Barriales-Villa R - Search Results

1

Formin Homology 2 Domain Containing 3 (FHOD3) Is a Genetic Basis for Hypertrophic Cardiomyopathy.

Ochoa JP, Sabater-Molina M, García-Pinilla JM, Mogensen J, Restrepo-Córdoba A, Palomino-Doza J, Villacorta E, Martinez-Moreno M, Ramos-Maqueda J, Zorio E, Peña-Peña ML, García-Granja PE, Rodríguez-Palomares JF, Cárdenas-Reyes IJ, de la Torre-Carpente MM, Bautista-Pavés A, Akhtar MM, Cicerchia MN, Bilbao-Quesada R, Mogollón-Jimenez MV, Salazar-Mendiguchía J, Mesa Latorre JM, Arnaez B, Olavarri-Miguel I, Fuentes-Cañamero ME, Lamounier A Jr, Pérez Ruiz JM, Climent-Payá V, Pérez-Sanchez I, Trujillo-Quintero JP, Lopes LR, Repáraz-Andrade A, Marín-Iglesias R, Rodriguez-Vilela A, Sandín-Fuentes M, Garrote JA, Cortel-Fuster A, Lopez-Garrido M, Fontalba-Romero A, Ripoll-Vera T, Llano-Rivas I, Fernandez-Fernandez X, Isidoro-García M, Garcia-Giustiniani D, Barriales-Villa R, Ortiz-Genga M, García-Pavía P, Elliott PM, Gimeno JR, Monserrat L. Ochoa JP, et al. J Am Coll Cardiol. 2018 Nov 13;72(20):2457-2467. doi: 10.1016/j.jacc.2018.10.001. J Am Coll Cardiol. 2018. PMID: 30442288 Free article.

2

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.

3

[Transient left ventricular apical ballooning without coronary stenoses syndrome: importance of the intraventricular pressure gradient].

Barriales Villa R, Bilbao Quesada R, Iglesias Río E, Bayón Meleiro N, Mantilla González R, Penas Lado M. Barriales Villa R, et al. Rev Esp Cardiol. 2004 Jan;57(1):85-8. Rev Esp Cardiol. 2004. PMID: 14746723 Free article. Spanish.

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

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.

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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