Pantazis A - Search Results

1

Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy.

Kaski JP, Syrris P, Esteban MT, Jenkins S, Pantazis A, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Among authors: pantazis a. Circ Cardiovasc Genet. 2009 Oct;2(5):436-41. doi: 10.1161/CIRCGENETICS.108.821314. Epub 2009 Jul 16. Circ Cardiovasc Genet. 2009. PMID: 20031618

2

Clinical expression of plakophilin-2 mutations in familial arrhythmogenic right ventricular cardiomyopathy.

Syrris P, Ward D, Asimaki A, Sen-Chowdhry S, Ebrahim HY, Evans A, Hitomi N, Norman M, Pantazis A, Shaw AL, Elliott PM, McKenna WJ. Syrris P, et al. Among authors: pantazis a. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA.105.561654. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415378 Free article.

3

Mutational heterogeneity, modifier genes, and environmental influences contribute to phenotypic diversity of arrhythmogenic cardiomyopathy.

Sen-Chowdhry S, Syrris P, Pantazis A, Quarta G, McKenna WJ, Chambers JC. Sen-Chowdhry S, et al. Among authors: pantazis a. Circ Cardiovasc Genet. 2010 Aug;3(4):323-30. doi: 10.1161/CIRCGENETICS.109.935262. Epub 2010 Jun 22. Circ Cardiovasc Genet. 2010. PMID: 20570917

4

Prevalence of desmosomal protein gene mutations in patients with dilated cardiomyopathy.

Elliott P, O'Mahony C, Syrris P, Evans A, Rivera Sorensen C, Sheppard MN, Carr-White G, Pantazis A, McKenna WJ. Elliott P, et al. Among authors: pantazis a. Circ Cardiovasc Genet. 2010 Aug;3(4):314-22. doi: 10.1161/CIRCGENETICS.110.937805. Circ Cardiovasc Genet. 2010. PMID: 20716751

5

Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria.

Quarta G, Muir A, Pantazis A, Syrris P, Gehmlich K, Garcia-Pavia P, Ward D, Sen-Chowdhry S, Elliott PM, McKenna WJ. Quarta G, et al. Among authors: pantazis a. Circulation. 2011 Jun 14;123(23):2701-9. doi: 10.1161/CIRCULATIONAHA.110.976936. Epub 2011 May 23. Circulation. 2011. PMID: 21606390

6

The binary endocardial appearance is a poor discriminator of Anderson-Fabry disease from familial hypertrophic cardiomyopathy.

Kounas S, Demetrescu C, Pantazis AA, Keren A, Lee PJ, Hughes D, Mehta A, Elliott PM. Kounas S, et al. Among authors: pantazis aa. J Am Coll Cardiol. 2008 May 27;51(21):2058-61. doi: 10.1016/j.jacc.2008.02.046. J Am Coll Cardiol. 2008. PMID: 18498962 Free article.

7

Exercise-induced ventricular arrhythmias and risk of sudden cardiac death in patients with hypertrophic cardiomyopathy.

Gimeno JR, Tomé-Esteban M, Lofiego C, Hurtado J, Pantazis A, Mist B, Lambiase P, McKenna WJ, Elliott PM. Gimeno JR, et al. Among authors: pantazis a. Eur Heart J. 2009 Nov;30(21):2599-605. doi: 10.1093/eurheartj/ehp327. Epub 2009 Aug 17. Eur Heart J. 2009. PMID: 19689975

8

Mutations in the Lamin A/C gene mimic arrhythmogenic right ventricular cardiomyopathy.

Quarta G, Syrris P, Ashworth M, Jenkins S, Zuborne Alapi K, Morgan J, Muir A, Pantazis A, McKenna WJ, Elliott PM. Quarta G, et al. Among authors: pantazis a. Eur Heart J. 2012 May;33(9):1128-36. doi: 10.1093/eurheartj/ehr451. Epub 2011 Dec 23. Eur Heart J. 2012. PMID: 22199124

9

A validation study of the 2003 American College of Cardiology/European Society of Cardiology and 2011 American College of Cardiology Foundation/American Heart Association risk stratification and treatment algorithms for sudden cardiac death in patients with hypertrophic cardiomyopathy.

O'Mahony C, Tome-Esteban M, Lambiase PD, Pantazis A, Dickie S, McKenna WJ, Elliott PM. O'Mahony C, et al. Among authors: pantazis a. Heart. 2013 Apr;99(8):534-41. doi: 10.1136/heartjnl-2012-303271. Epub 2013 Jan 22. Heart. 2013. PMID: 23339826

10

Heart failure in patients with arrhythmogenic right ventricular cardiomyopathy: Genetic characteristics.

Vischer AS, Castelletti S, Syrris P, McKenna WJ, Pantazis A. Vischer AS, et al. Among authors: pantazis a. Int J Cardiol. 2019 Jul 1;286:99-103. doi: 10.1016/j.ijcard.2019.01.065. Epub 2019 Jan 27. Int J Cardiol. 2019. PMID: 30765282

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