and Dooijes, Dennis and European Genetic Cardiomyopathies and European Genetic Cardiomyopathies Initiative Investigators
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2471 - 2481
The (BLC2-associated athanogene 3) gene codes for an antiapoptotic protein located on the sarcomere Z-disc. Mutations in are associated with dilated... 
genetics | BAG3 | prognosis | dilated cardiomyopathy | CARDIAC & CARDIOVASCULAR SYSTEMS | GENETIC ISSUES | VARIANTS | HEART-FAILURE | AUTOPHAGY | ASSOCIATION | Cardiomyopathy, Dilated - genetics | Follow-Up Studies | Humans | Middle Aged | Heart Failure - genetics | Male | Mutation - genetics | Electrocardiography - statistics & numerical data | Young Adult | Cardiomyopathy, Dilated - physiopathology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Apoptosis Regulatory Proteins - genetics | Adult | Cardiomyopathy, Dilated - diagnosis | Female | Heart Failure - diagnosis | Cohort Studies | Analysis | Genetic aspects | Cardiomyopathy, Dilated | Immunohistochemistry | Heart | Arrhythmia | Syngeneic grafts | Cardiomyopathy | Genomics | Genes | Sex | Cardiovascular disease | Transplantation | Males | Kinases | Proteins | Ultrasonic imaging | Sinuses | Electrocardiography | Localization | Heart diseases | Relocation | Age | Deoxyribonucleic acid--DNA | Evaluation | Phenotypes | Statistical analysis | Heart transplantation | Patients | Dilated cardiomyopathy | Mutation | Ventricle | Ejection | BAG3, BCL2-associated athanogene 3 | LVEF, left ventricular ejection fraction | SCD, sudden cardiac death | DCM, dilated cardiomyopathy | ICD, implantable cardioverter-defibrillator | IQR, interquartile range | VF, ventricular fibrillation | SVT, sustained ventricular tachycardia | LVAD, left ventricular assist device | LVEDD, left ventricular end-diastolic diameter | HTx, heart transplantation | HF, heart failure | ECG, electrocardiogram | NYHA, New York Heart Association
Journal Article
Insights into Imaging, ISSN 1869-4101, 10/2018, Volume 9, Issue 5, pp. 695 - 707
Journal Article
Stem Cell Reports, ISSN 2213-6711, 11/2018, Volume 11, Issue 5, pp. 1226 - 1243
Hypertrophic cardiomyopathy (HCM) is a primary disorder of contractility in heart muscle. To gain mechanistic insight and guide pharmacological rescue, this... 
contractile function | cardiomyopathy | hypertrophy | arrhythmia
Journal Article