Djouadi, F., Lecarpentier, Y., Hebert, J. L., Charron, P., Bastin, J., Coirault, C. :
A potential link between peroxisome proliferator-activated receptor signalling and the pathogenesis of arrhythmogenic right ventricular cardiomyopathy
Cardiovasc Res, 2009 ; 84 (1) : 83-90
Publications (1181)
Krahn, M., Borges, A., Navarro, C., Schuit, R., Stojkovic, T., Torrente, Y., Wein, N., Pecheux, C., Levy, N. :
Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR Genet Test Mol Biomarkers, 2009 ; 13 (4) : 439-442
Identification of Different Genomic Deletions and One Duplication in the Dysferlin Gene Using Multiplex Ligation-Dependent Probe Amplification and Genomic Quantitative PCR Genet Test Mol Biomarkers, 2009 ; 13 (4) : 439-442
Relaix, F., Marcelle, C. :
Muscle stem cells Curr Opin Cell Biol, 2009 ; 21 (6) : 748-53
Muscle stem cells Curr Opin Cell Biol, 2009 ; 21 (6) : 748-53
Bitoun, M., Durieux, A. C., Prudhon, B., Bevilacqua, J. A., Herledan, A., Sakanyan, V., Urtizberea, A., Cartier, L., Romero, N. B., Guicheney, P. :
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis Hum Mutat, 2009 ; 30 (10) : 1419-1427
Dynamin 2 mutations associated with human diseases impair clathrin-mediated receptor endocytosis Hum Mutat, 2009 ; 30 (10) : 1419-1427
Friedrich, F. W., Bausero, P., Sun, Y., Treszl, A., Kramer, E., Juhr, D., Richard, P., Wegscheider, K., Schwartz, K., Brito, D., Arbustini, E., Waldenstrom, A., Isnard, R., Komajda, M., Eschenhagen, T., Carrier, L. :
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy Eur Heart J, 2009 ; 30 (13) : 1648-55
A new polymorphism in human calmodulin III gene promoter is a potential modifier gene for familial hypertrophic cardiomyopathy Eur Heart J, 2009 ; 30 (13) : 1648-55
Marmursztejn, J., Vignaux, O., Cohen, P., Guilpain, P., Pagnoux, C., Gouya, H., Mouthon, L., Legmann, P., Duboc, D., Guillevin, L. :
Impact of cardiac magnetic resonance imaging for assessment of Churg-Strauss syndrome: a cross-sectional study in 20 patients Clin Exp Rheumatol, 2009 ; 27 (1 Suppl 52) : S70-6
Impact of cardiac magnetic resonance imaging for assessment of Churg-Strauss syndrome: a cross-sectional study in 20 patients Clin Exp Rheumatol, 2009 ; 27 (1 Suppl 52) : S70-6
Tuffery-Giraud, S, Béroud, C, Leturcq, F, Ben Yaou, R, Hamroun, D, Michel-Calemard, L, Moizard, M P, Bernard, R, Cossée, M, Boisseau, P, Blayau, M, Creveaux, I, Guiochon-Mantel, A, de Martinville, B, Philippe, C, Monnier, N, Bieth, E, Khau van Kien, P, Desmet, F O, Humbertclaude, V, Kaplan, J C, Chelly, J, Claustres, M :
Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase Human Mutation, 2009 ; 30 (934-945) :
Genotype-phenotype analysis in 2405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase Human Mutation, 2009 ; 30 (934-945) :
Claeys, K. G., Zuchner, S., Kennerson, M., Berciano, J., Garcia, A., Verhoeven, K., Storey, E., Merory, J. R., Bienfait, H. M., Lammens, M., Nelis, E., Baets, J., De Vriendt, E., Berneman, Z. N., De Veuster, I., Vance, J. M., Nicholson, G., Timmerman, V., De Jonghe, P. :
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy Brain, 2009 ; 132 (Pt 7) : 1741-52
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy Brain, 2009 ; 132 (Pt 7) : 1741-52
Hicks, D., Lampe, A. K., Laval, S. H., Allamand, V., Jimenez-Mallebrera, C., Walter, M. C., Muntoni, F., Quijano-Roy, S., Richard, P., Straub, V., Lochmuller, H., Bushby, K. M. :
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue Brain, 2009 ; 132 (Pt 1) : 147-55
Cyclosporine A treatment for Ullrich congenital muscular dystrophy: a cellular study of mitochondrial dysfunction and its rescue Brain, 2009 ; 132 (Pt 1) : 147-55
Muntoni, F., Guicheney, P., Voit, T. :
158th ENMC international workshop on congenital muscular dystrophy (Xth international CMD workshop) 8th-10th February 2008 Naarden, The Netherlands Neuromuscul Disord, 2009 ; 19 (3) : 229-34
158th ENMC international workshop on congenital muscular dystrophy (Xth international CMD workshop) 8th-10th February 2008 Naarden, The Netherlands Neuromuscul Disord, 2009 ; 19 (3) : 229-34
