Zobrazeno 1 - 10
of 57
pro vyhledávání: '"M. Ortiz Genga"'
Autor:
A Trancuccio, A Mazzanti, D Kukavica, G Giannini, M Memmi, P Gambelli, R Bloise, M Marino, M Morini, M Ortiz-Genga, C Napolitano, S G Priori
Publikováno v:
European Heart Journal. 43
Background Recently, a novel genetic-based classification for Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) has been proposed to distinguish “typical” (RYR2 and CASQ2 genes) and “atypical” (TRDN, TECRL, CALM1–3, RYR2 loss-of-
Autor:
D Kukavica, A Mazzanti, A Trancuccio, G Giannini, M Marino, M Memmi, P Gambelli, R Bloise, M Morini, M Ortiz-Genga, C Napolitano, S G Priori
Publikováno v:
European Heart Journal. 43
Background Due to the catecholaminergic nature of arrhythmias that define the Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), beta-blockers (BBs) represent the first line therapy for this severe arrhythmogenic syndrome. Despite optimal
Autor:
S Garcia Hernandez, L De La Higuera Romero, X Fernandez, M Valverde Gomez, L Cazon Varela, R Peteiro Deben, P Rebolo, A Sanluis Verdes, I Cardenas, M Ortiz-Genga, A Amor Salamanca, M Perez Barbeito, I Gomez Diaz, M Sanchez Flores, J P Ochoa
Publikováno v:
European Heart Journal. 43
Introduction MYH7 encodes to β-cardiac myosin heavy chain, a large and pleomorphic protein, conformed by different and well-functionally characterized domains. This gene has an enormous contribution to hypertrophic cardiomyopathy (HCM) but also to o
Autor:
Lorenzo Monserrat, S Garcia Hernandez, G Fernandez Ferro, Xusto Fernández, M N Brogger, William J. McKenna, D Garcia Giustiniani, L De La Higuera Romero, I Cardenas Reyes, A Lamounier, M. Ortiz Genga, Juan Pablo Ochoa, M Valverde
Publikováno v:
European Heart Journal. 42
Background Neonatal Marfan syndrome (MFS) is considered the most severe form of MFS and is characterized by early childhood death due to congestive heart failure. It has been suggested that genetic variants associated with this clinical presentation,
Autor:
Lorenzo Monserrat, M Valverde, M. Ortiz Genga, I Cardenas Reyes, Xusto Fernández, D Garcia Giustiniani, M N Brogger, William J. McKenna, G Fernandez Ferro, S Garcia Hernandez, L De La Higuera Romero, Juan Pablo Ochoa, A Lamounier
Publikováno v:
European Heart Journal. 42
Background Marfan syndrome is a systemic connective tissue disorder caused by genetic variants in the fibrillin-1 (FBN1) gene. Cardiovascular complications are the leading cause of mortality. Purpose To compare cardiovascular outcome by gender and by
Akademický článek
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Autor:
J. Rodriguez Garrido, Douglas Garcia, Marcos Cicerchia, A. Lamounier Junior, M. Ortiz Genga, Juan Pablo Ochoa, J. Salazar Mendiguchia, L. Monserrat Iglesias, I Cardenas Reyes
Publikováno v:
European Heart Journal. 38
Autor:
J. Salazar Mendiguchia, L. Monserrat Iglesias, Douglas Garcia, A. Lamounier Junior, Marcos Cicerchia, M. Ortiz Genga, Juan Pablo Ochoa, J. Rodriguez Garrido, I Cardenas Reyes
Publikováno v:
European Heart Journal. 38
Autor:
A. Lamounier Junior, Joel Salazar-Mendiguchía, J. Rodriguez-Garrido, Lorenzo Monserrat, M. Ortiz-Genga, Da. Garcia-Giustiniani, Marcos Cicerchia, X. Fernandez-Fernandez, Jp. Trujillo-Quintero, J. Barraza-Garcia, I. Cardenas-Reyes, Roberto Barriales-Villa, Jp. Ochoa
Publikováno v:
EP Europace. 19:iii126-iii127
Akademický článek
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