Zobrazeno 1 - 10
of 61
pro vyhledávání: '"Juan Gabriel, Martínez-Martínez"'
Prognostic impact of the findings of the genetic test in left dominant arrhythmogenic cardiomyopathy
Autor:
Laura García-Cano, José Miguel Martín-Torres, Amaya García-Fernández, Eloísa Feliu-Rey, Juan Gabriel Martínez-Martínez, Juan Miguel Ruiz-Nodar
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 51, Iss , Pp 101367- (2024)
Background: The diagnosis of left dominant arrhythmogenic cardiomyopathy (LDAC) is sometimes complex. The Padua group recently published a document with criteria to identify patients with LDAC, requiring a compatible genetic variant for diagnosis. Du
Externí odkaz:
https://doaj.org/article/db67ab63bae34ac39177fe631c22cd50
Autor:
Marta Herrero-Brocal, Francisco Marín, Laura Valverde, Ana M. García-Barrios, Laura Fuertes, Cristina Cambra, Fernando Torres-Mezcua, Ignacio Hortelano, Beatriz Villamia, María Asunción Esteve-Pastor, Esteban Orenes-Piñero, Juan Gabriel Martínez Martínez, José Miguel Rivera-Caravaca, Juan M. Ruiz-Nodar
Publikováno v:
International Journal of Cardiology: Heart & Vasculature, Vol 46, Iss , Pp 101209- (2023)
The introduction of high-sensitivity troponin (hsTn) assays has reduced the diagnosis of unstable angina (UA) in favor of non-ST elevation myocardial infarction (NSTEMI) in the context of non-ST elevation acute coronary syndrome (NSTEACS). It is uncl
Externí odkaz:
https://doaj.org/article/d0e31fa62a6d4fffbab2c2ea3576836e
Autor:
Laura García-Cano, Thomas André Brouzet, Amaya García-Fernández, José Luis Ibáñez-Criado, Marta Monteagudo-Viana, Alicia Ibáñez-Criado, Juan Gabriel Martínez-Martínez
Publikováno v:
International Journal of Arrhythmia, Vol 22, Iss 1, Pp 1-4 (2021)
Abstract Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe hereditary channelopathy characterized by the presence of ventricular arrhythmias triggered by adrenergic stimuli, usually diagnosed in the first two decades
Externí odkaz:
https://doaj.org/article/87d78106d6a84cbe952a66d3bb7a5fda
Autor:
Laura García-Cano, Eloísa Feliu-Rey, Juan Miguel Ruiz-Nodar, José Miguel Martín-Torres, Amaya García-Fernández, Juan Gabriel Martínez-Martínez
Publikováno v:
J Cardiol Cases
Arrhythmogenic cardiomyopathy is a hereditary disease characterized by the replacement of the myocardium by fibrofatty tissue. In recent years, three patterns have been described: the classic right variant, the biventricular variant, and the variant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e6b6d3468b2a8eecd0d6e802a85b4cc
https://europepmc.org/articles/PMC10066412/
https://europepmc.org/articles/PMC10066412/
Autor:
Thomas Brouzet, Juan Gabriel Martínez-Martínez, Amaya García-Fernández, Alicia Ibáñez-Criado, Marta Monteagudo-Viana, José Luis Ibáñez-Criado, Laura García-Cano
Publikováno v:
International Journal of Arrhythmia, Vol 22, Iss 1, Pp 1-4 (2021)
Background Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a severe hereditary channelopathy characterized by the presence of ventricular arrhythmias triggered by adrenergic stimuli, usually diagnosed in the first two decades of life.
Autor:
Alicia Ibáñez-Criado, Óscar Moreno-Pérez, Juan Gabriel Martínez-Martínez, Cristina Cambra-Poveda, Pablo Ramos-Ruiz, Amaya García-Fernández
Publikováno v:
Revista Española de Cardiología (English Edition)
Autor:
Luna Carrillo, Amaya García-Fernández, Juan Gabriel Martínez Martínez, Rafal Moscicki, Eloisa Feliu, Juan M. Ruiz-Nodar
Publikováno v:
Revista Española de Cardiología. 73:885-892
Resumen Introduccion y objetivos Recientemente, la miocardiopatia arritmogenica del ventriculo izquierdo (MCAVI) ha sido reconocida como parte del espectro de la miocardiopatia arritmogenica. Se caracteriza por el reemplazo fibroadiposo de la pared d
Autor:
Gerard Loughlin, Marta Pachón, José Luis Martínez‐Sande, José Luis Ibáñez, Teresa Bastante, Joaquín Osca Asensi, Laila González Melchor, Juan Gabriel Martínez‐Martínez, Javier Cuesta, Miguel A. Arias
Publikováno v:
JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
INTRODUCTION: Device infections constitute a major complication of transvenous pacemakers. Mechanical heart valves (MHV) increase the risk of infective endocarditis (IE) and pacemaker infection, requiring lifelong vitamin K-antagonists (VKA), which m
Autor:
Pablo, Gil-Perez, Juan Miguel, Ruiz-Nodar, María Asunción, Esteve-Pastor, Ignacio, Hortelano, Beatriz, Villamía, Nuria, Vicente-Ibarra, Esteban, Orenes-Piñero, Manuel Jesús, Macías, Laura, Núñez-Martínez, Luna, Carrillo, Elena, Candela, Andrea, Véliz-Martínez, Cecilia, López-García, Juan Gabriel, Martínez-Martínez, José Miguel, Rivera-Caravaca, Francisco, Marín
Publikováno v:
Diabetes research and clinical practice. 184
We investigated the impact of diabetes mellitus (DM) in acute coronary syndrome (ACS) patients, and the 2-year prognosis based on antiplatelet therapy.This is a prospective and multicenter registry including hospitalized ACS patients. Clinical manage
Autor:
Juan Quiles-Granado, Laura Fuertes-Kenneally, Jessica Sánchez-Quiñones, Juan Gabriel Martínez-Martínez
Publikováno v:
European Heart Journal: Case Reports
Background Platypnoea–orthodeoxia syndrome (POS) is a rare condition characterized by hypoxaemia and dyspnoea when changing from a recumbent to an upright position. Diagnosis requires a high clinical suspicion and is often underdiagnosed. Case summ