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Prevalence and Significance of Rare Genetic Variants in AKAP9 in Inherited Cardiac Diseases.
Hermida A, Ader F, Jedraszak G, Viboud G, Fressart V, Bréhin AC, Gérard M, Khraiche D, Palmyre A, Paziaud O, Popescu E, Proukhnitzky J, Laredo M, Richard P, Vedrenne G, Vernier A, Charron P, Gandjbakhch E. Hermida A, et al. Among authors: charron p. Circ Genom Precis Med. 2024 Feb;17(1):e004260. doi: 10.1161/CIRCGEN.123.004260. Epub 2024 Jan 23. Circ Genom Precis Med. 2024. PMID: 38258564 No abstract available.
Hypertrophic cardiomyopathy: distribution of disease genes, spectrum of mutations, and implications for a molecular diagnosis strategy.
Richard P, Charron P, Carrier L, Ledeuil C, Cheav T, Pichereau C, Benaiche A, Isnard R, Dubourg O, Burban M, Gueffet JP, Millaire A, Desnos M, Schwartz K, Hainque B, Komajda M; EUROGENE Heart Failure Project. Richard P, et al. Among authors: charron p. Circulation. 2003 May 6;107(17):2227-32. doi: 10.1161/01.CIR.0000066323.15244.54. Epub 2003 Apr 21. Circulation. 2003. PMID: 12707239
Brugada ECG pattern: a physiopathological prospective study based on clinical, electrophysiological, angiographic, and genetic findings.
Duthoit G, Fressart V, Hidden-Lucet F, Simon F, Kattygnarath D, Charron P, Himbert C, Aouate P, Guicheney P, Lecarpentier Y, Frank R, Hébert JL. Duthoit G, et al. Among authors: charron p. Front Physiol. 2012 Dec 27;3:474. doi: 10.3389/fphys.2012.00474. eCollection 2012. Front Physiol. 2012. PMID: 23293604 Free PMC article.
Desmosomal cadherins are decreased in explanted arrhythmogenic right ventricular dysplasia/cardiomyopathy patient hearts.
Vite A, Gandjbakhch E, Prost C, Fressart V, Fouret P, Neyroud N, Gary F, Donal E, Varnous S, Fontaine G, Fornes P, Hidden-Lucet F, Komajda M, Charron P, Villard E. Vite A, et al. Among authors: charron p. PLoS One. 2013 Sep 23;8(9):e75082. doi: 10.1371/journal.pone.0075082. eCollection 2013. PLoS One. 2013. PMID: 24086444 Free PMC article.
235 results