Roques, C., Fromes, Y., Fattal, E. :
Hydrosoluble polymers for muscular gene delivery
Eur J Pharm Biopharm, 2009 ; 72 (2) : 378-90
Publications (1184)
Barthelemy, I., Barrey, E., Thibaud, J. L., Uriarte, A., Voit, T., Blot, S., Hogrel, J. Y. :
Gait analysis using accelerometry in dystrophin-deficient dogs Neuromuscul Disord, 2009 ; 19 : 788-796
Gait analysis using accelerometry in dystrophin-deficient dogs Neuromuscul Disord, 2009 ; 19 : 788-796
Dunand, M., Lobrinus, J. A., Jeannet, P. Y., Behin, A., Claeys, K. G., Selcen, D., Kuntzer, T. :
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy Neuromuscul Disord, 2009 ; 19 : 802
Confirmation that abnormal desmin accumulation and migration are due to a desmin gene mutation in a familial cardiomyopathy and distal myopathy Neuromuscul Disord, 2009 ; 19 : 802
Lescure, A., Rederstorff, M., Krol, A., Guicheney, P., Allamand, V. :
Selenoprotein function and muscle disease Biochim Biophys Acta, 2009 ; 1790 (11) : 1569-74
Selenoprotein function and muscle disease Biochim Biophys Acta, 2009 ; 1790 (11) : 1569-74
Michel-Pellegrino, V, Li, K, Hewson, D, Hogrel, J Y, DuchĂȘne, J :
Techniques dâĂ©valuation Ă domicile de la qualitĂ© de lâĂ©quilibre et de la force de prĂ©hension chez la personne ĂągĂ©e en perte dâautonomie IRBM, 2009 ; 30 : 262-267
Techniques dâĂ©valuation Ă domicile de la qualitĂ© de lâĂ©quilibre et de la force de prĂ©hension chez la personne ĂągĂ©e en perte dâautonomie IRBM, 2009 ; 30 : 262-267
Vignier, N., Schlossarek, S., Fraysse, B., Mearini, G., Kramer, E., Pointu, H., Mougenot, N., Guiard, J., Reimer, R., Hohenberg, H., Schwartz, K., Vernet, M., Eschenhagen, T., Carrier, L. :
Nonsense-Mediated mRNA Decay and Ubiquitin-Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice Circ Res, 2009 ; 105 (3) : 239-248
Nonsense-Mediated mRNA Decay and Ubiquitin-Proteasome System Regulate Cardiac Myosin-Binding Protein C Mutant Levels in Cardiomyopathic Mice Circ Res, 2009 ; 105 (3) : 239-248
Burdi, R., Rolland, J. F., Fraysse, B., Litvinova, K., Cozzoli, A., Giannuzzi, V., Liantonio, A., Camerino, G. M., Sblendorio, V., Capogrosso, R. F., Palmieri, B., Andreetta, F., Confalonieri, P., De Benedictis, L., Montagnani, M., De Luca, A. :
Multiple pathological events in exercised dystrophic mdx mice are targeted by pentoxifylline: outcome of a large array of in vivo and ex vivo tests J Appl Physiol, 2009 ; 106 (4) : 1311-24
Multiple pathological events in exercised dystrophic mdx mice are targeted by pentoxifylline: outcome of a large array of in vivo and ex vivo tests J Appl Physiol, 2009 ; 106 (4) : 1311-24
Gargiulo, M., Lejeune, S., Tanguy, M. L., Lahlou-Laforet, K., Faudet, A., Cohen, D., Feingold, J., Durr, A. :
Long-term outcome of presymptomatic testing in Huntington disease Eur J Hum Genet, 2009 ; 17 (2) : 165-71
Long-term outcome of presymptomatic testing in Huntington disease Eur J Hum Genet, 2009 ; 17 (2) : 165-71
Outteryck, O., Richard, P., Lacour, A., Fournier, E., Zephir, H., Gaudon, K., Eymard, B., Hantai, D., Vermersch, P., Stojkovic, T. :
Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome J Neurol Neurosurg Psychiatry, 2009 ; 80 (4) : 450-1
Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome J Neurol Neurosurg Psychiatry, 2009 ; 80 (4) : 450-1
Daoud, F., Angeard, N., Demerre, B., Martie, I., Benyaou, R., Leturcq, F., Cossee, M., Saillour, Y., Tuffery, S., Urtizberea, A., Toutain, A., Echenne, B., Frischman, M., Mayer, M., Desguerre, I., Estournet, B., Reveillere, C., Penisson, Besnier, Cuisset, J. M., Kaplan, J. C., Heron, D., Rivier, F., Chelly, J. :
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression Hum Mol Genet, 2009 ; 18 (20) : 3779-3794
Analysis of Dp71 contribution in the severity of mental retardation through comparison of Duchenne and Becker patients differing by mutation consequences on Dp71 expression Hum Mol Genet, 2009 ; 18 (20) : 3779-3794
