Kaski JP - Search Results

1

Endomyocardial biopsy: safety and prognostic utility in paediatric and adult myocarditis in the European Society of Cardiology EURObservational Research Programme Cardiomyopathy and Myocarditis Long-Term Registry.

Caforio ALP, Kaski JP, Gimeno JR, Elliott PM, Laroche C, Tavazzi L, Tendera M, Fu M, Sala S, Seferovic PM, Heliö T, Calò L, Blagova O, Amin A, Kindermann I, Sinagra G, Frustaci A, Bonnet D, Charron P, Maggioni AP; CMY Registry Investigators. Caforio ALP, et al. Among authors: kaski jp. Eur Heart J. 2024 Jul 21;45(28):2548-2569. doi: 10.1093/eurheartj/ehae169. Eur Heart J. 2024. PMID: 38594778

2

The classification concept of the ESC Working Group on myocardial and pericardial diseases for dilated cardiomyopathy.

Kaski JP, Elliott P; ESC Working Group. Kaski JP, et al. Herz. 2007 Sep;32(6):446-51. doi: 10.1007/s00059-007-3045-5. Herz. 2007. PMID: 17882369

3

Mutations in the cardiac Troponin C gene are a cause of idiopathic dilated cardiomyopathy in childhood.

Kaski JP, Burch M, Elliott PM. Kaski JP, et al. Cardiol Young. 2007 Dec;17(6):675-7. doi: 10.1017/S1047951107001291. Epub 2007 Nov 1. Cardiol Young. 2007. PMID: 17977476

4

B-type natriuretic peptide predicts disease severity in children with hypertrophic cardiomyopathy.

Kaski JP, Tomé-Esteban MT, Mead-Regan S, Pantazis A, Marek J, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Heart. 2008 Oct;94(10):1307-11. doi: 10.1136/hrt.2007.126748. Epub 2007 Dec 10. Heart. 2008. PMID: 18070943

5

Idiopathic restrictive cardiomyopathy in children is caused by mutations in cardiac sarcomere protein genes.

Kaski JP, Syrris P, Burch M, Tomé-Esteban MT, Fenton M, Christiansen M, Andersen PS, Sebire N, Ashworth M, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Heart. 2008 Nov;94(11):1478-84. doi: 10.1136/hrt.2007.134684. Epub 2008 May 8. Heart. 2008. PMID: 18467357

6

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. 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

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. Among authors: kaski jp. 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

Cardiomyopathy in children: importance of aetiology in prognosis.

Kaski JP, Limongelli G. Kaski JP, et al. Lancet. 2014 Mar 1;383(9919):781-2. doi: 10.1016/S0140-6736(14)60400-1. Lancet. 2014. PMID: 24581663 No abstract available.

9

Sudden arrhythmic death syndrome: diagnostic yield of comprehensive clinical evaluation of pediatric first-degree relatives.

Giudici V, Spanaki A, Hendry J, Mead-Regan S, Field E, Zuccotti GV, Abrams D, Lowe M, Kaski JP. Giudici V, et al. Among authors: kaski jp. Pacing Clin Electrophysiol. 2014 Dec;37(12):1681-5. doi: 10.1111/pace.12479. Epub 2014 Aug 19. Pacing Clin Electrophysiol. 2014. PMID: 25139444

10

High prevalence of early repolarization in the paediatric relatives of sudden arrhythmic death syndrome victims and in normal controls.

McCorquodale A, Poulton R, Hendry J, Norrish G, Field E, Mead-Regan S, Lowe M, Kaski JP. McCorquodale A, et al. Among authors: kaski jp. Europace. 2017 Aug 1;19(8):1385-1391. doi: 10.1093/europace/euw248. Europace. 2017. PMID: 27965319

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