Publicaciones (18) Publicaciones en las que ha participado algún/a investigador/a

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. Efecto de un programa de formación en atención primaria sobre la optimización del tratamiento con bloqueadores beta en pacientes ancianos con insuficiencia cardiaca

    Revista Espanola de Cardiologia, Vol. 63, Núm. 6, pp. 677-685

  5. Exon-skipping brain natriuretic peptide variant is overexpressed in failing myocardium and attenuates brain natriuretic peptide production in vitro

    Experimental Biology and Medicine, Vol. 235, Núm. 8, pp. 941-951

  6. Identification of candidate genes potentially relevant to chamber-specific remodeling in postnatal ventricular myocardium

    Journal of Biomedicine and Biotechnology, Vol. 2010

  7. Incidence and risk factors for nonmelanoma skin cancer after heart transplantation

    Transplantation Proceedings, Vol. 42, Núm. 8, pp. 3001-3005

  8. 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

  9. Prevalence and severity of renal dysfunction among 1062 heart transplant patients according to criteria based on serum creatinine and estimated glomerular filtration rate: Results from the CAPRI study

    Clinical Transplantation, Vol. 24, Núm. 4

  10. Prevalencia, causas y pronóstico de las «falsas alarmas» al laboratorio de hemodinámica en pacientes con sospecha de infarto de miocardio con elevación del segmento ST

    Revista Espanola de Cardiologia, Vol. 63, Núm. 5, pp. 518-527

  11. Risk factors associated with moderate-to-severe renal dysfunction among heart transplant patients: Results from the CAPRI study

    Clinical Transplantation, Vol. 24, Núm. 5, pp. 194-200

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

    BMC Medical Genetics, Vol. 11, Núm. 1

  13. Sobre la utilidad clínica del diagnóstico genético

    Galicia Clínica, Vol. 71, Núm. 4, pp. 148-150

  14. 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

  15. The effect of post-discharge educational intervention on patients in achieving objectives in modifiable risk factors six months after discharge following an episode of acute coronary syndrome, (CAM-2 Project): a randomized controlled trial

    Health and Quality of Life Outcomes, Vol. 8

  16. The prognosis of noncutaneous, nonlymphomatous malignancy after heart transplantation: Data from the Spanish post-heart transplant tumour registry

    Transplantation Proceedings, Vol. 42, Núm. 8, pp. 3011-3013

  17. The source of error in the estimation of intertwin birth weight discordance

    Journal of Perinatal Medicine, Vol. 38, Núm. 6, pp. 671-674

  18. 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