Search Results - "Luengos, David Crémer"

New Variant in Placophilin-2 Gene Causing Arrhythmogenic Myocardiopathy by Caimi-Martinez, Fiama, Antoniutti, Guido, Blanco, Rocio, García de la Villa, Bernardo, Alvarenga, Nelson, Govea-Callizo, Nancy, Torres-Juan, Laura, Heine-Suñer, Damián, Rosell-Andreo, Jordi, Luengos, David Crémer, Alvarez-Rubio, Jorge, Ripoll-Vera, Tomás

“…Arrhythmogenic cardiomyopathy (ACM) is an inherited disease characterized by progressive fibroadipose replacement of cardiomyocytes. Its diagnosis is based on…”
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The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans by Ripoll Vera, Tomás, Monserrat Iglesias, Lorenzo, Hermida Prieto, Manuel, Ortiz, Martin, Rodriguez Garcia, Isabel, Govea Callizo, Nancy, Gómez Navarro, Carlos, Rosell Andreo, Jordi, Gámez Martínez, José María, Pons Lladó, Guillermo, Cremer Luengos, David, Torres Marqués, Joan

“…Abstract Background The R820W mutation in the MYBPC3 gene has been associated with the development of hypertrophic cardiomyopathy (HCM) in rag-doll cats, but…”
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Natural History of MYH7-Related Dilated Cardiomyopathy by de Frutos, Fernando, Ochoa, Juan Pablo, Navarro-Peñalver, Marina, Baas, Annette, Bjerre, Jesper Vandborg, Zorio, Esther, Méndez, Irene, Lorca, Rebeca, Verdonschot, Job A.J., García-Granja, Pablo Elpidio, Bilinska, Zofia, Fatkin, Diane, Fuentes-Cañamero, M. Eugenia, García-Pinilla, José M., 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., Restrepo-Córdoba, María Alejandra, Palomino-Doza, Julián, Ruiz-Guerrero, Luis, Sarquella-Brugada, Georgia, Perez-Perez, Alberto José, Bermúdez-Jiménez, Francisco José, Ripoll-Vera, Tomas, Rasmussen, Torsten Bloch, Jansen, Mark, Sabater-Molina, Maria, Elliot, Perry M., Garcia-Pavia, Pablo, Cabrera-Romero, Eva, Cobo-Marcos, Marta, Escobar-Lopez, Luis, Domínguez, Fernando, González-López, Esther, Gimeno-Blanes, Juan Ramón, Dooijes, Dennis, López Ledesma, Bernabé, Roche Fortea, Inés, Bermejo, Javier, Espinosa, Maria Angeles, Fernández, Ana Isabel, Vilches, Silvia, Gómez, Cristina, Gómez, Juan, Coto, Eliecer, Rodríguez Reguero, José Julián, Heymans, S.R.B., Brunner, H.G., López-Díaz, Javier, Truszkowska, Grażyna, Ploski, Rafal, Chmielewski, Przemysław, Johnson, Renee, Robles-Mezcua, Ainhoa, Díaz-Expósito, Arancha, Pérez-Cabeza, Alejandro I., Jiménez-Rubio, Clara, Payá, Vicente Climent, Favilli, Silvia, Syrris, Petros, Cannie, Douglas, Billon, Clarisse, Lopez-Sainz, Angela, Calvo, Margarita, Fernández de Bobadilla, Ángela Cacicedo, Onaindia-Gandarias, Jose Juan, Gaztañaga-Arantzamendi, Larraitz, Zamarreño-Golvano, Estibaliz, Limeres, Javier, Gutiérrez-García, Laura, Villacorta, Eduardo, Haas, Jan, Krebsova, Alice, Mogensen, Jens, Cesar, Sergi, Campuzano, Oscar, Gutiérrez, Raúl Franco, Alvarez-Rubio, Jorge, Cremer-Luengos, David, Antoniutti, Guido, Caimi-Martinez, Fiama, Macías, Rosa, Jiménez-Jáimez, Juan, Peña-Peña, María Luisa, Díez-Aja López, Salvador Lucas, Acereda, Tania Pino, Corada, Blanca Arnáez, Piqueras-Flores, Jesús, Negreira-Caamaño, Martin

“…BACKGROUNDVariants in myosin heavy chain 7 (MYH7) are responsible for disease in 1% to 5% of patients with dilated cardiomyopathy (DCM); however, the clinical…”
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The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans by Ripoll Vera, Tomás, Monserrat Iglesias, Lorenzo, Hermida Prieto, Manuel, Ortiz, Martin, Rodriguez Garcia, Isabel, Govea Callizo, Nancy, Gómez Navarro, Carlos, Rosell Andreo, Jordi, Gámez Martínez, José María, Pons Lladó, Guillermo, Cremer Luengos, David, Torres Marqués, Joan

“…BACKGROUNDThe R820W mutation in the MYBPC3 gene has been associated with the development of hypertrophic cardiomyopathy (HCM) in rag-doll cats, but had not…”
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