Publicacións nas que colabora con Alfonso Castro Beiras (52)

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

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

  2. 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. Disease: Cardiomyopathy, hypertrophic

    Human Genetics

  2. Disease: Cardiomyopathy, hypertrophic

    Human Genetics

  3. 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

  4. 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

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

  4. Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN - 42 C>G mutation

    European Journal of Heart Failure, Vol. 9, Núm. 1, pp. 37-43

  5. Progress in idiopathic dilated cardiomyopathy: From genotype to clinical phenotype

    Revista Espanola de Cardiologia Suplementos, Vol. 7, Núm. F

  6. Relation of Left Ventricular Chamber Stiffness at Rest to Exercise Capacity in Hypertrophic Cardiomyopathy

    American Journal of Cardiology, Vol. 99, Núm. 10, pp. 1454-1457

  7. Significado clínico del realce tardío de gadolinio con resonancia magnética en pacientes con miocardiopatía hipertrófica

    Revista Espanola de Cardiologia, Vol. 60, Núm. 1, pp. 15-23