Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elsa Silva-Oropeza"'
Autor:
Enrique Velázquez-Rodríguez, Norberto García-Hernández, Elsa Silva-Oropeza, Santiago Jiménez-Arteaga, Arturo Martínez-Sánchez, Carlos Alva-Espinoza, Felipe David-Gómez, Lucelli Yáñez-Gutiérrez
Publikováno v:
Boletín Médico del Hospital Infantil de México, Vol 79, Iss 4 (2022)
Background: Idiopathic ventricular tachycardia (VT) in children with structurally normal hearts is generally unrelated to the risk of sudden arrhythmic death. Still, it may be associated with deterioration in the quality of life. VT involving the fas
Externí odkaz:
https://doaj.org/article/d982edb34b5d4a75b16955582ab3e155
Autor:
Elsa Silva-Oropeza, Esperanza García Reyes, Lydia Rodríguez Hernández, Luisa Beirana Palencia
Publikováno v:
Arquivos Brasileiros de Cardiologia, Vol 82, Iss 5, Pp 487-489 (2004)
Externí odkaz:
https://doaj.org/article/11dd260292b94a83878b25ecd3b4e90c
Autor:
Jorge Marin, Claudio Muratore, Nicolás Reyes, Rafael Rabinovich, Jorge Gonzalez-Zuelgaray, Brett J. Peterson, José Luis Martínez Ramos, Maria Cristina Tentori, Rubén Aguayo, Elsa Silva Oropeza, Oscar Pellizon
Publikováno v:
EP Europace. 15:236-242
Aims This cross-sectional study evaluated the application of accepted international implantable cardioverter defibrillator (ICD) guidelines for primary prevention of sudden cardiac death in patients with heart failure. Methods and results The PLASMA
Autor:
Francisco Martínez Baca-López, Enrique Bernal-Ruiz, Elsa Silva-Oropeza, Ana Lilia Rayas-Gómez, Lucelli Yánez-Gutiérrez, Erick Ramírez-Arias, Rosa Marisol Alonso Bravo
Publikováno v:
Echocardiography. 22:517-524
Three cases of patients with hypertropic cardiomyopathy, apical aneurysm, and mid-ventricular obstruction are presented. Two patients were diagnosed first by two-dimensional and Doppler echocardiography, which showed mid-ventricular obliteration, cha
Autor:
Elsa, Silva-Oropeza, Esperanza, García Reyes, Lydia, Rodríguez Hernández, Luisa, Beirana Palencia
Publikováno v:
Arquivos brasileiros de cardiologia. 82(5)
Publikováno v:
American heart journal. 145(2)
Background Familial dilated cardiomyopathy (FDCM) is attributed to defects in cytoskeletal proteins, and different patterns of inheritance and phenotypic expressions according to assorted-protein modifications have been identified to date. We describ