Hidden-Lucet F - Search Results

1

Contribution of exome sequencing for genetic diagnostic in arrhythmogenic right ventricular cardiomyopathy/dysplasia.

Fedida J, Fressart V, Charron P, Surget E, Hery T, Richard P, Donal E, Keren B, Duthoit G, Hidden-Lucet F, Villard E, Gandjbakhch E. Fedida J, et al. PLoS One. 2017 Aug 2;12(8):e0181840. doi: 10.1371/journal.pone.0181840. eCollection 2017. PLoS One. 2017. PMID: 28767663 Free PMC article.

2

Brugada syndrome in pure black Africans.

Bonny A, Tonet J, Fontaine G, Lacotte J, Coignard E, Duthoit G, Hidden-Lucet F, Charron P, Brugada P, Frank R. Bonny A, et al. J Cardiovasc Electrophysiol. 2008 Apr;19(4):421-6. doi: 10.1111/j.1540-8167.2007.01041.x. Epub 2007 Dec 12. J Cardiovasc Electrophysiol. 2008. PMID: 18081762

3

Unusual pacemaker location due to pocket infection.

Moubarak G, Duthoit G, Hidden-Lucet F. Moubarak G, et al. Arch Cardiovasc Dis. 2009 Feb;102(2):155-6. doi: 10.1016/j.acvd.2008.08.014. Epub 2009 Jan 21. Arch Cardiovasc Dis. 2009. PMID: 19303584 Free article. No abstract available.

4

Percutaneous epicardial radiofrequency ablation of ventricular arrhythmias after failure of endocardial approach: a 9-year experience.

Grimard C, Lacotte J, Hidden-Lucet F, Duthoit G, Gallais Y, Frank R. Grimard C, et al. J Cardiovasc Electrophysiol. 2010 Jan;21(1):56-61. doi: 10.1111/j.1540-8167.2009.01544.x. Epub 2009 Jul 13. J Cardiovasc Electrophysiol. 2010. PMID: 19602023

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

Images in cardiovascular medicine. Fortuitous discovery of partial Uhl anomaly in a male adult.

Hébert JL, Duthoit G, Hidden-Lucet F, Cortès-Morichetti M, Bouchachi AA, Azarine A, Fressart V, Simon F, Le Guludec D, Lacotte J, Frank R, Lecarpentier Y. Hébert JL, et al. Circulation. 2010 Jun 8;121(22):e426-9. doi: 10.1161/CIRCULATIONAHA.110.960773. Circulation. 2010. PMID: 20530016 No abstract available.

7

A case for ambidextrous doctors.

Duthoit G, Frank R, Aouate P, Lacotte J, Hidden-Lucet F. Duthoit G, et al. Europace. 2010 Nov;12(11):1645-7. doi: 10.1093/europace/euq293. Epub 2010 Aug 2. Europace. 2010. PMID: 20682555

8

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. Heart. 2011 May;97(10):844-9. doi: 10.1136/hrt.2010.205880. Epub 2011 Mar 3. Heart. 2011. PMID: 21378009

9

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

10

Novel SCN5A mutations in two families with "Brugada-like" ST elevation in the inferior leads and conduction disturbances.

Maury P, Moreau A, Hidden-Lucet F, Leenhardt A, Fressart V, Berthet M, Denjoy I, Bennamar N, Rollin A, Cardin C, Guicheney P, Chahine M. Maury P, et al. J Interv Card Electrophysiol. 2013 Aug;37(2):131-40. doi: 10.1007/s10840-013-9805-7. Epub 2013 Apr 24. J Interv Card Electrophysiol. 2013. PMID: 23612926

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