Syrris P - Search Results

1

Phenotype and Clinical Outcomes in Desmin-Related Arrhythmogenic Cardiomyopathy.

Bermudez-Jimenez FJ, Protonotarios A, García-Hernández S, Pérez Asensio A, Rampazzo A, Zorio E, Brodehl A, Arias MA, Macías-Ruiz R, Fernández-Armenta J, Remior Perez P, Muñoz-Esparza C, Pilichou K, Bauce B, Merino JL, Moliner-Abós C, Ochoa JP, Barriales-Villa R, Garcia-Pavia P, Lopes LR, Syrris P, Corrado D, Elliott PM, McKenna WJ, Jimenez-Jaimez J. Bermudez-Jimenez FJ, et al. Among authors: syrris p. JACC Clin Electrophysiol. 2024 Jun;10(6):1178-1190. doi: 10.1016/j.jacep.2024.02.031. Epub 2024 May 8. JACC Clin Electrophysiol. 2024. PMID: 38727660

2

Non-enzymatic glycosylation of the dipeptide L-carnosine, a potential anti-protein-cross-linking agent.

Hipkiss AR, Michaelis J, Syrris P. Hipkiss AR, et al. Among authors: syrris p. FEBS Lett. 1995 Aug 28;371(1):81-5. doi: 10.1016/0014-5793(95)00849-5. FEBS Lett. 1995. PMID: 7664889 Free article.

3

Molecular analysis of Berardinelli-Seip congenital lipodystrophy in Oman: evidence for multiple loci.

Heathcote K, Rajab A, Magré J, Syrris P, Besti M, Patton M, Délépine M, Lathrop M, Capeau J, Jeffery S. Heathcote K, et al. Among authors: syrris p. Diabetes. 2002 Apr;51(4):1291-3. doi: 10.2337/diabetes.51.4.1291. Diabetes. 2002. PMID: 11916958

4

Novel TFAP2B mutation in nonsyndromic patent ductus arteriosus.

Khetyar M, Syrris P, Tinworth L, Abushaban L, Carter N. Khetyar M, et al. Among authors: syrris p. Genet Test. 2008 Sep;12(3):457-9. doi: 10.1089/gte.2008.0015. Genet Test. 2008. PMID: 18752453

5

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.

6

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.

7

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

8

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.

9

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.

10

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

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