Free Access
Med Sci (Paris)
Volume 20, Number 6-7, Juin-Juillet 2004
Page(s) 623 - 625
Section Le Magazine : Nouvelles
Published online 15 June 2004
  1. De Vreede-Swagemakers JJ, Gorgels AP, et al. Out-of-hospital cardiac arrest in the 1990’s: a population-based study in the Maastricht area on incidence, characteristics and survival. J Am Coll Cardiol 1997; 30 : 1500–5. [Google Scholar]
  2. Dessertenne F. La tachycardie ventriculaire à deux foyers opposés variables. Arch Mal Cœur 1966; 9 : 263–5. [Google Scholar]
  3. Mohler PJ, Schott JJ, Gramolini AO, et al. Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death. Nature 2003; 421 : 634–9. [Google Scholar]
  4. Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and sudden cardiac death: a distinct clinical and electrocardiographic syndrome. A multicenter report. J Am Coll Cardiol 1992; 20 : 1391–6. [Google Scholar]
  5. Wilde AA, Antzelevitch C, Borggrefe M, et al. Proposed diagnostic criteria for the Brugada syndrome : consensus report. Circulation 2002; 106 : 2514–9. [Google Scholar]
  6. Priori SG, Napolitano C, Tiso N, et al. Mutations in the cardiac ryanodine receptor gene (hRyR2) underlie catecholaminergic polymorphic ventricular tachycardia. Circulation 2001; 103 : 196–200. [Google Scholar]
  7. Lahat H, Pras E, Olender T, et al. A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel. Am J Hum Genet 2001; 69 : 1378–4. [Google Scholar]
  8. Danieli GA, Rampazzo A. Genetics of arrhythmogenic right ventricular cardiomyopathy. Curr Opin Cardiol 2002; 17 : 218–21. [Google Scholar]
  9. Roberts R, Schwartz K. Myocardial diseases. Circulation 2000; 102 (suppl 4) : IV3 4–9. [Google Scholar]
  10. Javadpour MM, Tardiff JC, Pinz I, et al. Decreased energetics in murine hearts bearing the R92Q mutation in cardiac troponin T. J Clin Invest 2003; 11 : 768–75. [Google Scholar]
  11. Morgan CM, Gray KE, Robb GH. A survey of familial heart block. Br Heart J 1974; 36 : 693–6. [Google Scholar]
  12. Brink PA, Ferreira A, Moolman JC, et al. Gene for progressive familial heart block type I maps to chromosome 19q13. Circulation 1995; 91 : 1633–40. [Google Scholar]
  13. Schott JJ, Alshinawi C, Kyndt F, et al. Cardiac conduction defects associate with mutations in SCN5A. Nat Genet 1999; 23 : 20–1. [Google Scholar]
  14. Probst V, Kyndt F, Potet F, et al. Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenegre disease. J Am Coll Cardiol 2003; 41 : 643–52. [Google Scholar]
  15. Bezzina C, Veldkamp MW, van Den Berg MP, et al. A single Na(+) channel mutation causing both long-QT and Brugada syndromes. Circ Res 1999; 85 : 1206–13. [Google Scholar]
  16. Kyndt F, Probst V, Potet F, et al. Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family. Circulation 2001; 104 : 3081–6. [Google Scholar]
  17. Grant AO, Carboni MP, Neplioueva V, et al. Long QT syndrome, Brugada syndrome, and conduction system disease are linked to a single sodium channel mutation. J Clin Invest 2002; 110 : 1201–9. [Google Scholar]
  18. Chen YH, Xu SJ, Bendahhou S, et al. KCNQ1 gain-of-function mutation in familial atrial fibrillation. Science 2003; 299 : 251–4. [Google Scholar]

Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.

Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.

Initial download of the metrics may take a while.