Castro-Beiras A - Search Results

1

p.D1690N Nav1.5 rescues p.G1748D mutation gating defects in a compound heterozygous Brugada syndrome patient.

Núñez L, Barana A, Amorós I, de la Fuente MG, Dolz-Gaitón P, Gómez R, Rodríguez-García I, Mosquera I, Monserrat L, Delpón E, Caballero R, Castro-Beiras A, Tamargo J. Núñez L, et al. Heart Rhythm. 2013 Feb;10(2):264-72. doi: 10.1016/j.hrthm.2012.10.025. Epub 2012 Oct 18. Heart Rhythm. 2013. PMID: 23085483

2

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.

3

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

4

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.

5

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. Monserrat L, et al. Eur Heart J. 2011 Jan;32(2):177-83. doi: 10.1093/eurheartj/ehq400. Epub 2010 Nov 8. Eur Heart J. 2011. PMID: 21059734 Free PMC article.

6

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.

Rodriguez-Garcia MI, Monserrat L, Ortiz M, Fernández X, Cazón L, Núñez L, Barriales-Villa R, Maneiro E, Veira E, Castro-Beiras A, Hermida-Prieto M. Rodriguez-Garcia MI, et al. Hum Genet. 2010 Apr;127(4):483. Hum Genet. 2010. PMID: 21488259 No abstract available.

7

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.

Rodriguez-Garcia MI, Monserrat L, Ortiz M, Fernández X, Cazón L, Núñez L, Barriales-Villa R, Maneiro E, Veira E, Castro-Beiras A, Hermida-Prieto M. Rodriguez-Garcia MI, et al. Hum Genet. 2010 Apr;127(4):483. Hum Genet. 2010. PMID: 21488306 No abstract available.

8

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.

Rodriguez-Garcia MI, Monserrat L, Ortiz M, Fernández X, Cazón L, Núñez L, Barriales-Villa R, Maneiro E, Veira E, Castro-Beiras A, Hermida-Prieto M. Rodriguez-Garcia MI, et al. Hum Genet. 2010 Apr;127(4):484. Hum Genet. 2010. PMID: 21488307 No abstract available.

9

Novel human pathological mutations. Gene symbol: MYBPC3. Disease: cardiomyopathy, hypertrophic.

Rodriguez-Garcia MI, Monserrat L, Ortiz M, Fernández X, Cazón L, Núñez L, Barriales-Villa R, Maneiro E, Veira E, Castro-Beiras A, Hermida-Prieto M. Rodriguez-Garcia MI, et al. Hum Genet. 2010 Apr;127(4):484. Hum Genet. 2010. PMID: 21488308 No abstract available.

10

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

Núñez L, Gimeno-Blanes JR, Rodríguez-García MI, Monserrat L, Zorio E, Coats C, McGregor CG, Hernandez del Rincón JP, Castro-Beiras A, Hermida-Prieto M. Núñez L, et al. Circ J. 2013;77(9):2358-65. doi: 10.1253/circj.cj-13-0294. Epub 2013 Jun 19. Circ J. 2013. PMID: 23782526 Free article. Clinical Trial.

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