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Page 1
Malignant response to ajmaline challenge in SCN5A mutation carriers: experience from a large familial study.
Gandjbakhch E, Fressart V, Duthoit G, Marquié C, Deharo JC, Pousset F, Hebert JL, Simon F, Himbert C, Klug D, Charron P, Hidden-Lucet F. Gandjbakhch E, et al. Among authors: charron p. Int J Cardiol. 2014 Mar 1;172(1):256-8. doi: 10.1016/j.ijcard.2013.12.269. Epub 2014 Jan 10. Int J Cardiol. 2014. PMID: 24476701 Free article. No abstract available.
[Genetics of inherited cardiomyopathies].
Richard P, Fressart V, Charron P, Hainque B. Richard P, et al. Among authors: charron p. Pathol Biol (Paris). 2010 Oct;58(5):343-52. doi: 10.1016/j.patbio.2009.10.010. Epub 2009 Nov 25. Pathol Biol (Paris). 2010. PMID: 19942368 Review. French.
Association between common cardiovascular risk factors and clinical phenotype in patients with hypertrophic cardiomyopathy from the European Society of Cardiology (ESC) EurObservational Research Programme (EORP) Cardiomyopathy/Myocarditis registry.
Lopes LR, Losi MA, Sheikh N, Laroche C, Charron P, Gimeno J, Kaski JP, Maggioni AP, Tavazzi L, Arbustini E, Brito D, Celutkiene J, Hagege A, Linhart A, Mogensen J, Garcia-Pinilla JM, Ripoll-Vera T, Seggewiss H, Villacorta E, Caforio A, Elliott PM; Cardiomyopathy Registry Investigators Group. Lopes LR, et al. Among authors: charron p. Eur Heart J Qual Care Clin Outcomes. 2022 Dec 13;9(1):42-53. doi: 10.1093/ehjqcco/qcac006. Eur Heart J Qual Care Clin Outcomes. 2022. PMID: 35138368 Free PMC article.
Penetrance of familial hypertrophic cardiomyopathy.
Charron P, Carrier L, Dubourg O, Tesson F, Desnos M, Richard P, Bonne G, Guicheney P, Hainque B, Bouhour JB, Mallet A, Feingold J, Schwartz K, Komajda M. Charron P, et al. Genet Couns. 1997;8(2):107-14. Genet Couns. 1997. PMID: 9219008
247 results