Collins, C. A., Gnocchi, V. F., White, R. B., Boldrin, L., Perez-Ruiz, A., Relaix, F., Morgan, J. E., Zammit, P. S. :
Integrated functions of Pax3 and Pax7 in the regulation of proliferation, cell size and myogenic differentiation
PLoS ONE, 2009 ; 4 (2) : e4475
Publications (1184)
Huze, C., Bauche, S., Richard, P., Chevessier, F., Goillot, E., Gaudon, K., Ben Ammar, A., Chaboud, A., Grosjean, I., Lecuyer, H. A., Bernard, V., Rouche, A., Alexandri, N., Kuntzer, T., Fardeau, M., Fournier, E., Brancaccio, A., Ruegg, M. A., Koenig, J., Eymard, B., Schaeffer, L., Hantai, D. :
Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function Am J Hum Genet, 2009 ; 85 (2) : 155-167
Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function Am J Hum Genet, 2009 ; 85 (2) : 155-167
Orlikowski, D., Chevret, S., Quera-Salva, M. A., Laforet, P., Lofaso, F., Verschueren, A., Pouget, J., Eymard, B., Annane, D. :
Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: a multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trial Clin Ther, 2009 ; 31 (8) : 1765-73
Modafinil for the treatment of hypersomnia associated with myotonic muscular dystrophy in adults: a multicenter, prospective, randomized, double-blind, placebo-controlled, 4-week trial Clin Ther, 2009 ; 31 (8) : 1765-73
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
Roques, C., Fromes, Y., Fattal, E. :
Hydrosoluble polymers for muscular gene delivery Eur J Pharm Biopharm, 2009 ; 72 (2) : 378-90
Hydrosoluble polymers for muscular gene delivery Eur J Pharm Biopharm, 2009 ; 72 (2) : 378-90
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
Michel-Pellegrino, V, Li, K, Hewson, D, Hogrel, J Y, DuchĂŞne, J :
Techniques d’évaluation à domicile de la qualité de l’équilibre et de la force de préhension chez la personne âgée en perte d’autonomie IRBM, 2009 ; 30 : 262-267
Techniques d’évaluation à domicile de la qualité de l’équilibre et de la force de préhension chez la personne âgée en perte d’autonomie IRBM, 2009 ; 30 : 262-267
