Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Maite Tome‐Esteban"'
Autor:
Gherardo Finocchiaro, Emma Magavern, Gianfranco Sinagra, Euan Ashley, Michael Papadakis, Maite Tome‐Esteban, Sanjay Sharma, Iacopo Olivotto
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 6, Iss 12 (2017)
Externí odkaz:
https://doaj.org/article/0b99bc1ee8b6404d84ed21be3d9ef7b4
Autor:
Nikhil Chatrath, Joseph Westaby, Gherardo Finocchiaro, Sanjay Sharma, Maite Tome Esteban, Michael Papadakis, Mary N. Sheppard
Publikováno v:
Cardiovascular Pathology. 65:107527
Autor:
Michael Papadakis, Maite Tome-Esteban, Elijah R. Behr, B. Devine, Chiara Scrocco, Sanjay Sharma, Yael Ben-Haim, Peter W. Macfarlane
Publikováno v:
Heart rhythm. 19(1)
Background Experience with implantable loop recorders (ILRs) in Brugada syndrome (BrS) is limited. Objective The purpose of this study was to evaluate the indications and yield of ILR monitoring in a single-center BrS registry. Methods Demographic, c
Autor:
James C. Moon, S Dickie, Maite Tome-Esteban, Camelia Demetrescu, William J. McKenna, Gabriella Captur, Jose-Maria Lopez Ayala, Stefania Rosmini, Stephane Lafitte, Antonis Pantazis, Jérôme Peyrou, Oliver P Guttmann, Mariana Mirabel, H Bulluck, Patricia Reant, Guy Lloyd
Publikováno v:
Heart. 102:741-747
We hypothesised that abnormal global longitudinal strain (GLS) would predict outcome in hypertrophic cardiomyopathy (HCM) better than current echocardiographic measures.Retrospective analysis of risk markers in relation to outcomes in 472 patients wi
Autor:
Sanjay Sharma, Emma Magavern, Gianfranco Sinagra, Euan A. Ashley, Gherardo Finocchiaro, Iacopo Olivotto, Maite Tome‐Esteban, Michael Papadakis
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Felix qui potuit rerum cognoscere causas Happy is he who has been able to learn the causes of things––Virgil, Georgiche, II, 489 Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease defined clinically by the presence of unexpla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be21c0b538c7f4b355f66c011c77c040
http://hdl.handle.net/2158/1180419
http://hdl.handle.net/2158/1180419
Autor:
Antonios Pantazis, Maite Tome-Esteban, Pier D. Lambiase, Juan R. Gimeno, José Hurtado, Carla Lofiego, Bryan Mist, William J. McKenna, Perry M. Elliott
Publikováno v:
European Heart Journal. 30:2599-2605
Background Non-sustained ventricular tachycardia (NSVT) during ambulatory electrocardiographic monitoring (typically occurring at rest or during sleep) is associated with an increased risk of sudden cardiac death in patients with hypertrophic cardiom
Publikováno v:
Retina (Philadelphia, Pa.). 36(3)
Danon disease is caused by mutations in the lysosome-associated membrane protein-2 gene (LAMP2). In the eye, LAMP2 is expressed only in the retinal pigment epithelium. This study aimed to investigate the previously unreported impact of LAMP2 mutation
Autor:
Maite Tome-Esteban, William J. McKenna, Stephane Lafitte, Silvia Castelletti, Petros Syrris, James C. Moon, Stefania Rosmini, Arnaud D Hauer, Patricia Reant, Mun Hong Cheang, Antonis Pantazis, Jérôme Peyrou
Publikováno v:
The international journal of cardiovascular imaging. 32(4)
The aim of this cohort study was to evaluate the value of echocardiographic multilayer strain analysis in the identification of arrhythmogenic cardiomyopathy (AC) in its earliest stages in which sudden cardiac death can occurs. Twenty seven asymptoma
Autor:
Catherine W.M. Ong, Joanna C. Porter, Vimal Patel, Maite Tome-Esteban, Przemyslaw J. Pabisiak, Liku B. Tezera, Robert H. Gilman, Tarangini Sathyamoorthy, Sara Brilha, Rachel Moores, Cesar Ugarte-Gil, Paul T. Elkington, Jon S. Friedland
Publikováno v:
PLoS Pathogens
PLoS Pathogens, Vol 11, Iss 5, p e1004917 (2015)
PLoS Pathogens, Vol 11, Iss 5, p e1004917 (2015)
Pulmonary cavities, the hallmark of tuberculosis (TB), are characterized by high mycobacterial load and perpetuate the spread of M. tuberculosis. The mechanism of matrix destruction resulting in cavitation is not well defined. Neutrophils are emergin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dadfd59053d4647b841ea3f9e873af4a
https://eprints.soton.ac.uk/377480/
https://eprints.soton.ac.uk/377480/
Autor:
Sharon Jenkins, Daniel Sado, Petros Syrris, Maite Tome-Esteban, Anna S Herrey, Gabriella Captur, William J. McKenna, Arthur Nasis, Viviana Maestrini, Mariana Mirabel, Silvia Castelletti, Charlotte Manisty, Perry M. Elliott, James C. Moon, Patricia Reant
Publikováno v:
Journal of Cardiovascular Magnetic Resonance
BACKGROUND: Sarcomeric gene mutations cause hypertrophic cardiomyopathy (HCM). In gene mutation carriers without left ventricular (LV) hypertrophy (G + LVH-), subclinical imaging biomarkers are recognized as predictors of overt HCM, consisting of ant
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38db054cdd8ecf3de38504fbfa0cadd7
http://hdl.handle.net/11573/970040
http://hdl.handle.net/11573/970040