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Page 1
[Neonatal forms of congenital long QT syndrome].
Lupoglazoff JM, Denjoy I, Villain E, Fressart V, Legall-Petit I, Bozio A, Berthet M, Benammar N, Hainque B, Guicheney P. Lupoglazoff JM, et al. Among authors: fressart v. Arch Mal Coeur Vaiss. 2004 May;97(5):479-83. Arch Mal Coeur Vaiss. 2004. PMID: 15214551 French.
Female predominance and transmission distortion in the long-QT syndrome.
Imboden M, Swan H, Denjoy I, Van Langen IM, Latinen-Forsblom PJ, Napolitano C, Fressart V, Breithardt G, Berthet M, Priori S, Hainque B, Wilde AA, Schulze-Bahr E, Feingold J, Guicheney P. Imboden M, et al. Among authors: fressart v. N Engl J Med. 2006 Dec 28;355(26):2744-51. doi: 10.1056/NEJMoa042786. N Engl J Med. 2006. PMID: 17192539 Free article.
[Genetics of inherited cardiomyopathies].
Richard P, Fressart V, Charron P, Hainque B. Richard P, et al. Among authors: fressart v. 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.
Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice.
Fressart V, Duthoit G, Donal E, Probst V, Deharo JC, Chevalier P, Klug D, Dubourg O, Delacretaz E, Cosnay P, Scanu P, Extramiana F, Keller D, Hidden-Lucet F, Simon F, Bessirard V, Roux-Buisson N, Hebert JL, Azarine A, Casset-Senon D, Rouzet F, Lecarpentier Y, Fontaine G, Coirault C, Frank R, Hainque B, Charron P. Fressart V, et al. Europace. 2010 Jun;12(6):861-8. doi: 10.1093/europace/euq104. Epub 2010 Apr 16. Europace. 2010. PMID: 20400443
MOG1: a new susceptibility gene for Brugada syndrome.
Kattygnarath D, Maugenre S, Neyroud N, Balse E, Ichai C, Denjoy I, Dilanian G, Martins RP, Fressart V, Berthet M, Schott JJ, Leenhardt A, Probst V, Le Marec H, Hainque B, Coulombe A, Hatem SN, Guicheney P. Kattygnarath D, et al. Among authors: fressart v. Circ Cardiovasc Genet. 2011 Jun;4(3):261-8. doi: 10.1161/CIRCGENETICS.110.959130. Epub 2011 Mar 29. Circ Cardiovasc Genet. 2011. PMID: 21447824
62 results