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SCN5A overlap syndromes: An open-minded approach.
Porretta AP, Probst V, Bhuiyan ZA, Davoine E, Delinière A, Pascale P, Schlaepfer J, Superti-Furga A, Pruvot E. Porretta AP, et al. Among authors: probst v. Heart Rhythm. 2022 Aug;19(8):1363-1368. doi: 10.1016/j.hrthm.2022.03.1223. Epub 2022 Mar 26. Heart Rhythm. 2022. PMID: 35351625 Review.
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
Kapplinger JD, Tester DJ, Alders M, Benito B, Berthet M, Brugada J, Brugada P, Fressart V, Guerchicoff A, Harris-Kerr C, Kamakura S, Kyndt F, Koopmann TT, Miyamoto Y, Pfeiffer R, Pollevick GD, Probst V, Zumhagen S, Vatta M, Towbin JA, Shimizu W, Schulze-Bahr E, Antzelevitch C, Salisbury BA, Guicheney P, Wilde AA, Brugada R, Schott JJ, Ackerman MJ. Kapplinger JD, et al. Among authors: probst v. Heart Rhythm. 2010 Jan;7(1):33-46. doi: 10.1016/j.hrthm.2009.09.069. Epub 2009 Oct 8. Heart Rhythm. 2010. PMID: 20129283 Free PMC article.
Variable Na(v)1.5 protein expression from the wild-type allele correlates with the penetrance of cardiac conduction disease in the Scn5a(+/-) mouse model.
Leoni AL, Gavillet B, Rougier JS, Marionneau C, Probst V, Le Scouarnec S, Schott JJ, Demolombe S, Bruneval P, Huang CL, Colledge WH, Grace AA, Le Marec H, Wilde AA, Mohler PJ, Escande D, Abriel H, Charpentier F. Leoni AL, et al. Among authors: probst v. PLoS One. 2010 Feb 19;5(2):e9298. doi: 10.1371/journal.pone.0009298. PLoS One. 2010. PMID: 20174578 Free PMC article.
Prevalence and significance of rare RYR2 variants in arrhythmogenic right ventricular cardiomyopathy/dysplasia: results of a systematic screening.
Roux-Buisson N, Gandjbakhch E, Donal E, Probst V, Deharo JC, Chevalier P, Klug D, Mansencal N, Delacretaz E, Cosnay P, Scanu P, Extramiana F, Keller D, Hidden-Lucet F, Trapani J, Fouret P, Frank R, Fressart V, Fauré J, Lunardi J, Charron P. Roux-Buisson N, et al. Among authors: probst v. Heart Rhythm. 2014 Nov;11(11):1999-2009. doi: 10.1016/j.hrthm.2014.07.020. Epub 2014 Jul 17. Heart Rhythm. 2014. PMID: 25041964 Free article.
Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
Béziau DM, Barc J, O'Hara T, Le Gloan L, Amarouch MY, Solnon A, Pavin D, Lecointe S, Bouillet P, Gourraud JB, Guicheney P, Denjoy I, Redon R, Mabo P, le Marec H, Loussouarn G, Kyndt F, Schott JJ, Probst V, Baró I. Béziau DM, et al. Among authors: probst v. Basic Res Cardiol. 2014;109(6):446. doi: 10.1007/s00395-014-0446-5. Epub 2014 Oct 24. Basic Res Cardiol. 2014. PMID: 25341504
Increased Tpeak-Tend interval is highly and independently related to arrhythmic events in Brugada syndrome.
Maury P, Sacher F, Gourraud JB, Pasquié JL, Raczka F, Bongard V, Duparc A, Mondoly P, Sadron M, Chatel S, Derval N, Denis A, Cardin C, Davy JM, Hocini M, Jaïs P, Jesel L, Carrié D, Galinier M, Haïssaguerre M, Probst V, Rollin A. Maury P, et al. Among authors: probst v. Heart Rhythm. 2015 Dec;12(12):2469-76. doi: 10.1016/j.hrthm.2015.07.029. Epub 2015 Jul 21. Heart Rhythm. 2015. PMID: 26209263 Free article.
393 results