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Page 1
Long-term prognosis of patients with an SCN5A loss-of-function variant and progressive cardiac conduction disorder or Brugada syndrome.
Tuijnenburg F, Proost VM, Thollet A, Barc J, Groffen AJA, Veerman CC, van der Crabben SN, van der Pas VR, Kyndt F, Jurgens SJ, Tanck MWT, Postema PG, Peter van Tintelen J, Bezzina CR, Probst V, Wilde AAM, Gourraud JB, Amin AS. Tuijnenburg F, et al. Among authors: thollet a. Heart Rhythm. 2024 Nov 2:S1547-5271(24)03518-5. doi: 10.1016/j.hrthm.2024.10.057. Online ahead of print. Heart Rhythm. 2024. PMID: 39491571 Free article.
Prognostic significance of fever-induced Brugada syndrome.
Mizusawa Y, Morita H, Adler A, Havakuk O, Thollet A, Maury P, Wang DW, Hong K, Gandjbakhch E, Sacher F, Hu D, Amin AS, Lahrouchi N, Tan HL, Antzelevitch C, Probst V, Viskin S, Wilde AA. Mizusawa Y, et al. Among authors: thollet a. Heart Rhythm. 2016 Jul;13(7):1515-20. doi: 10.1016/j.hrthm.2016.03.044. Epub 2016 Mar 23. Heart Rhythm. 2016. PMID: 27033637
Sodium-channel blocker challenge in the familial screening of Brugada syndrome: Safety and predictors of positivity.
Therasse D, Sacher F, Petit B, Babuty D, Mabo P, Martins R, Jesel L, Maury P, Pasquie JL, Mansourati J, Dupuis JM, Kyndt F, Thollet A, Guyomarch B, Barc J, Schott JJ, Le Marec H, Redon R, Probst V, Gourraud JB. Therasse D, et al. Among authors: thollet a. Heart Rhythm. 2017 Oct;14(10):1442-1448. doi: 10.1016/j.hrthm.2017.06.031. Epub 2017 Jun 27. Heart Rhythm. 2017. PMID: 28666944
The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance.
Gourraud JB, Barc J, Thollet A, Le Scouarnec S, Le Marec H, Schott JJ, Redon R, Probst V. Gourraud JB, et al. Among authors: thollet a. Front Cardiovasc Med. 2016 Apr 25;3:9. doi: 10.3389/fcvm.2016.00009. eCollection 2016. Front Cardiovasc Med. 2016. PMID: 27200363 Free PMC article. Review.
Brugada syndrome: Diagnosis, risk stratification and management.
Gourraud JB, Barc J, Thollet A, Le Marec H, Probst V. Gourraud JB, et al. Among authors: thollet a. Arch Cardiovasc Dis. 2017 Mar;110(3):188-195. doi: 10.1016/j.acvd.2016.09.009. Epub 2017 Jan 27. Arch Cardiovasc Dis. 2017. PMID: 28139454 Free article. Review.
Clinical presentation and follow-up of women affected by Brugada syndrome.
Berthome P, Tixier R, Briand J, Geoffroy O, Babuty D, Mansourati J, Jesel L, Dupuis JM, Bru P, Kyndt F, Guyomarch B, Thollet A, Behar N, Mabo P, Sacher F, Probst V, Gourraud JB. Berthome P, et al. Among authors: thollet a. Heart Rhythm. 2019 Feb;16(2):260-267. doi: 10.1016/j.hrthm.2018.08.032. Epub 2018 Sep 5. Heart Rhythm. 2019. PMID: 30193851
Age at diagnosis of Brugada syndrome: Influence on clinical characteristics and risk of arrhythmia.
Minier M, Probst V, Berthome P, Tixier R, Briand J, Geoffroy O, Clementy N, Mansourati J, Jesel L, Dupuis JM, Bru P, Kyndt F, Guyomarch B, Thollet A, Behar N, Mabo P, Sacher F, Gourraud JB. Minier M, et al. Among authors: thollet a. Heart Rhythm. 2020 May;17(5 Pt A):743-749. doi: 10.1016/j.hrthm.2019.11.027. Epub 2019 Nov 29. Heart Rhythm. 2020. PMID: 31790831
Robustness and relevance of predictive score in sudden cardiac death for patients with Brugada syndrome.
Probst V, Goronflot T, Anys S, Tixier R, Briand J, Berthome P, Geoffroy O, Clementy N, Mansourati J, Jesel L, Dupuis JM, Bru P, Kyndt F, Wargny M, Guyomarch B, Thollet A, Mabo P, Gourraud PA, Behar N, Sacher F, Gourraud JB. Probst V, et al. Among authors: thollet a. Eur Heart J. 2021 May 1;42(17):1687-1695. doi: 10.1093/eurheartj/ehaa763. Eur Heart J. 2021. PMID: 33289793
Dose response to nadolol in congenital long QT syndrome.
Anys S, Arnaud M, Minois D, Rajalu A, Guyomarch B, Thollet A, Gourraud JB, Probst V. Anys S, et al. Among authors: thollet a. Heart Rhythm. 2021 Aug;18(8):1377-1383. doi: 10.1016/j.hrthm.2021.04.021. Epub 2021 Apr 24. Heart Rhythm. 2021. PMID: 33905813
Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility.
Barc J, Tadros R, Glinge C, Chiang DY, Jouni M, Simonet F, Jurgens SJ, Baudic M, Nicastro M, Potet F, Offerhaus JA, Walsh R, Choi SH, Verkerk AO, Mizusawa Y, Anys S, Minois D, Arnaud M, Duchateau J, Wijeyeratne YD, Muir A, Papadakis M, Castelletti S, Torchio M, Ortuño CG, Lacunza J, Giachino DF, Cerrato N, Martins RP, Campuzano O, Van Dooren S, Thollet A, Kyndt F, Mazzanti A, Clémenty N, Bisson A, Corveleyn A, Stallmeyer B, Dittmann S, Saenen J, Noël A, Honarbakhsh S, Rudic B, Marzak H, Rowe MK, Federspiel C, Le Page S, Placide L, Milhem A, Barajas-Martinez H, Beckmann BM, Krapels IP, Steinfurt J, Winkel BG, Jabbari R, Shoemaker MB, Boukens BJ, Škorić-Milosavljević D, Bikker H, Manevy F, Lichtner P, Ribasés M, Meitinger T, Müller-Nurasyid M; KORA-Study Group; Veldink JH, van den Berg LH, Van Damme P, Cusi D, Lanzani C, Rigade S, Charpentier E, Baron E, Bonnaud S, Lecointe S, Donnart A, Le Marec H, Chatel S, Karakachoff M, Bézieau S, London B, Tfelt-Hansen J, Roden D, Odening KE, Cerrone M, Chinitz LA, Volders PG, van de Berg MP, Laurent G, Faivre L, Antzelevitch C, Kääb S, Arnaout AA, Dupuis JM, Pasquie JL, Billon O, Roberts JD, Jesel L, Borggrefe M, Lambiase PD, Mansourati… See abstract for full author list ➔ Barc J, et al. Among authors: thollet a. Nat Genet. 2022 Mar;54(3):232-239. doi: 10.1038/s41588-021-01007-6. Epub 2022 Feb 24. Nat Genet. 2022. PMID: 35210625 Free PMC article.
31 results