Rodriguez-Lafrasse C - Search Results

1

Spatiotemporal electrocardiographic characterization of ventricular depolarization and repolarization abnormalities in long QT syndrome.

Restier-Miron L, Fayn J, Millat G, Denjoy I, Rodriguez-Lafrasse C, Rubel P, Chevalier P. Restier-Miron L, et al. J Electrocardiol. 2007 Oct;40(4):368-74. doi: 10.1016/j.jelectrocard.2006.12.014. Epub 2007 Feb 20. J Electrocardiol. 2007. PMID: 17316676

2

Contribution of long-QT syndrome genetic variants in sudden infant death syndrome.

Millat G, Kugener B, Chevalier P, Chahine M, Huang H, Malicier D, Rodriguez-Lafrasse C, Rousson R. Millat G, et al. Pediatr Cardiol. 2009 May;30(4):502-9. doi: 10.1007/s00246-009-9417-2. Epub 2009 Mar 26. Pediatr Cardiol. 2009. PMID: 19322600

3

Spectrum of pathogenic mutations and associated polymorphisms in a cohort of 44 unrelated patients with long QT syndrome.

Millat G, Chevalier P, Restier-Miron L, Da Costa A, Bouvagnet P, Kugener B, Fayol L, Gonzàlez Armengod C, Oddou B, Chanavat V, Froidefond E, Perraudin R, Rousson R, Rodriguez-Lafrasse C. Millat G, et al. Clin Genet. 2006 Sep;70(3):214-27. doi: 10.1111/j.1399-0004.2006.00671.x. Clin Genet. 2006. PMID: 16922724

4

[Long QT syndrome in children: analysis of the Lyon series].

Iraqi M, Chevalier P, Raboisson MJ, Bozio A, Bouvagnet P, Millat G, Rodriguez-Lafrasse C. Iraqi M, et al. Arch Mal Coeur Vaiss. 2006 Feb;99(2):134-40. Arch Mal Coeur Vaiss. 2006. PMID: 16555697 French.

5

A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope.

Christé G, Thériault O, Chahine M, Millat G, Rodriguez-Lafrasse C, Rousson R, Deschênes I, Ficker E, Chevalier P. Christé G, et al. Heart Rhythm. 2008 Nov;5(11):1577-86. doi: 10.1016/j.hrthm.2008.08.031. Epub 2008 Aug 31. Heart Rhythm. 2008. PMID: 18984536 Free PMC article.

6

Biophysical characterization of a new SCN5A mutation S1333Y in a SIDS infant linked to long QT syndrome.

Huang H, Millat G, Rodriguez-Lafrasse C, Rousson R, Kugener B, Chevalier P, Chahine M. Huang H, et al. FEBS Lett. 2009 Mar 4;583(5):890-6. doi: 10.1016/j.febslet.2009.02.007. Epub 2009 Feb 10. FEBS Lett. 2009. PMID: 19302788 Free article.

7

Rapid, sensitive and inexpensive detection of SCN5A genetic variations by high resolution melting analysis.

Millat G, Chanavat V, Rodriguez-Lafrasse C, Rousson R. Millat G, et al. Clin Biochem. 2009 Apr;42(6):491-9. doi: 10.1016/j.clinbiochem.2008.10.014. Epub 2008 Nov 6. Clin Biochem. 2009. PMID: 19026623

8

Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition.

Chevalier P, Bellocq C, Millat G, Piqueras E, Potet F, Schott JJ, Baró I, Lemarec H, Barhanin J, Rousson R, Rodriguez-Lafrasse C. Chevalier P, et al. Heart Rhythm. 2007 Feb;4(2):170-4. doi: 10.1016/j.hrthm.2006.10.004. Epub 2006 Oct 13. Heart Rhythm. 2007. PMID: 17275752

9

Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy.

Millat G, Bouvagnet P, Chevalier P, Dauphin C, Jouk PS, Da Costa A, Prieur F, Bresson JL, Faivre L, Eicher JC, Chassaing N, Crehalet H, Porcher R, Rodriguez-Lafrasse C, Rousson R. Millat G, et al. Eur J Med Genet. 2010 Sep-Oct;53(5):261-7. doi: 10.1016/j.ejmg.2010.07.007. Epub 2010 Jul 30. Eur J Med Genet. 2010. PMID: 20624503

10

[Cardiac troponin I and C: analytical comparison and clinical-biological interpretation of three troponins assays].

Bionda C, Pettazzoni M, Rodriguez-Lafrasse C, Ardail D, Rousson R. Bionda C, et al. Ann Biol Clin (Paris). 2005 Mar-Apr;63(2):185-92. Ann Biol Clin (Paris). 2005. PMID: 15771976 Free article. French.

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