Zobrazeno 1 - 10 of 28 pro vyhledávání: '"José M Larrañaga-Moreira"'
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Akademický článek
Hypokinetic hypertrophic cardiomyopathy: clinical phenotype, genetics, and prognosis
Autor: Yishay Wasserstrum, José M. Larrañaga‐Moreira, Cristina Martinez‐Veira, Edward Itelman, Dor Lotan, Avi Sabbag, Rafael Kuperstein, Yael Peled, Dov Freimark, Roberto Barriales‐Villa, Michael Arad
Publikováno v: ESC Heart Failure, Vol 9, Iss 4, Pp 2301-2312 (2022)
Abstract Aims To describe the phenotype, genetics, and events associated with the development of hypertrophic cardiomyopathy (HCM) with reduced ventricular function (HCMr). Heart failure in HCM is usually associated with preserved ejection fraction,
Externí odkaz: https://doaj.org/article/6ea0465872dc4b94a3bdb7982da44eb4
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3
Clinical Risk Prediction in Patients With Left Ventricular Myocardial Noncompaction
Autor: Josep Ramon Marsal, Laura Gutierrez-Garcia, Juan Ramón Gimeno-Blanes, Pier Giorgio Masci, Juan Jiménez-Jáimez, Gisela Teixido-Tura, Marta Codina-Solà, Gerard Oristrell, Coloma Tiron, Ignacio Ferreira-González, Andrea Guala, Pablo García-Pavía, Paula Fernández-Álvarez, Juan José Santos-Mateo, Esther Zorio, José Luis de la Pompa, Artur Evangelista, José Manuel García-Pinilla, Daniele Andreini, Eduardo Villacorta, Tomás Ripoll-Vera, Ángela López-Sainz, José Rodríguez-Palomares, José Antonio Sorolla-Romero, Gianluca Pontone, Lucia La Mura, Javier Limeres, Jan Bogaert, Mar Borregan, Augusto Sao Avilés, Julián Palomino-Doza, Rafaela Soler-Fernandez, Aida Ribera, Josefa González-Carrillo, José M. Larrañaga-Moreira, Guillem Casas, Giovanni Donato Aquaro, Roberto Barriales-Villa, Antoni Bayes-Genis
Publikováno v: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
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Left ventricular noncompaction (LVNC) is a heterogeneous entity with uncertain prognosis. This study sought to develop and validate a prediction model of major adverse cardiovascular events (MACE) and to identify LVNC cases without events during long
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14e8a730451c9b72a9f4bb3b686d9ef1
https://doi.org/10.1016/j.jacc.2021.06.016
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4
Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy
Autor: Ruxandra Jurcut, Andrea Ros, Luisa Politano, Juan Jiménez-Jáimez, Pablo García-Pavía, Ali Yilmaz, Job A J Verdonschot, Alberto Palladino, María I. García-Álvarez, Luis Ruiz-Guerrero, Karim Wahbi, Ana García-Álvarez, Luis R. Lopes, Michael Arad, Maria Teresa Basurte Elorz, Jens Mogensen, Roberto Barriales-Villa, Paloma Jordà, José M. Larrañaga-Moreira, Francisco Bermúdez-Jiménez, Zofia T. Bilińska, Benjamin Meder, Rosa L. E. van Loon, Zornitsa Shomanova, Tanya Stojkovic, Francesca Girolami, Miloš Kubánek, Julián Palomino-Doza, Perry M. Elliott, Torsten Bloch Rasmussen, Dov Freimark, Maria Robledo Iñarritu, María Alejandra Restrepo-Córdoba, Giovanni Quarta, Pascal Laforêt, Anca Florian, Juan Pablo Ochoa, Regina Pribe-Wolferts, Ramon Brugada, Rasmus B Hansen, Vicente Climent-Payá, Fernando Domínguez, José Rodríguez-Palomares
Publikováno v: European journal of heart failure, 23(8), 1276-1286. Wiley
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Restrepo-Cordoba, M A, Wahbi, K, Florian, A R, Jiménez-Jáimez, J, Politano, L, Arad, M, Climent-Paya, V, Garcia-Alvarez, A, Hansen, R B, Larrañaga-Moreira, J M, Kubanek, M, Lopes, L R, Ros, A, Jurcut, R, Rasmussen, T B, Ruiz-Guerrero, L, Pribe-Wolferts, R, Palomino-Doza, J, Bilinska, Z, Rodríguez-Palomares, J F, Van Loon, R L E, Basurte Elorz, M T, Quarta, G, Robledo Iñarritu, M, Verdonschot, J A J, Stojkovic, T, Shomanova, Z, Bermudez-Jimenez, F, Palladino, A, Freimark, D, García-Álvarez, M I, Jorda, P, Dominguez, F, Ochoa, J P, Girolami, F, Brugada, R, Meder, B, Barriales-Villa, R, Mogensen, J, Laforêt, P, Yilmaz, A, Elliott, P, Garcia-Pavia, P & for the European Genetic Cardiomyopathies Initiative Investigators (see online supplementary Appendix S1) 2021, ' Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy ', European Journal of Heart Failure, vol. 23, no. 8, pp. 1276-1286 . https://doi.org/10.1002/ejhf.2250
Aims: Dilated cardiomyopathy (DCM) associated with dystrophin gene (DMD) mutations in individuals with mild or absent skeletal myopathy is often indistinguishable from other DCM forms. We sought to describe the phenotype and prognosis of DMD associat
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1780331ac79e5fb7857261abd885ef77
https://doi.org/10.1002/ejhf.2250
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5
Efecto de la edad y el sexo en el rendimiento diagnóstico del ecocardiograma en pacientes con síncope
Autor: F.J. Broullón-Molanes, Nemesio Álvarez-García, José M. Larrañaga-Moreira, Cayetana Barbeito-Caamaño, Alberto Bouzas-Mosquera, J M Vazquez-Rodriguez
Publikováno v: Revista Clínica Española. 221:217-220
Resumen Introduccion El sincope es motivo de numerosas pruebas diagnosticas, entre las que esta el ecocardiograma transtoracico (ETT). Existe evidencia previa que sugiere escasa utilidad de esta prueba. Nuestro objetivo fue evaluar su rendimiento dia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7b87e671baed656212342c32e7a28cc8
https://doi.org/10.1016/j.rce.2019.05.017
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8
Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator
Autor: Alexandros Protonotarios, Riccardo Bariani, Chiara Cappelletto, Menelaos Pavlou, Alba García-García, Alberto Cipriani, Ioannis Protonotarios, Adrian Rivas, Regitze Wittenberg, Maddalena Graziosi, Zafeirenia Xylouri, José M Larrañaga-Moreira, Antonio de Luca, Rudy Celeghin, Kalliopi Pilichou, Athanasios Bakalakos, Luis Rocha Lopes, Konstantinos Savvatis, Davide Stolfo, Matteo Dal Ferro, Marco Merlo, Cristina Basso, Javier Limeres Freire, Jose F Rodriguez-Palomares, Toru Kubo, Tomas Ripoll-Vera, Roberto Barriales-Villa, Loizos Antoniades, Jens Mogensen, Pablo Garcia-Pavia, Karim Wahbi, Elena Biagini, Aris Anastasakis, Adalena Tsatsopoulou, Esther Zorio, Juan R Gimeno, Jose Manuel Garcia-Pinilla, Petros Syrris, Gianfranco Sinagra, Barbara Bauce, Perry M Elliott
Publikováno v: Protonotarios, A, Bariani, R, Cappelletto, C, Pavlou, M, García-García, A, Cipriani, A, Protonotarios, I, Rivas, A, Wittenberg, R, Graziosi, M, Xylouri, Z, Larrañaga-Moreira, J M, de Luca, A, Celeghin, R, Pilichou, K, Bakalakos, A, Lopes, L R, Savvatis, K, Stolfo, D, Dal Ferro, M, Merlo, M, Basso, C, Freire, J L, Rodriguez-Palomares, J F, Kubo, T, Ripoll-Vera, T, Barriales-Villa, R, Antoniades, L, Mogensen, J, Garcia-Pavia, P, Wahbi, K, Biagini, E, Anastasakis, A, Tsatsopoulou, A, Zorio, E, Gimeno, J R, Garcia-Pinilla, J M, Syrris, P, Sinagra, G, Bauce, B & Elliott, P M 2022, ' Importance of genotype for risk stratification in arrhythmogenic right ventricular cardiomyopathy using the 2019 ARVC risk calculator ', European Heart Journal, vol. 43, no. 32, ehac235, pp. 3053-3067 . https://doi.org/10.1093/eurheartj/ehac235
EUROPEAN HEART JOURNAL
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
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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 diagnosis of ARVC and no history of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0a27b0764d2ef79fd613554a9abda01
http://hdl.handle.net/11577/3452053
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9
Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy
Autor: Laura Gutiérrez García-Moreno, Luis Escobar-Lopez, María Gallego-Delgado, Maria Victoria Mogollón-Jimenez, María Ángeles Espinosa, Juan Pablo Ochoa, M N Brogger, Jesús G. Mirelis, Pablo García-Pavía, Juan Ramón Gimeno-Blanes, Juan Jiménez-Jáimez, Irene Méndez, María Alejandra Restrepo-Córdoba, Julián Palomino-Doza, Ana I. Fernández, José Manuel García-Pinilla, María Brion, Tomás Ripoll-Vera, Roberto Barriales-Villa, Vicente Climent, Marina Navarro, María Luisa Peña-Peña, Uxua Idiazabal, Esther Gonzalez-Lopez, Ana García-Álvarez, Ana Abecia, Eduardo Villacorta, Antoni Bayes-Genis, J F Rodriguez-Palomares, Ainhoa Robles-Mezcua, José M. Larrañaga-Moreira, Javier Lopez, Coloma Tiron, María Teresa Basurte-Elorz, María Sabater, Enrique Lara-Pezzi, Fernando Dominguez, Soledad García-Hernández
Publikováno v: JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
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Journal Of The American College Of Cardiology
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
BACKGROUND The clinical relevance of genetic variants in nonischemic dilated cardiomyopathy (DCM) is unsettled. OBJECTIVES The study sought to assess the prognostic impact of disease-causing genetic variants in DCM. METHODS Baseline and longitudinal
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e32b9883b7a20b936392fa1d01f0a2b
https://pubmed.ncbi.nlm.nih.gov/35115108
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