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Loss-of-function desmoplakin I and II mutations underlie dominant arrhythmogenic cardiomyopathy with a hair and skin phenotype.
Maruthappu T, Posafalvi A, Castelletti S, Delaney PJ, Syrris P, O'Toole EA, Green KJ, Elliott PM, Lambiase PD, Tinker A, McKenna WJ, Kelsell DP. Maruthappu T, et al. Among authors: mckenna wj. Br J Dermatol. 2019 May;180(5):1114-1122. doi: 10.1111/bjd.17388. Epub 2019 Jan 2. Br J Dermatol. 2019. PMID: 30382575 Free PMC article.
Familial dilated cardiomyopathy in the United Kingdom.
Keeling PJ, Gang Y, Smith G, Seo H, Bent SE, Murday V, Caforio AL, McKenna WJ. Keeling PJ, et al. Among authors: mckenna wj. Br Heart J. 1995 May;73(5):417-21. doi: 10.1136/hrt.73.5.417. Br Heart J. 1995. PMID: 7786655 Free PMC article.
Management of hypertrophic cardiomyopathy.
Elliott PM, McKenna WJ. Elliott PM, et al. Among authors: mckenna wj. Br J Hosp Med. 1996 Apr 3-16;55(7):419-23. Br J Hosp Med. 1996. PMID: 8730566 Review. No abstract available.
640 results