Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

363 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.
Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. Among authors: probst v. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.
Clinical aspects and prognosis of Brugada syndrome in children.
Probst V, Denjoy I, Meregalli PG, Amirault JC, Sacher F, Mansourati J, Babuty D, Villain E, Victor J, Schott JJ, Lupoglazoff JM, Mabo P, Veltmann C, Jesel L, Chevalier P, Clur SA, Haissaguerre M, Wolpert C, Le Marec H, Wilde AA. Probst V, et al. Circulation. 2007 Apr 17;115(15):2042-8. doi: 10.1161/CIRCULATIONAHA.106.664219. Epub 2007 Apr 2. Circulation. 2007. PMID: 17404158
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
Watanabe H, Koopmann TT, Le Scouarnec S, Yang T, Ingram CR, Schott JJ, Demolombe S, Probst V, Anselme F, Escande D, Wiesfeld AC, Pfeufer A, Kääb S, Wichmann HE, Hasdemir C, Aizawa Y, Wilde AA, Roden DM, Bezzina CR. Watanabe H, et al. Among authors: probst v. J Clin Invest. 2008 Jun;118(6):2260-8. doi: 10.1172/JCI33891. J Clin Invest. 2008. PMID: 18464934 Free PMC article.
Are women with severely symptomatic brugada syndrome different from men?
Sacher F, Meregalli P, Veltmann C, Field ME, Solnon A, Bru P, Abbey S, Jaïs P, Tan HL, Wolpert C, Lande G, Bertault V, Derval N, Babuty D, Lacroix D, Boveda S, Maury P, Hocini M, Clémenty J, Mabo P, Lemarec H, Mansourati J, Borggrefe M, Wilde A, Haïssaguerre M, Probst V. Sacher F, et al. Among authors: probst v. J Cardiovasc Electrophysiol. 2008 Nov;19(11):1181-5. doi: 10.1111/j.1540-8167.2008.01223.x. Epub 2008 May 19. J Cardiovasc Electrophysiol. 2008. PMID: 18554195
SCN5A mutations and the role of genetic background in the pathophysiology of Brugada syndrome.
Probst V, Wilde AA, Barc J, Sacher F, Babuty D, Mabo P, Mansourati J, Le Scouarnec S, Kyndt F, Le Caignec C, Guicheney P, Gouas L, Albuisson J, Meregalli PG, Le Marec H, Tan HL, Schott JJ. Probst V, et al. Circ Cardiovasc Genet. 2009 Dec;2(6):552-7. doi: 10.1161/CIRCGENETICS.109.853374. Epub 2009 Sep 29. Circ Cardiovasc Genet. 2009. PMID: 20031634
363 results