Castro-Beiras A - Search Results

1

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

Medin M, Hermida-Prieto M, Monserrat L, Laredo R, Rodriguez-Rey JC, Fernandez X, Castro-Beiras A. Medin M, et al. Eur J Heart Fail. 2007 Jan;9(1):37-43. doi: 10.1016/j.ejheart.2006.04.007. Epub 2006 Jul 7. Eur J Heart Fail. 2007. PMID: 16829191 Free article.

2

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

Hermida-Prieto M, Monserrat L, Castro-Beiras A, Laredo R, Soler R, Peteiro J, Rodríguez E, Bouzas B, Alvarez N, Muñiz J, Crespo-Leiro M. Hermida-Prieto M, et al. Am J Cardiol. 2004 Jul 1;94(1):50-4. doi: 10.1016/j.amjcard.2004.03.029. Am J Cardiol. 2004. PMID: 15219508 Free article.

3

[Familial dilated cardiomyopathy: current status and clinical benefits of basic research].

Castro Beiras A, Monserrat L, Hermida M. Castro Beiras A, et al. Rev Esp Cardiol. 2003;56 Suppl 1:7-12. Rev Esp Cardiol. 2003. PMID: 15626357 Free article. Review. Spanish.

4

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. Dumont CA, et al. Eur Heart J. 2006 Jul;27(14):1725-31. doi: 10.1093/eurheartj/ehl101. Epub 2006 Jun 14. Eur Heart J. 2006. PMID: 16774982

5

[Beta-myosin heavy-chain gene mutations in patients with hypertrophic cardiomyopathy].

Laredo R, Monserrat L, Hermida-Prieto M, Fernández X, Rodríguez I, Cazón L, Alvariño I, Dumont C, Piñón P, Peteiro J, Bouzas B, Castro-Beiras A. Laredo R, et al. Rev Esp Cardiol. 2006 Oct;59(10):1008-18. doi: 10.1157/13093977. Rev Esp Cardiol. 2006. PMID: 17125710 Free article. Spanish.

6

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. Monserrat L, et al. Eur Heart J. 2007 Aug;28(16):1953-61. doi: 10.1093/eurheartj/ehm239. Epub 2007 Jul 4. Eur Heart J. 2007. PMID: 17611253

7

[Familial dilated cardiomyopathy in patients transplanted for idiopathic dilated cardiomyopathy].

Monserrat L, Hermida M, Bouzas B, Mosquera I, Mahon N, Peteiro J, Alvarez N, Penas-Lado M, Crespo M, Castro-Beiras A. Monserrat L, et al. Rev Esp Cardiol. 2002 Jul;55(7):725-32. doi: 10.1016/s0300-8932(02)76691-8. Rev Esp Cardiol. 2002. PMID: 12113700 Free article. Spanish.

8

Standard mutation nomenclature in hypertrophic cardiomyopathy: an urgent need.

Hermida-Prieto M, Laredo R, Monserrat L, Castro-Beiras A. Hermida-Prieto M, et al. J Am Coll Cardiol. 2005 Jul 19;46(2):380-1; author reply 381-2. doi: 10.1016/j.jacc.2005.04.025. J Am Coll Cardiol. 2005. PMID: 16022973 Free article. No abstract available.

9

A homozygous MYBPC3 gene mutation associated with a severe phenotype and a high risk of sudden death in a family with hypertrophic cardiomyopathy.

Ortiz MF, Rodríguez-García MI, Hermida-Prieto M, Fernández X, Veira E, Barriales-Villa R, Castro-Beiras A, Monserrat L. Ortiz MF, et al. Rev Esp Cardiol. 2009 May;62(5):572-5. doi: 10.1016/s1885-5857(09)71841-9. Rev Esp Cardiol. 2009. PMID: 19406073 Free article. English, Spanish.

10

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

Rodríguez-García MI, Monserrat L, Ortiz M, Fernández X, Cazón L, Núñez L, Barriales-Villa R, Maneiro E, Veira E, Castro-Beiras A, Hermida-Prieto M. Rodríguez-García MI, et al. BMC Med Genet. 2010 Apr 30;11:67. doi: 10.1186/1471-2350-11-67. BMC Med Genet. 2010. PMID: 20433692 Free PMC article.

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