Fressart V - Search Results

1

Inherited Cardiomyopathies Revealed by Clinically Suspected Myocarditis: Highlights From Genetic Testing.

Ader F, Surget E, Charron P, Redheuil A, Zouaghi A, Maltret A, Marijon E, Denjoy I, Hermida A, Fressart V, Gandjbakhch E. Ader F, et al. Among authors: fressart v. Circ Genom Precis Med. 2020 Aug;13(4):e002744. doi: 10.1161/CIRCGEN.119.002744. Epub 2020 Jun 10. Circ Genom Precis Med. 2020. PMID: 32522011 Review. No abstract available.

2

The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases.

Six I, Hermida JS, Huang H, Gouas L, Fressart V, Benammar N, Hainque B, Denjoy I, Chahine M, Guicheney P. Six I, et al. Among authors: fressart v. Europace. 2008 Jan;10(1):79-85. doi: 10.1093/europace/eum271. Epub 2007 Dec 21. Europace. 2008. PMID: 18156160

3

Sporadic arrhythmogenic right ventricular cardiomyopathy/dysplasia due to a de novo mutation.

Gandjbakhch E, Fressart V, Bertaux G, Faivre L, Simon F, Frank R, Fontaine G, Villard E, Coirault C, Hainque B, Charron P. Gandjbakhch E, et al. Among authors: fressart v. Europace. 2009 Mar;11(3):379-81. doi: 10.1093/europace/eun378. Epub 2009 Jan 16. Europace. 2009. PMID: 19151369

4

[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.

5

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

6

Plakophilin 2A is the dominant isoform in human heart tissue: consequences for the genetic screening of arrhythmogenic right ventricular cardiomyopathy.

Gandjbakhch E, Charron P, Fressart V, Lorin de la Grandmaison G, Simon F, Gary F, Vite A, Hainque B, Hidden-Lucet F, Komajda M, Villard E. Gandjbakhch E, et al. Among authors: fressart v. Heart. 2011 May;97(10):844-9. doi: 10.1136/hrt.2010.205880. Epub 2011 Mar 3. Heart. 2011. PMID: 21378009

7

Contraction delay of the RV outflow tract in patients with Brugada syndrome is dependent on the spontaneous ST-segment elevation pattern.

Rouzet F, Algalarrondo V, Burg S, Nassar P, Sarda-Mantel L, Aouate P, Frank R, Leenhardt A, Fressart V, Charron P, Slama MS, Le Guludec D. Rouzet F, et al. Among authors: fressart v. Heart Rhythm. 2011 Dec;8(12):1905-12. doi: 10.1016/j.hrthm.2011.07.026. Epub 2011 Jul 26. Heart Rhythm. 2011. PMID: 21798229

8

Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy.

Laurent G, Saal S, Amarouch MY, Béziau DM, Marsman RF, Faivre L, Barc J, Dina C, Bertaux G, Barthez O, Thauvin-Robinet C, Charron P, Fressart V, Maltret A, Villain E, Baron E, Mérot J, Turpault R, Coudière Y, Charpentier F, Schott JJ, Loussouarn G, Wilde AA, Wolf JE, Baró I, Kyndt F, Probst V. Laurent G, et al. Among authors: fressart v. J Am Coll Cardiol. 2012 Jul 10;60(2):144-56. doi: 10.1016/j.jacc.2012.02.052. J Am Coll Cardiol. 2012. PMID: 22766342 Free article.

9

Advising a cardiac disease gene positive yet phenotype negative or borderline abnormal athlete: is sporting disqualification really necessary?

Richard P, Denjoy I, Fressart V, Wilson MG, Carré F, Charron P. Richard P, et al. Among authors: fressart v. Br J Sports Med. 2012 Nov;46 Suppl 1:i59-68. doi: 10.1136/bjsports-2012-091318. Br J Sports Med. 2012. PMID: 23097481 Free article. Review.

10

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: fressart v. Front Physiol. 2012 Dec 27;3:474. doi: 10.3389/fphys.2012.00474. eCollection 2012. Front Physiol. 2012. PMID: 23293604 Free PMC article.

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