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Page 1
Titin Missense Variants as a Cause of Familial Dilated Cardiomyopathy.
Domínguez F, Lalaguna L, Martínez-Martín I, Piqueras-Flores J, Rasmussen TB, Zorio E, Giovinazzo G, Prados B, Ochoa JP, Bornstein B, González-López E, Velázquez-Carreras D, Pricolo MR, Gutiérrez-Agüera F, Bernal JA, Herrero-Galán E, Alegre-Cebollada J, Lara-Pezzi E, García-Pavía P. Domínguez F, et al. Circulation. 2023 May 30;147(22):1711-1713. doi: 10.1161/CIRCULATIONAHA.122.062833. Epub 2023 May 30. Circulation. 2023. PMID: 37253077 No abstract available.
[Familial approach in hereditary transthyretin cardiac amyloidosis].
García-Pavía P, Avellana P, Bornstein B, Heine-Suñer D, Cobo-Marcos M, Gómez-Bueno M, Segovia J, Alonso-Pulpón LA. García-Pavía P, et al. Rev Esp Cardiol. 2011 Jun;64(6):523-6. doi: 10.1016/j.recesp.2010.10.018. Epub 2011 Mar 24. Rev Esp Cardiol. 2011. PMID: 21439703 Free article. Spanish.
Genetic basis of end-stage hypertrophic cardiomyopathy.
Garcia-Pavia P, Vázquez ME, Segovia J, Salas C, Avellana P, Gómez-Bueno M, Vilches C, Gallardo ME, Garesse R, Molano J, Bornstein B, Alonso-Pulpon L. Garcia-Pavia P, et al. Eur J Heart Fail. 2011 Nov;13(11):1193-201. doi: 10.1093/eurjhf/hfr110. Epub 2011 Sep 6. Eur J Heart Fail. 2011. PMID: 21896538 Free article.
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. Luxán G, et al. Nat Med. 2013 Feb;19(2):193-201. doi: 10.1038/nm.3046. Epub 2013 Jan 13. Nat Med. 2013. PMID: 23314057
Erysipelas and acute myocarditis: an unusual combination.
Domínguez F, Cobo-Marcos M, Guzzo G, Cavero MA, Mirelis JG, Alonso-Pulpon L, Garcia-Pavia P. Domínguez F, et al. Can J Cardiol. 2013 Sep;29(9):1138.e3-5. doi: 10.1016/j.cjca.2012.12.021. Epub 2013 Mar 13. Can J Cardiol. 2013. PMID: 23498835
Genetics in dilated cardiomyopathy.
Garcia-Pavia P, Cobo-Marcos M, Guzzo-Merello G, Gomez-Bueno M, Bornstein B, Lara-Pezzi E, Segovia J, Alonso-Pulpon L. Garcia-Pavia P, et al. Biomark Med. 2013 Aug;7(4):517-33. doi: 10.2217/bmm.13.77. Biomark Med. 2013. PMID: 23905888 Review.
Cardiac dysfunction in mitochondrial disease. Clinical and molecular features.
Villar P, Bretón B, García-Pavía P, González-Páramos C, Blázquez A, Gómez-Bueno M, García-Silva T, García-Consuegra I, Martín MA, Garesse R, Bornstein B, Gallardo ME. Villar P, et al. Circ J. 2013;77(11):2799-806. doi: 10.1253/circj.cj-13-0557. Epub 2013 Aug 20. Circ J. 2013. PMID: 23965802 Free article.
Differential gene expression of cardiac ion channels in human dilated cardiomyopathy.
Molina-Navarro MM, Roselló-Lletí E, Ortega A, Tarazón E, Otero M, Martínez-Dolz L, Lago F, González-Juanatey JR, España F, García-Pavía P, Montero JA, Portolés M, Rivera M. Molina-Navarro MM, et al. PLoS One. 2013 Dec 5;8(12):e79792. doi: 10.1371/journal.pone.0079792. eCollection 2013. PLoS One. 2013. PMID: 24339868 Free PMC article.
281 results