Publicaciones en las que colabora con Lorenzo Monserrat Iglesias (29)
2023
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Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry
European Heart Journal - Quality of Care and Clinical Outcomes, Vol. 9, Núm. 1, pp. 42-53
2021
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Clinical utility of genetic testing in patients with dilated cardiomyopathy
Medicina Clinica, Vol. 156, Núm. 10, pp. 485-495
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Differences between familial and sporadic dilated cardiomyopathy: ESC EORP Cardiomyopathy & Myocarditis registry
ESC Heart Failure, Vol. 8, Núm. 1, pp. 95-105
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Prognostic value of reduced heart rate reserve during exercise in hypertrophic cardiomyopathy
Journal of Clinical Medicine, Vol. 10, Núm. 7
2020
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Prognostic implications of pathogenic truncating variants in the TTN gene
International Journal of Cardiology, Vol. 316, pp. 180-183
2016
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European cardiomyopathy pilot registry: EURObservational research programme of the European society of cardiology
European Heart Journal, Vol. 37, Núm. 2, pp. 164-173
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Prognostic role of stress echocardiography in hypertrophic cardiomyopathy: The International Stress Echo Registry
International Journal of Cardiology, Vol. 219, pp. 331-338
2015
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Exercise echocardiography and cardiac magnetic resonance imaging to predict outcome in patients with hypertrophic cardiomyopathy
European Heart Journal Cardiovascular Imaging, Vol. 16, Núm. 4, pp. 423-432
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Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain
Heart, Vol. 101, Núm. 13, pp. 1047-1053
2014
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A novel clinical risk prediction model for sudden cardiac death in hypertrophic cardiomyopathy (HCM Risk-SCD)
European Heart Journal, Vol. 35, Núm. 30, pp. 2010-2020
2012
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Prognostic value of exercise echocardiography in patients with hypertrophic cardiomyopathy
Journal of the American Society of Echocardiography, Vol. 25, Núm. 2, pp. 182-189
2011
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Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy
European Heart Journal, Vol. 32, Núm. 2, pp. 177-183
2010
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Disease: Cardiomyopathy, hypertrophic
Human Genetics
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Disease: Cardiomyopathy, hypertrophic
Human Genetics
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Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy
BMC Medical Genetics, Vol. 11, Núm. 1
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Trastornos graves de la conducción cardiaca e implante de marcapasos en pacientes con miocardiopatía hipertrófica
Revista Espanola de Cardiologia, Vol. 63, Núm. 8, pp. 985-988
2009
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Mutación en homocigosis en el gen MYBPC3 asociada a fenotipos severos y alto riesgo de muerte súbita en una familia con miocardiopatía hipertrófica
Revista Espanola de Cardiologia, Vol. 62, Núm. 5, pp. 572-575
2008
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Reply
Journal of the American College of Cardiology
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Sudden death in a patient with lamin A/C gene mutation and near normal left ventricular systolic function
International Journal of Cardiology, Vol. 126, Núm. 1, pp. 136-137
2007
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Left Ventricular Asynchrony in Patients with Hypertrophic Cardiomyopathy: Its Determinants and its Relation to Left Ventricular Function
Journal of the American Society of Echocardiography, Vol. 20, Núm. 11, pp. 1247-1252