Douillard-Guilloux, G., Raben, N., Takikita, S., Ferry, A., Vignaud, A., Guillet-Deniau, I., Favier, M., Thurberg, B. L., Roach, P. J., Caillaud, C., Richard, E. :
Restoration of muscle functionality by genetic suppression of glycogen synthesis in a murine model of Pompe disease
Hum Mol Genet, 2010 ; 19 (4) : 684-96
Publications (1184)
Lorain, S, Peccate, C, Le Hir, M, Garcia, L :
Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts PLoS ONE, 2010 ; 5 (5) : e10894
Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts PLoS ONE, 2010 ; 5 (5) : e10894
van der Ploeg, A. T., Clemens, P. R., Corzo, D., Escolar, D. M., Florence, J., Groeneveld, G. J., Herson, S., Kishnani, P. S., Laforet, P., Lake, S. L., Lange, D. J., Leshner, R. T., Mayhew, J. E., Morgan, C., Nozaki, K., Park, D. J., Pestronk, A., Rosenbloom, B., Skrinar, A., van Capelle, C. I., van der Beek, N. A., Wasserstein, M., Zivkovic, S. A. :
A randomized study of alglucosidase alfa in late-onset Pompe’s disease N Engl J Med, 2010 ; 362 (15) : 1396-406
A randomized study of alglucosidase alfa in late-onset Pompe’s disease N Engl J Med, 2010 ; 362 (15) : 1396-406
Ben Ammar, A., Petit, F., Alexandri, N., Gaudon, K., Bauche, S., Rouche, A., Gras, D., Fournier, E., Koenig, J., Stojkovic, T., Lacour, A., Petiot, P., Zagnoli, F., Viollet, L., Pellegrini, N., Orlikowski, D., Lazaro, L., Ferrer, X., Stoltenburg, G., Paturneau-Jouas, M., Hentati, F., Fardeau, M., Sternberg, D., Hantai, D., Richard, P., Eymard, B. :
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 J Neurol, 2010 ; 257 (5) : 754-766
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 J Neurol, 2010 ; 257 (5) : 754-766
Garcin, B., Lenglet, T., Dubourg, O., Mesnage, V., Levy, R. :
Dropped head syndrome as a presenting sign of scleromyositis J Neurol Sci, 2010 ; 292 (1-2) : 101-103
Dropped head syndrome as a presenting sign of scleromyositis J Neurol Sci, 2010 ; 292 (1-2) : 101-103
Muntoni, F., Voit, T :
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009 Neuromuscul Disord, 2010 ; 20 (5) : 355-62
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009 Neuromuscul Disord, 2010 ; 20 (5) : 355-62
Cavalcante, P., Barberis, M., Cannone, M., Baggi, F., Antozzi, C., Maggi, L., Cornelio, F., Barbi, M., Dido, P., Berrih-Aknin, S., Mantegazza, R., Bernasconi, P. :
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravis Neurology, 2010 ; 74 (14) : 1118-26
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravis Neurology, 2010 ; 74 (14) : 1118-26
Laforet, P., Doppler, V., Caillaud, C., Laloui, K., Claeys, K. G., Richard, P., Ferreiro, A., Eymard, B. :
Rigid spine syndrome revealing late-onset Pompe disease Neuromuscul Disord, 2010 ; 20 (2) : 128-130
Rigid spine syndrome revealing late-onset Pompe disease Neuromuscul Disord, 2010 ; 20 (2) : 128-130
Schmidt, M., Demoule, A., Cracco, C., Gharbi, A., Fiamma, M. N., Straus, C., Duguet, A., Gottfried, S. B., Similowski, T. :
Neurally adjusted ventilatory assist increases respiratory variability and complexity in acute respiratory failure Anesthesiology, 2010 ; 112 (3) : 670-81
Neurally adjusted ventilatory assist increases respiratory variability and complexity in acute respiratory failure Anesthesiology, 2010 ; 112 (3) : 670-81
Drouet, T., Behin, A., Psimaras, D., Choquet, S., Guillevin, R., Hoang Xuan, K. :
Syndrome de Bing-Neel révélateur d’une maladie de Waldenstrom : étude d’un cas et revue de la littérature. Rev Neurol (Paris), 2010 ; 166 (1) : 66-75
Syndrome de Bing-Neel révélateur d’une maladie de Waldenstrom : étude d’un cas et revue de la littérature. Rev Neurol (Paris), 2010 ; 166 (1) : 66-75
