Search Results - "Brögger, Maria Noël"

Association of Genetic Variants With Outcomes in Patients With Nonischemic Dilated Cardiomyopathy by Escobar-Lopez, Luis, Ochoa, Juan Pablo, Mirelis, Jesús G., Espinosa, María Ángeles, Navarro, Marina, Gallego-Delgado, María, Barriales-Villa, Roberto, Robles-Mezcua, Ainhoa, Basurte-Elorz, María Teresa, Gutiérrez García-Moreno, Laura, Climent, Vicente, Jiménez-Jaimez, Juan, Mogollón-Jiménez, María Victoria, Lopez, Javier, Peña-Peña, María Luisa, García-Álvarez, Ana, Brion, María, Ripoll-Vera, Tomas, Palomino-Doza, Julián, Tirón, Coloma, Idiazabal, Uxua, Brögger, Maria Noël, García-Hernández, Soledad, Restrepo-Córdoba, María Alejandra, Gonzalez-Lopez, Esther, Méndez, Irene, Sabater, María, Villacorta, Eduardo, Larrañaga-Moreira, José M., Abecia, Ana, Fernández, Ana Isabel, García-Pinilla, José M., Rodríguez-Palomares, José F., Gimeno-Blanes, Juan Ramón, Bayes-Genis, Antoni, Lara-Pezzi, Enrique, Domínguez, Fernando, Garcia-Pavia, Pablo

“…The clinical relevance of genetic variants in nonischemic dilated cardiomyopathy (DCM) is unsettled. The study sought to assess the prognostic impact of…”
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Correlación genotipo-fenotipo en miocardiopatía hipertrófica: un estudio multicéntrico en Portugal y España sobre la variante p.Arg21Leu de TPM1 by Lamounier Junior, Arsonval, Guitián González, Alba, Rodríguez Vilela, Alejandro, Repáraz Andrade, Alfredo, Rubio Alcaide, Álvaro, Berta Sousa, Ana, Benito López, Carmen, Alonso García, Diego, Fernández Ferro, Germán, Cruz, Inês, Cárdenas Reyes, Ivonne Johana, Salazar-Mendiguchía García, Joel, Larrañaga-Moreira, José María, Ochoa, Juan Pablo, Palomino-Doza, Julián, de la Higuera Romero, Luis, Nicolás Cicerchia, Marcos, Restrepo Córdoba, María Alejandra, Peña-Peña, María Luisa, Noël Brögger, Maria, Loureiro, Marilia, Mogollón Jiménez, María Victoria, Bilbao Quesada, Raquel, Franco Gutiérrez, Raúl, García Hernández, Soledad, Ripoll-Vera, Tomás, Fernández, Xusto, Azevedo, Olga, García Pavía, Pablo, Lopes, Luis R., Ortiz, Martín, Brito, Dulce, Barriales-Villa, Roberto, Monserrat Iglesias, Lorenzo

“…TPM1 es uno de los principales genes en la miocardiopatía hipertrófica (MCH). La información clínica sobre portadores es relativamente escasa, lo cual limita…”
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Small‐molecule inhibition of MuRF1 attenuates skeletal muscle atrophy and dysfunction in cardiac cachexia by Bowen, Thomas Scott, Adams, Volker, Werner, Sarah, Fischer, Tina, Vinke, Paulien, Brogger, Maria Noel, Mangner, Norman, Linke, Axel, Sehr, Peter, Lewis, Joe, Labeit, Dittmar, Gasch, Alexander, Labeit, Siegfried

“…Background Muscle ring finger 1 (MuRF1) is a muscle‐specific ubiquitin E3 ligase activated during clinical conditions associated with skeletal muscle wasting…”
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Genotype-phenotype correlations in hypertrophic cardiomyopathy: a multicenter study in Portugal and Spain of the TPM1 p.Arg21Leu variant by Lamounier Junior, Arsonval, Guitián González, Alba, Rodríguez Vilela, Alejandro, Repáraz Andrade, Alfredo, Rubio Alcaide, Álvaro, Berta Sousa, Ana, Benito López, Carmen, Alonso García, Diego, Fernández Ferro, Germán, Cruz, Inês, Cárdenas Reyes, Ivonne Johana, Salazar-Mendiguchía García, Joel, Larrañaga-Moreira, José María, Ochoa, Juan Pablo, Palomino-Doza, Julián, de la Higuera Romero, Luis, Nicolás Cicerchia, Marcos, Restrepo Córdoba, María Alejandra, Peña-Peña, María Luisa, Noël Brögger, Maria, Loureiro, Marilia, Mogollón Jiménez, María Victoria, Bilbao Quesada, Raquel, Franco Gutiérrez, Raúl, García Hernández, Soledad, Ripoll-Vera, Tomás, Fernández, Xusto, Azevedo, Olga, García Pavía, Pablo, Lopes, Luis R., Ortiz, Martín, Brito, Dulce, Barriales-Villa, Roberto, Monserrat Iglesias, Lorenzo

“…TPM1 is one of the main hypertrophic cardiomyopathy (HCM) genes. Clinical information on carriers is relatively scarce, limiting the interpretation of genetic…”
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