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541 results

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Page 1
Echocardiographic pitfalls in the diagnosis of hypertrophic cardiomyopathy.
Prasad K, Atherton J, Smith GC, McKenna WJ, Frenneaux MP, Nihoyannopoulos P. Prasad K, et al. Among authors: atherton j. Heart. 1999 Nov;82 Suppl 3(Suppl 3):III8-III15. doi: 10.1136/hrt.82.2008.iii8. Heart. 1999. PMID: 10534325 Free PMC article. No abstract available.
Establishment of an Australian National Genetic Heart Disease Registry.
Ingles J, McGaughran J, Vohra J, Weintraub RG, Davis A, Atherton J, Semsarian C. Ingles J, et al. Among authors: atherton j. Heart Lung Circ. 2008 Dec;17(6):463-7. doi: 10.1016/j.hlc.2008.05.603. Epub 2008 Aug 21. Heart Lung Circ. 2008. PMID: 18722159
Randomised controlled trial of a secondary prevention program for myocardial infarction patients ('ProActive Heart'): study protocol. Secondary prevention program for myocardial infarction patients.
Hawkes AL, Atherton J, Taylor CB, Scuffham P, Eadie K, Miller NH, Oldenburg B. Hawkes AL, et al. Among authors: atherton j. BMC Cardiovasc Disord. 2009 May 9;9:16. doi: 10.1186/1471-2261-9-16. BMC Cardiovasc Disord. 2009. PMID: 19426524 Free PMC article. Clinical Trial.
Exercise training in recently hospitalized heart failure patients enrolled in a disease management programme: design of the EJECTION-HF randomized controlled trial.
Mudge AM, Denaro CP, Scott AC, Atherton JJ, Meyers DE, Marwick TH, Adsett JA, Mullins RW, Suna JM, Scuffham PA, O'Rourke PK. Mudge AM, et al. Among authors: atherton jj. Eur J Heart Fail. 2011 Dec;13(12):1370-5. doi: 10.1093/eurjhf/hfr139. Epub 2011 Nov 6. Eur J Heart Fail. 2011. PMID: 22065870 Free article. Clinical Trial.
Clinical predictors of genetic testing outcomes in hypertrophic cardiomyopathy.
Ingles J, Sarina T, Yeates L, Hunt L, Macciocca I, McCormack L, Winship I, McGaughran J, Atherton J, Semsarian C. Ingles J, et al. Among authors: atherton j. Genet Med. 2013 Dec;15(12):972-7. doi: 10.1038/gim.2013.44. Epub 2013 Apr 18. Genet Med. 2013. PMID: 23598715 Free article.
Cardiac myosin-binding protein C gene mutation expressed as hypertrophic cardiomyopathy and left ventricular noncompaction within two families: insights from cardiac magnetic resonance in clinical screening: Camuglia MYBPC3 gene mutation and MRI.
Camuglia AC, Younger JF, McGaughran J, Lo A, Atherton JJ. Camuglia AC, et al. Among authors: atherton jj. Int J Cardiol. 2013 Oct 3;168(3):2950-2. doi: 10.1016/j.ijcard.2013.03.168. Epub 2013 Apr 30. Int J Cardiol. 2013. PMID: 23642604 No abstract available.
Antisense-mediated exon skipping: a therapeutic strategy for titin-based dilated cardiomyopathy.
Gramlich M, Pane LS, Zhou Q, Chen Z, Murgia M, Schötterl S, Goedel A, Metzger K, Brade T, Parrotta E, Schaller M, Gerull B, Thierfelder L, Aartsma-Rus A, Labeit S, Atherton JJ, McGaughran J, Harvey RP, Sinnecker D, Mann M, Laugwitz KL, Gawaz MP, Moretti A. Gramlich M, et al. Among authors: atherton jj. EMBO Mol Med. 2015 May;7(5):562-76. doi: 10.15252/emmm.201505047. EMBO Mol Med. 2015. PMID: 25759365 Free PMC article.
541 results