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Position paper concerning the competence, performance and environment required for the practice of ablation in children and in congenital heart disease.
Maury P, Thambo JB, Maltret A, Combes N, Hascoet S, Derval N, Ladouceur M, Acar P, Amedro P, Anselm F, Bajolle F, Basquin A, Belli E, Bordachar P, Duthoit G, Di Filippo S, Fauchier L, Gandjbakhch E, Gras D, Gronier C, Karsenty C, Klug D, Koutbi L, Lacotte J, Laurent G, Laux D, Mansourati J, Marijon E, Ovaert C, Sacher F, Sadoul N, Taieb J, Waldmann V, Warinfresse K, Defaye P, Piot O, Boveda S; Working Group of Pacing, Electrophysiology of the French Society of Cardiology, the Affiliate Group of Paediatric, Adult Congenital Cardiology of the French Society of Cardiology. Maury P, et al. Among authors: maltret a. Arch Cardiovasc Dis. 2020 Aug-Sep;113(8-9):492-502. doi: 10.1016/j.acvd.2020.02.002. Epub 2020 May 24. Arch Cardiovasc Dis. 2020. PMID: 32461091 Free article. Review.
Correlation between AF substrate ablation difficulty and left atrial fibrosis quantified by delayed-enhancement cardiac magnetic resonance.
Seitz J, Horvilleur J, Lacotte J, O H-Ici D, Mouhoub Y, Maltret A, Salerno F, Mylotte D, Monchi M, Garot J. Seitz J, et al. Among authors: maltret a. Pacing Clin Electrophysiol. 2011 Oct;34(10):1267-77. doi: 10.1111/j.1540-8159.2011.03148.x. Epub 2011 Jun 8. Pacing Clin Electrophysiol. 2011. PMID: 21651593 Clinical Trial.
The role of stress test for predicting genetic mutations and future cardiac events in asymptomatic relatives of catecholaminergic polymorphic ventricular tachycardia probands.
Hayashi M, Denjoy I, Hayashi M, Extramiana F, Maltret A, Roux-Buisson N, Lupoglazoff JM, Klug D, Maury P, Messali A, Guicheney P, Leenhardt A. Hayashi M, et al. Among authors: maltret a. Europace. 2012 Sep;14(9):1344-51. doi: 10.1093/europace/eus031. Epub 2012 Mar 1. Europace. 2012. PMID: 22383456
A systematic variant screening in familial cases of congenital heart defects demonstrates the usefulness of molecular genetics in this field.
El Malti R, Liu H, Doray B, Thauvin C, Maltret A, Dauphin C, Gonçalves-Rocha M, Teboul M, Blanchet P, Roume J, Gronier C, Ducreux C, Veyrier M, Marçon F, Acar P, Lusson JR, Levy M, Beyler C, Vigneron J, Cordier-Alex MP, Heitz F, Sanlaville D, Bonnet D, Bouvagnet P. El Malti R, et al. Among authors: maltret a. Eur J Hum Genet. 2016 Feb;24(2):228-36. doi: 10.1038/ejhg.2015.105. Epub 2015 May 27. Eur J Hum Genet. 2016. PMID: 26014430 Free PMC article.
Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
Andorin A, Behr ER, Denjoy I, Crotti L, Dagradi F, Jesel L, Sacher F, Petit B, Mabo P, Maltret A, Wong LC, Degand B, Bertaux G, Maury P, Dulac Y, Delasalle B, Gourraud JB, Babuty D, Blom NA, Schwartz PJ, Wilde AA, Probst V. Andorin A, et al. Among authors: maltret a. Heart Rhythm. 2016 Jun;13(6):1274-82. doi: 10.1016/j.hrthm.2016.02.013. Epub 2016 Feb 24. Heart Rhythm. 2016. PMID: 26921764
Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene.
Maury P, Gandjbakhch E, Baruteau AE, Bessière F, Kyndt F, Bouvagnet P, Rollin A, Bonnet D, Probst V, Maltret A. Maury P, et al. Among authors: maltret a. J Am Coll Cardiol. 2016 Nov 29;68(21):2389-2390. doi: 10.1016/j.jacc.2016.08.064. J Am Coll Cardiol. 2016. PMID: 27884258 Free article. No abstract available.
66 results