búsquedas

Cardiopatías Familiares

Publicaciones destacadas recientes

  • Mutations in the NOTCH pathway regulator MIB1 cause left ventricular noncompaction cardiomyopathy.
    Luxán G, Casanova JC, Martínez-Poveda B, Prados B, D'Amato G, MacGrogan D, Gonzalez-Rajal A, Dobarro D, Torroja C, Martinez F, Izquierdo-García JL, Fernández-Friera L, Sabater-Molina M, Kong YY, Pizarro G, Ibañez B, Medrano C, García-Pavía P, Gimeno JR, Monserrat L, Jiménez-Borreguero LJ, de la Pompa JL.
    Nat Med. 2013 Feb;19(2):193-201. doi: 10.1038/nm.3046. Epub 2013 Jan 13. (ARTICULO)(IF 22.462)
  • Left ventricular hypertrophy in Fabry disease: a practical approach to diagnosis.
    Yousef Z, Elliott PM, Cecchi F, Escoubet B, Linhart A, Monserrat L, Namdar M, Weidemann F.
    Eur Heart J 2012; Jun 26 (Epub ahead of print) (ARTICULO)(IF 10.478) - Cardiotrophin-1 plasma levels are associated with the severity of hypertrophy in hypertrophic cardiomyopathy. Monserrat L, López B, González A, Hermida M, Fernández X, Ortiz M, Barriales-Villa R, Castro-Beiras A, Díez J. Eur Heart J. 2011;32:177-83. (ARTICULO)(IF 10.487)
  • Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases.
    Charron P, Arad M, Arbustini E, Basso C, Bilinska Z, Elliott P, Helio T, Keren A, McKenna WJ, Monserrat L, Pankuweit S, Perrot A, Rapezzi C, Ristic A, Seggewiss H, van Langen I, Tavazzi L.
    Eur Heart J 2010 Nov;31:2715-26. (ARTICULO)(IF 10.046).
  • Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases.
    Elliott P, Andersson B, Arbustini E, Bilinska Z, Cecchi F, Charron P, Dubourg O, Kühl U, Maisch B, McKenna WJ, Monserrat L, Pankuweit S, Rapezzi C, Seferovic P, Tavazzi L, Keren A.
    Eur Heart J 2008; 29:270-6. (ARTICULO)(IF 8.917)
  • Prevelence of Fabry disease in a cohort of 508 unrelated patients with hypertrophic cardiomyopathy.
    Monserrat L, Gimeno-Blanes JR, Marín F, Hermida-Prieto M, García-Honrubia A, Perez I, Fernandez X, de Nicolas R, de la Morena G, Paya E, Yagüe J, Egido J.
    J Am Coll Cardiol 2007; 50:2399-403. (ARTICULO)(IF 11.054)
  • Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects.
    Monserrat L, Hermida-Prieto M, Fernandez X, Rodríguez I, Dumont C, Cazón L, Cuesta MG, Gonzalez-Juanatey C, Peteiro J, Alvarez N, Penas-Lado M, Castro-Beiras A.
    Eur Heart J. 2007 Aug;28(16):1953-61. (ARTICULO)(IF 7.924)
  • Interpretation of electrocardiographic abnormalities in hypertrophic cardiomyopathy with cardiac magnetic resonance.
    Dumont CA, Monserrat L, Soler R, Rodríguez E, Fernandez X, Peteiro J, Bouzas A, Bouzas B, Castro-Beiras A.
    Eur Heart J. 2006;27:1725-31. (ARTICULO)(IF 7.286)
  • Gene mutations in apical hypertrophic cardiomyopathy.
    Arad M, Penas Lado M, Monserrat L, Maron BJ, Sherrid M, Ho CY, Barr S, Karim A, Olson TM, Kamisago M, Seidman JG, Seidman CE.
    Circulation. 2005 Nov 1;112(18):2805-11. (ARTICULO)(IF 11.362)
cierre
Logotipo Servizo Galego de Saude Logotipo de Complexo Hospitalario Universitario A Coruña Logotipo Universidade da Coruña Logotipo Fundación do Complexo Hospitalario Universitario A Coruña Consellería de innovación