14 results for author:"Chevalier P." in Literature citations
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| Molecular characterization of a large MYBPC3 rearrangement in a cohort of 100 unrelated patients with hypertrophic cardiomyopathy. Chanavat V., Seronde M.F., Bouvagnet P., Chevalier P., Rousson R., Millat G. Eur J Med Genet 55:163-166(2012) · Mapped (8) |
| Increased intracardiac vascular endothelial growth factor levels in patients with paroxysmal, but not persistent atrial fibrillation. Scridon A., Morel E., Nonin-Babary E., Girerd N., Fernandez C., Chevalier P. Europace 14:948-953(2012) · Mapped (7) |
| Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. Millat G., Bouvagnet P., Chevalier P., Sebbag L., Dulac A., Dauphin C., Jouk P.S., Delrue M.A., Thambo J.B., Le Metayer P. et al. Eur. J. Med. Genet. 54:E570-E575(2011) · UniProtKB (5) · Mapped (10) |
| Evidence for the role of horizontal transfer in generating pVT1, a large mosaic conjugative plasmid from the clam pathogen, Vibrio tapetis. Erauso G., Lakhal F., Bidault-Toffin A., Le Chevalier P., Bouloc P., Paillard C., Jacq A. PLoS ONE 6:e16759-e16759(2011) · UniProtKB (88) |
| Effect of cytochrome P450 2C19 genotype on voriconazole exposure in cystic fibrosis lung transplant patients. Berge M., Guillemain R., Tregouet D.A., Amrein C., Boussaud V., Chevalier P., Lillo-Lelouet A., Le Beller C., Laurent-Puig P., Beaune P.H. et al. Eur. J. Clin. Pharmacol. 67:253-260(2011) · Mapped (3) |
| Prevalence and spectrum of mutations in a cohort of 192 unrelated patients with hypertrophic cardiomyopathy. Millat G., Bouvagnet P., Chevalier P., Dauphin C., Jouk P.S., Da Costa A., Prieur F., Bresson J.L., Faivre L., Eicher J.C. et al. Eur J Med Genet 53:261-267(2010) · Mapped (23) |
| Desmosomal gene analysis in arrhythmogenic right ventricular dysplasia/cardiomyopathy: spectrum of mutations and clinical impact in practice. Fressart V., Duthoit G., Donal E., Probst V., Deharo J.C., Chevalier P., Klug D., Dubourg O., Delacretaz E., Cosnay P. et al. Europace 12:861-868(2010) · Mapped (10) |
| 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. Pediatr Cardiol 30:502-509(2009) · Mapped (37) |
| 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. |
| A new C-terminal hERG mutation A915fs+47X associated with symptomatic LQT2 and auditory-trigger syncope. Christe G., Theriault O., Chahine M., Millat G., Rodriguez-Lafrasse C., Rousson R., Deschenes I., Ficker E., Chevalier P. Heart Rhythm 5:1577-1586(2008) · Mapped (14) |
| Torsades de pointes complicating atrioventricular block: evidence for a genetic predisposition. Chevalier P., Bellocq C., Millat G., Piqueras E., Potet F., Schott J.J., Baro I., Lemarec H., Barhanin J., Rousson R. et al. Heart Rhythm 4:170-174(2007) · Mapped (37) |
| 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., Gonzalez Armengod C., Oddou B., Chanavat V. et al. Clin. Genet. 70:214-227(2006) · UniProtKB (3) |
| Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome. Neyroud N., Richard P., Vignier N., Donger C., Denjoy I., Demay L., Shkolnikova M., Pesce R., Chevalier P., Hainque B. et al. Circ. Res. 84:290-297(1999) · UniProtKB (1) |
| Purification, biochemical characterization and N-terminal sequence of a serine-protease with chymotrypsic and collagenolytic activities in a tropical shrimp, Penaeus vannamei (Crustacea, Decapoda). van Wormhoudt A., le Chevalier P., Sellos D. Comp. Biochem. Physiol. 103B:675-680(1992) · UniProtKB (2) |