Publicaciones en las que colabora con Manuel Hermida Prieto (26)

2013

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

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

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. Diagnóstico genético en cardiopatías familiares

    Actualización en cardiología (Servicio de Publicaciones)

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

    BMC Medical Genetics, Vol. 11, Núm. 1

  6. The R820W mutation in the MYBPC3 gene, associated with hypertrophic cardiomyopathy in cats, causes hypertrophic cardiomyopathy and left ventricular non-compaction in humans

    International Journal of Cardiology, Vol. 145, Núm. 2, pp. 405-407

  7. 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

  1. Miocardiopatía hipertrófica. Estudio del gen de la troponina T en 127 familias españolas

    Revista Espanola de Cardiologia, Vol. 62, Núm. 12, pp. 1473-1477

  2. 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. Apical hypertrophic cardiomyopathy and left ventricular non-compaction: two faces of the same disease

    Heart, Vol. 94, Núm. 10, pp. 1253

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

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

  3. Reply

    Journal of the American College of Cardiology

  4. 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. Erratum: Mutaciones en el gen de la cadena pesada de la betamiosina en pacientes con miocardiopatía hipertrófica (Revista Española de Cardiologia (2006) 59 (1008-18))

    Revista Espanola de Cardiologia

  2. 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

  3. 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

  4. Prevalence of Fabry Disease in a Cohort of 508 Unrelated Patients With Hypertrophic Cardiomyopathy

    Journal of the American College of Cardiology, Vol. 50, Núm. 25, pp. 2399-2403

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

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