Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Martín Ortiz-Genga"'
Autor:
Arthur A. M. Wilde, Christopher Semsarian, Manlio F. Márquez, Alireza Sepehri Shamloo, Michael J. Ackerman, Euan A. Ashley, Back Sternick Eduardo, Héctor Barajas‐Martinez, Elijah R. Behr, Connie R. Bezzina, Jeroen Breckpot, Philippe Charron, Priya Chockalingam, Lia Crotti, Michael H. Gollob, Steven Lubitz, Naomasa Makita, Seiko Ohno, Martín Ortiz‐Genga, Luciana Sacilotto, Eric Schulze‐Bahr, Wataru Shimizu, Nona Sotoodehnia, Rafik Tadros, James S. Ware, David S. Winlaw, Elizabeth S. Kaufman, Takeshi Aiba, Andreas Bollmann, Jong‐Il Choi, Aarti Dalal, Francisco Darrieux, John Giudicessi, Mariana Guerchicoff, Kui Hong, Andrew D. Krahn, Ciorsti Mac Intyre, Judith A. Mackall, Lluís Mont, Carlo Napolitano, Pablo Ochoa Juan, Petr Peichl, Alexandre C. Pereira, Peter J. Schwartz, Jon Skinner, Christoph Stellbrink, Jacob Tfelt‐Hansen, Thomas Deneke
Publikováno v:
Journal of Arrhythmia, Vol 38, Iss 4, Pp 491-553 (2022)
Externí odkaz:
https://doaj.org/article/065b869d10df4d35a27b0f57e20fcc2b
Autor:
Juan Jiménez-Jáimez, Julián Palomino Doza, Ángeles Ortega, Rosa Macías-Ruiz, Francesca Perin, M Mar Rodríguez-Vázquez del Rey, Martín Ortiz-Genga, Lorenzo Monserrat, Roberto Barriales-Villa, Enrique Blanca, Miguel Álvarez, Luis Tercedor
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0153851 (2016)
BACKGROUND:Calmodulin 1, 2 and 3 (CALM) mutations have been found to cause cardiac arrest in children at a very early age. The underlying aetiology described is long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia (CPVT) and
Externí odkaz:
https://doaj.org/article/2ecdb7b638fd48dfa1da43b2c33b288c
Autor:
Arthur A. M. Wilde, Christopher Semsarian, Manlio F. Márquez, Alireza Sepehri Shamloo, Michael J. Ackerman, Euan A. Ashley, Back Sternick Eduardo, Héctor Barajas‐Martinez, Elijah R. Behr, Connie R. Bezzina, Jeroen Breckpot, Philippe Charron, Priya Chockalingam, Lia Crotti, Michael H. Gollob, Steven Lubitz, Naomasa Makita, Seiko Ohno, Martín Ortiz‐Genga, Luciana Sacilotto, Eric Schulze‐Bahr, Wataru Shimizu, Nona Sotoodehnia, Rafik Tadros, James S. Ware, David S. Winlaw, Elizabeth S. Kaufman, Takeshi Aiba, Andreas Bollmann, Jong‐Il Choi, Aarti Dalal, Francisco Darrieux, John Giudicessi, Mariana Guerchicoff, Kui Hong, Andrew D. Krahn, Ciorsti Mac Intyre, Judith A. Mackall, Lluís Mont, Carlo Napolitano, Pablo Ochoa Juan, Petr Peichl, Alexandre C. Pereira, Peter J. Schwartz, Jon Skinner, Christoph Stellbrink, Jacob Tfelt‐Hansen, Thomas Deneke
Publikováno v:
Journal of Arrhythmia. 38:491-553
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abce9b25652c5ad7a487a7edfb966f8e
https://doi.org/10.1002/joa3.12717
https://doi.org/10.1002/joa3.12717
Autor:
Joel, Salazar-Mendiguchía, Juan Pablo, Ochoa, Julian, Palomino-Doza, Fernando, Domínguez, Carles, Díez-López, Mohammed, Akhtar, Soraya, Ramiro-León, María M, Clemente, Antonia, Pérez-Cejas, María, Robledo, Iria, Gómez-Díaz, María Luisa, Peña-Peña, Vicente, Climent, Francisco, Salmerón-Martínez, Celestino, Hernández, Pablo E, García-Granja, M Victoria, Mogollón, Ivonne, Cárdenas-Reyes, Marcos, Cicerchia, Diego, García-Giustiniani, Arsonval, Lamounier, Belén, Gil-Fournier, Felícitas, Díaz-Flores, Rafael, Salguero, Luis, Santomé, Petros, Syrris, Montse, Olivé, Pablo, García-Pavía, Martín, Ortiz-Genga, Perry M, Elliott, Lorenzo, Monserrat, Juan Pablo, Trujillo-Quintero
Publikováno v:
Heart
Objective Up to 50% of patients with hypertrophic cardiomyopathy (HCM) show no disease-causing variants in genetic studies. TRIM63 has been suggested as a candidate gene for the development of cardiomyopathies, although evidence for a causative role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c8a508c2449acab35307ea7a3fbb05a
https://pubmed.ncbi.nlm.nih.gov/32451364
https://pubmed.ncbi.nlm.nih.gov/32451364
Autor:
Lorenzo Monserrat, Andrea Mazzanti, Martin Ortiz-Genga, Roberto Barriales-Villa, Diego Garcia-Giustiniani, Juan Ramon Gimeno-Blanes
Publikováno v:
Cardiogenetics, Vol 1, Iss 1, Pp e8-e8 (2011)
The inherited cardiovascular diseases, including cardiomyopathies, channelopaties and inherited diseases of the aorta are heterogeneous conditions with highly variable morphologic and functional features, clinical presentation, evolution and prognosi
Externí odkaz:
https://doaj.org/article/cb7e7193b3994493924c9e23d121a5ee