Kaski JP - Search Results

1

Penetrance of Hypertrophic Cardiomyopathy in Sarcomere Protein Mutation Carriers.

Lorenzini M, Norrish G, Field E, Ochoa JP, Cicerchia M, Akhtar MM, Syrris P, Lopes LR, Kaski JP, Elliott PM. Lorenzini M, et al. Among authors: kaski jp. J Am Coll Cardiol. 2020 Aug 4;76(5):550-559. doi: 10.1016/j.jacc.2020.06.011. J Am Coll Cardiol. 2020. PMID: 32731933 Free PMC article.

2

Outcomes after implantable cardioverter-defibrillator treatment in children with hypertrophic cardiomyopathy.

Kaski JP, Tomé Esteban MT, Lowe M, Sporton S, Rees P, Deanfield JE, McKenna WJ, Elliott PM. Kaski JP, et al. Heart. 2007 Mar;93(3):372-4. doi: 10.1136/hrt.2006.094730. Epub 2006 Aug 29. Heart. 2007. PMID: 16940391 Free PMC article. No abstract available.

3

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

4

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

5

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

6

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

7

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

8

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

9

Prevalence of sequence variants in the RAS-mitogen activated protein kinase signaling pathway in pre-adolescent children with hypertrophic cardiomyopathy.

Kaski JP, Syrris P, Shaw A, Alapi KZ, Cordeddu V, Esteban MT, Jenkins S, Ashworth M, Hammond P, Tartaglia M, McKenna WJ, Elliott PM. Kaski JP, et al. Circ Cardiovasc Genet. 2012 Jun;5(3):317-26. doi: 10.1161/CIRCGENETICS.111.960468. Epub 2012 May 15. Circ Cardiovasc Genet. 2012. PMID: 22589294

10

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.

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