Baligand, C., Vauchez, K., Fiszman, M., Vilquin, J. T., Carlier, P. G. :
Discrepancies between the fate of myoblast xenograft in mouse leg muscle and NMR label persistency after loading with Gd-DTPA or SPIOs
Gene Ther, 2009 ; 16 (6) : 734-745
Publications (1184)
Dumonceaux, J., Amthor, H. :
Current advances in the development of therapies for neuromuscular disorders based on myostatin signalling, 3rd International Institute of Myology Workshop, Paris, September 12th, 2008 Neuromuscul Disord, 2009 ; 19 (11) : 797-799
Current advances in the development of therapies for neuromuscular disorders based on myostatin signalling, 3rd International Institute of Myology Workshop, Paris, September 12th, 2008 Neuromuscul Disord, 2009 ; 19 (11) : 797-799
Lentschener, C., Gaujoux, S., Thillois, J. M., Duboc, D., Bertherat, J., Ozier, Y., Dousset, B. :
Increased arterial pressure is not predictive of haemodynamic instability in patients undergoing adrenalectomy for phaeochromocytoma Acta Anaesthesiol Scand, 2009 ; 53 (4) : 522-7
Increased arterial pressure is not predictive of haemodynamic instability in patients undergoing adrenalectomy for phaeochromocytoma Acta Anaesthesiol Scand, 2009 ; 53 (4) : 522-7
Roques, C., Fattal, E., Fromes, Y. :
Comparison of toxicity and transfection efficiency of amphiphilic block copolymers and polycationic polymers in striated muscles J Gene Med, 2009 ; 11 (3) : 240-9
Comparison of toxicity and transfection efficiency of amphiphilic block copolymers and polycationic polymers in striated muscles J Gene Med, 2009 ; 11 (3) : 240-9
Bourteel, H., Vermersch, P., Cuisset, J. M., Maurage, C. A., Laforet, P., Richard, P., Stojkovic, T. :
Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients J Neurol Neurosurg Psychiatry, 2009 ; 80 (12) : 1405-1408
Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patients J Neurol Neurosurg Psychiatry, 2009 ; 80 (12) : 1405-1408
Gargiulo, M :
Maladie neuromusculaire, prise en compte de la dimension psychologique Les Cahiers de Myologie, 2009 ; (1) : 23
Maladie neuromusculaire, prise en compte de la dimension psychologique Les Cahiers de Myologie, 2009 ; (1) : 23
Micallef, J., Attarian, S., Dubourg, O., Gonnaud, P. M., Hogrel, J. Y., Stojkovic, T., Bernard, R., Jouve, E., Pitel, S., Vacherot, F., Remec, J. F., Jomir, L., Azabou, E., Al-Moussawi, M., Lefebvre, M. N., Attolini, L., Yaici, S., Tanesse, D., Fontes, M., Pouget, J., Blin, O. :
Effect of ascorbic acid in patients with Charcot-Marie-Tooth disease type 1A: a multicentre, randomised, double-blind, placebo-controlled trial Lancet Neurol, 2009 ; 8 (12) : 1103-1110
Effect of ascorbic acid in patients with Charcot-Marie-Tooth disease type 1A: a multicentre, randomised, double-blind, placebo-controlled trial Lancet Neurol, 2009 ; 8 (12) : 1103-1110
Vauchez, K., Marolleau, J. P., Schmid, M., Khattar, P., Chapel, A., Catelain, C., Lecourt, S., Larghero, J., Fiszman, M., Vilquin, J. T. :
Aldehyde dehydrogenase activity identifies a population of human skeletal muscle cells with high myogenic capacities Mol Ther, 2009 ; 17 (11) : 1948-58
Aldehyde dehydrogenase activity identifies a population of human skeletal muscle cells with high myogenic capacities Mol Ther, 2009 ; 17 (11) : 1948-58
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
Integrated functions of Pax3 and Pax7 in the regulation of proliferation, cell size and myogenic differentiation PLoS ONE, 2009 ; 4 (2) : e4475
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
