Publicacións nas que colabora con Alfonso Castro Beiras (57)

2015

  1. 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

  2. Genetics of cardiomyopathies: Novel perspectives with next generation sequencing

    Current Pharmaceutical Design, Vol. 21, Núm. 4, pp. 418-430

2013

  1. Comparison of the performance of the CRUSADE, ACUITY-HORIZONS, and ACTION bleeding risk scores in STEMI undergoing primary PCI: Insights from a cohort of 1391 patients

    European Heart Journal: Acute Cardiovascular Care, Vol. 2, Núm. 1, pp. 19-26

  2. Somatic MYH7, MYBPC3, TPM1, TNNT2 and TNNI3 mutations in sporadic hypertrophic cardiomyopathy

    Circulation Journal, Vol. 77, Núm. 9, pp. 2358-2365

  3. p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient

    Heart Rhythm, Vol. 10, Núm. 2, pp. 264-272

2012

  1. 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

  1. 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

  1. '2' Much mitral tissue

    European Journal of Echocardiography, Vol. 11, Núm. 2, pp. 189

  2. Disease: Cardiomyopathy, hypertrophic

    Human Genetics

  3. Disease: Cardiomyopathy, hypertrophic

    Human Genetics

  4. Insights into genotype-phenotype correlation in hypertrophic cardiomyopathy. Findings from 18 Spanish families with a single mutation in MYBPC3

    Heart, Vol. 96, Núm. 24, pp. 1980-1984

  5. Pulmonary vein stenosis after lung transplantation successfully treated with stent implantation

    Circulation, Vol. 122, Núm. 25, pp. 2745-2747

  6. Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

    BMC Medical Genetics, Vol. 11, Núm. 1

2009

  1. 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

  2. Natural history of a giant coronary aneurysm with spontaneous dissection

    Clinical Cardiology, Vol. 32, Núm. 12

2008

  1. Large scale analysis of HCM mutations in sudden cardiac death

    Forensic Science International: Genetics Supplement Series, Vol. 1, Núm. 1, pp. 549-550

  2. 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

  1. Comparison of 2- and 3-Dimensional Exercise Echocardiography for the Detection of Coronary Artery Disease

    Journal of the American Society of Echocardiography, Vol. 20, Núm. 8, pp. 959-967

  2. 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

  3. Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

    European Heart Journal, Vol. 28, Núm. 16, pp. 1953-1961