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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. Among authors: schott jj. Circulation. 2007 Apr 17;115(15):2042-8. doi: 10.1161/CIRCULATIONAHA.106.664219. Epub 2007 Apr 2. Circulation. 2007. PMID: 17404158
[Hereditary cardiac arrhythmia].
Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Apr;90 Spec No 1:57-66. Arch Mal Coeur Vaiss. 1997. PMID: 9238458 Review. French.
[Congenital long QT syndromes].
Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Jun;90 Spec No 3:25-35. Arch Mal Coeur Vaiss. 1997. PMID: 9295920 French.
Cardiac conduction defects associate with mutations in SCN5A.
Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.
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: schott jj. 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.
143 results