Elliott PM - Search Results

1

Left ventricular hypertrophy caused by a novel nonsense mutation in FHL1.

Gossios TD, Lopes LR, Elliott PM. Gossios TD, et al. Among authors: elliott pm. Eur J Med Genet. 2013 May;56(5):251-5. doi: 10.1016/j.ejmg.2013.03.001. Epub 2013 Mar 14. Eur J Med Genet. 2013. PMID: 23500067

2

Progressive left ventricular remodeling in patients with hypertrophic cardiomyopathy and severe left ventricular hypertrophy.

Thaman R, Gimeno JR, Reith S, Esteban MT, Limongelli G, Murphy RT, Mist B, McKenna WJ, Elliott PM. Thaman R, et al. Among authors: elliott pm. J Am Coll Cardiol. 2004 Jul 21;44(2):398-405. doi: 10.1016/j.jacc.2004.01.054. J Am Coll Cardiol. 2004. PMID: 15261938 Free article.

3

Natural history and familial characteristics of isolated left ventricular non-compaction.

Murphy RT, Thaman R, Blanes JG, Ward D, Sevdalis E, Papra E, Kiotsekoglou A, Tome MT, Pellerin D, McKenna WJ, Elliott PM. Murphy RT, et al. Among authors: elliott pm. Eur Heart J. 2005 Jan;26(2):187-92. doi: 10.1093/eurheartj/ehi025. Epub 2004 Nov 30. Eur Heart J. 2005. PMID: 15618076

4

Left ventricular outflow tract obstruction and sudden death risk in patients with hypertrophic cardiomyopathy.

Elliott PM, Gimeno JR, Tomé MT, Shah J, Ward D, Thaman R, Mogensen J, McKenna WJ. Elliott PM, et al. Eur Heart J. 2006 Aug;27(16):1933-41. doi: 10.1093/eurheartj/ehl041. Epub 2006 Jun 5. Eur Heart J. 2006. PMID: 16754630

5

Acute myocardial ischemia associated with latent left ventricular outflow tract obstruction in the absence of left ventricular hypertrophy.

Page SP, Pantazis A, Elliott PM. Page SP, et al. Among authors: elliott pm. J Am Soc Echocardiogr. 2007 Jun;20(6):772.e1-4. doi: 10.1016/j.echo.2006.11.028. J Am Soc Echocardiogr. 2007. PMID: 17543754

6

Left ventricular noncompaction.

Pantazis AA, Elliott PM. Pantazis AA, et al. Among authors: elliott pm. Curr Opin Cardiol. 2009 May;24(3):209-13. doi: 10.1097/HCO.0b013e32832a11e7. Curr Opin Cardiol. 2009. PMID: 19318934 Review.

7

Long-term outcomes in hypertrophic cardiomyopathy caused by mutations in the cardiac troponin T gene.

Pasquale F, Syrris P, Kaski JP, Mogensen J, McKenna WJ, Elliott P. Pasquale F, et al. Circ Cardiovasc Genet. 2012 Feb 1;5(1):10-7. doi: 10.1161/CIRCGENETICS.111.959973. Epub 2011 Dec 5. Circ Cardiovasc Genet. 2012. PMID: 22144547

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: elliott pm. 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

Genetics of heart failure.

Lopes LR, Elliott PM. Lopes LR, et al. Among authors: elliott pm. Biochim Biophys Acta. 2013 Dec;1832(12):2451-61. doi: 10.1016/j.bbadis.2012.12.012. Epub 2013 Jan 6. Biochim Biophys Acta. 2013. PMID: 23298545 Free article. Review.

10

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing.

Lopes LR, Zekavati A, Syrris P, Hubank M, Giambartolomei C, Dalageorgou C, Jenkins S, McKenna W; Uk10k Consortium; Plagnol V, Elliott PM. Lopes LR, et al. Among authors: elliott pm. J Med Genet. 2013 Apr;50(4):228-39. doi: 10.1136/jmedgenet-2012-101270. Epub 2013 Feb 8. J Med Genet. 2013. PMID: 23396983 Free PMC article.

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