Lorain, S, Peccate, C, Le Hir, M, Garcia, L :
Exon Exchange Approach to Repair Duchenne Dystrophin Transcripts
PLoS ONE, 2010 ; 5 (5) : e10894
Publications (1184)
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
LaforĂȘt, P :
Cerebral vessel involvement in Pompe disease. The Steps Forward in Pompe Disease -3rd European Symposium, Munich, Germany, November 20 and 21 2009 Clin Ther, 2010 ; 32 (Supplement 2) : S51
Cerebral vessel involvement in Pompe disease. The Steps Forward in Pompe Disease -3rd European Symposium, Munich, Germany, November 20 and 21 2009 Clin Ther, 2010 ; 32 (Supplement 2) : S51
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 rĂ©vĂ©lateur d’une maladie de Waldenstrom : Ă©tude d’un cas et revue de la littĂ©rature. Rev Neurol (Paris), 2010 ; 166 (1) : 66-75
Syndrome de Bing-Neel rĂ©vĂ©lateur d’une maladie de Waldenstrom : Ă©tude d’un cas et revue de la littĂ©rature. Rev Neurol (Paris), 2010 ; 166 (1) : 66-75
