Barriales-Villa R - Search Results

1

Severe cardiac conduction disturbances and pacemaker implantation in patients with hypertrophic cardiomyopathy.

Barriales-Villa R, Centurión-Inda R, Fernández-Fernández X, Ortiz MF, Pérez-Alvarez L, Rodríguez García I, Hermida-Prieto M, Monserrat L. Barriales-Villa R, et al. Rev Esp Cardiol. 2010 Aug;63(8):985-8. doi: 10.1016/s1885-5857(10)70192-4. Rev Esp Cardiol. 2010. PMID: 20738943 Free article. English, Spanish.

2

2023 ESC Guidelines for the management of cardiomyopathies.

Arbelo E, Protonotarios A, Gimeno JR, Arbustini E, Barriales-Villa R, Basso C, Bezzina CR, Biagini E, Blom NA, de Boer RA, De Winter T, Elliott PM, Flather M, Garcia-Pavia P, Haugaa KH, Ingles J, Jurcut RO, Klaassen S, Limongelli G, Loeys B, Mogensen J, Olivotto I, Pantazis A, Sharma S, Van Tintelen JP, Ware JS, Kaski JP; ESC Scientific Document Group. Arbelo E, et al. Eur Heart J. 2023 Oct 1;44(37):3503-3626. doi: 10.1093/eurheartj/ehad194. Eur Heart J. 2023. PMID: 37622657 No abstract available.

3

Treatment of hypertrophic cardiomyopathy.

Penas-Lado M, Barriales-Villa R, Monserrat L. Penas-Lado M, et al. Circulation. 2003 Apr 29;107(16):e110; auhor reply e110. doi: 10.1161/01.CIR.0000067695.32364.37. Circulation. 2003. PMID: 12719296 No abstract available.

4

Apical hypertrophic cardiomyopathy and left ventricular non-compaction: two faces of the same disease.

Monserrat L, Barriales-Villa R, Hermida-Prieto M. Monserrat L, et al. Heart. 2008 Oct;94(10):1253. doi: 10.1136/hrt.2008.154047. Heart. 2008. PMID: 18801786 No abstract available.

5

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.

6

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.

7

Brugada syndrome.

Barriales-Villa R, Ortiz MF, García DA. Barriales-Villa R, et al. Rev Esp Cardiol. 2010 May;63(5):620; author reply 620. doi: 10.1016/s1885-5857(10)70131-6. Rev Esp Cardiol. 2010. PMID: 20450864 Free article. No abstract available.

8

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.

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):483. Hum Genet. 2010. PMID: 21488259 No abstract available.

10

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.

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