Novel Filamin C missense mutation associated with severe restrictive cardiomyopathy overlapping with left ventricular non-compaction
Garcia Hernandez, S, Ortiz-Genga, M, Analia Ramos, K, Ochoa, J.P, Lamounier, A, Fernandez, X, Cardenas, I, Garcia-Giustiniani, D, Brogger, M.N, Cicerchia, M.N, Fernandez, G, Monserrat, L
Published in European heart journal (01.11.2020)
Published in European heart journal (01.11.2020)
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Narrowing of the neonatal region in the FBN1 gene
Brogger, M N, Fernandez Ferro, G, Cardenas Reyes, I, Ochoa, J P, Garcia Hernandez, S, Valverde, M, Fernandez, X, Garcia Giustiniani, D, Lamounier, A, De La Higuera Romero, L, Ortiz Genga, M, Monserrat, L, McKenna, W J
Published in European heart journal (12.10.2021)
Published in European heart journal (12.10.2021)
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Journal Article
Genetic variants as determinants of outcome in lamin A/C-related cardiac disease
Garcia Hernandez, S, Ortiz-Genga, M, Ochoa, J P, Lamounier, A, Fernandez, X, Cardenas, I, Garcia-Giustiniani, D, Brogger, M N, Fernandez, G, Valverde, M, Monserrat, L, McKenna, W J
Published in European heart journal (12.10.2021)
Published in European heart journal (12.10.2021)
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Marfan syndrome: genetic variant determinants of cardiovascular outcomes
Brogger, M N, Fernandez Ferro, G, Cardenas Reyes, I, Ochoa, J P, Garcia Hernandez, S, Fernandez, X, Garcia Giustiniani, D, Lamounier, A, Valverde, M, De La Higuera Romero, L, Ortiz Genga, M, Monserrat, L, McKenna, W J
Published in European heart journal (12.10.2021)
Published in European heart journal (12.10.2021)
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4381Prognostic implications of pathogenic truncating variants in the TTN gene
Cicerchia, M N, Pena Pena, M L, Salazar Mendiguchia, J, Ochoa, J, Lamounier Junior, A, Trujillo, J P, Palomino Doza, J, Cardenar Reyes, I, Garcia Giustiniani, D, Fernandez Fernandez, X, Barraza Garcia, J, Rodriguez Garrido, J, Barriales Villa, R, Ortiz-Genga, M, Monserrat Iglesias, L
Published in European heart journal (01.08.2018)
Published in European heart journal (01.08.2018)
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Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
Lopes, Luis R, Losi, Maria-Angela, Sheikh, Nabeel, Laroche, Cécile, Charron, Philippe, Gimeno, Juan, Kaski, Juan P, Maggioni, Aldo P, Tavazzi, Luigi, Arbustini, Eloisa, Brito, Dulce, Celutkiene, Jelena, Hagege, Albert, Linhart, Ales, Mogensen, Jens, Garcia-Pinilla, José Manuel, Ripoll-Vera, Tomas, Seggewiss, Hubert, Villacorta, Eduardo, Caforio, Alida, Elliott, Perry M
Published in European heart journal. Quality of care & clinical outcomes (01.01.2023)
Published in European heart journal. Quality of care & clinical outcomes (01.01.2023)
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602Sudden death risk in carriers of KCNH2 mutations. Influence of gender, location and type of mutation
Garcia-Giustiniani, DA, Ochoa, JP, Ortiz-Genga, M., Barriales-Villa, R., Salazar-Mendiguchia, J., Cicerchia, M., Lamounier Junior, A., Rodriguez-Garrido, J., Barraza-Garcia, J., Cardenas-Reyes, I., Fernandez-Fernandez, X., Trujillo-Quintero, JP, Monserrat, L.
Published in Europace (London, England) (01.06.2017)
Published in Europace (London, England) (01.06.2017)
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Utilidad del diagnóstico genético en la miocardiopatía hipertrófica de una mujer que desea ser madre: la información es clave
Barriales-Villa, Roberto, García-Giustiniani, Diego A, Ortiz-Genga, Martin, Monserrat, Lorenzo
Published in Revista española de cardiologia (01.04.2014)
Published in Revista española de cardiologia (01.04.2014)
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