Syrris P - Search Results

1

Desmoplakin missense and non-missense mutations in arrhythmogenic right ventricular cardiomyopathy: Genotype-phenotype correlation.

Castelletti S, Vischer AS, Syrris P, Crotti L, Spazzolini C, Ghidoni A, Parati G, Jenkins S, Kotta MC, McKenna WJ, Schwartz PJ, Pantazis A. Castelletti S, et al. Among authors: syrris p. Int J Cardiol. 2017 Dec 15;249:268-273. doi: 10.1016/j.ijcard.2017.05.018. Epub 2017 May 10. Int J Cardiol. 2017. PMID: 28527814

2

Cardiological assessment of first-degree relatives in sudden arrhythmic death syndrome.

Behr E, Wood DA, Wright M, Syrris P, Sheppard MN, Casey A, Davies MJ, McKenna W; Sudden Arrhythmic Death Syndrome Steering Group. Behr E, et al. Among authors: syrris p. Lancet. 2003 Nov 1;362(9394):1457-9. doi: 10.1016/s0140-6736(03)14692-2. Lancet. 2003. PMID: 14602442

3

Adenosine monophosphate-activated protein kinase disease mimicks hypertrophic cardiomyopathy and Wolff-Parkinson-White syndrome: natural history.

Murphy RT, Mogensen J, McGarry K, Bahl A, Evans A, Osman E, Syrris P, Gorman G, Farrell M, Holton JL, Hanna MG, Hughes S, Elliott PM, Macrae CA, McKenna WJ. Murphy RT, et al. Among authors: syrris p. J Am Coll Cardiol. 2005 Mar 15;45(6):922-30. doi: 10.1016/j.jacc.2004.11.053. J Am Coll Cardiol. 2005. PMID: 15766830 Free article.

4

Desmoplakin disease in arrhythmogenic right ventricular cardiomyopathy: early genotype-phenotype studies.

Sen-Chowdhry S, Syrris P, McKenna WJ. Sen-Chowdhry S, et al. Among authors: syrris p. Eur Heart J. 2005 Aug;26(16):1582-4. doi: 10.1093/eurheartj/ehi343. Epub 2005 Jun 7. Eur Heart J. 2005. PMID: 15941722 No abstract available.

5

Novel mutation in desmoplakin causes arrhythmogenic left ventricular cardiomyopathy.

Norman M, Simpson M, Mogensen J, Shaw A, Hughes S, Syrris P, Sen-Chowdhry S, Rowland E, Crosby A, McKenna WJ. Norman M, et al. Among authors: syrris p. Circulation. 2005 Aug 2;112(5):636-42. doi: 10.1161/CIRCULATIONAHA.104.532234. Circulation. 2005. PMID: 16061754

6

Genetics of right ventricular cardiomyopathy.

Sen-Chowdhry S, Syrris P, McKenna WJ. Sen-Chowdhry S, et al. Among authors: syrris p. J Cardiovasc Electrophysiol. 2005 Aug;16(8):927-35. doi: 10.1111/j.1540-8167.2005.40842.x. J Cardiovasc Electrophysiol. 2005. PMID: 16101641 Review.

7

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. Circulation. 2006 Jan 24;113(3):356-64. doi: 10.1161/CIRCULATIONAHA.105.561654. Epub 2006 Jan 16. Circulation. 2006. PMID: 16415378 Free article.

8

Mutation screening of the PTPN11 gene in hypertrophic cardiomyopathy.

Limongelli G, Hawkes L, Calabro R, McKenna WJ, Syrris P. Limongelli G, et al. Among authors: syrris p. Eur J Med Genet. 2006 Sep-Oct;49(5):426-30. doi: 10.1016/j.ejmg.2006.01.003. Epub 2006 Feb 3. Eur J Med Genet. 2006. PMID: 16488201

9

Arrhythmogenic right ventricular cardiomyopathy caused by deletions in plakophilin-2 and plakoglobin (Naxos disease) in families from Greece and Cyprus: genotype-phenotype relations, diagnostic features and prognosis.

Antoniades L, Tsatsopoulou A, Anastasakis A, Syrris P, Asimaki A, Panagiotakos D, Zambartas C, Stefanadis C, McKenna WJ, Protonotarios N. Antoniades L, et al. Among authors: syrris p. Eur Heart J. 2006 Sep;27(18):2208-16. doi: 10.1093/eurheartj/ehl184. Epub 2006 Aug 7. Eur Heart J. 2006. PMID: 16893920

10

Arrhythmogenic right ventricular dysplasia/cardiomyopathy associated with mutations in the desmosomal gene desmocollin-2.

Syrris P, Ward D, Evans A, Asimaki A, Gandjbakhch E, Sen-Chowdhry S, McKenna WJ. Syrris P, et al. Am J Hum Genet. 2006 Nov;79(5):978-84. doi: 10.1086/509122. Epub 2006 Sep 27. Am J Hum Genet. 2006. PMID: 17033975 Free PMC article.

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