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
Publications (1181)
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
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
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
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
Maillart, E., Acquaviva-Bourdain, C., Rigal, O., Brivet, M., Jardel, C., Lombes, A., Eymard, B., Vianey-Saban, C., Laforet, P. :
Deficit multiple en acyl-CoA deshydrogenases : une cause traitable de lipidose musculaire d’origine genetique. Rev Neurol (Paris), 2010 ; 166 (3) : 289-94
Deficit multiple en acyl-CoA deshydrogenases : une cause traitable de lipidose musculaire d’origine genetique. Rev Neurol (Paris), 2010 ; 166 (3) : 289-94
Viala, K., Maisonobe, T., Stojkovic, T., Koutlidis, R., Ayrignac, X., Musset, L., Fournier, E., Leger, J. M., Bouche, P. :
A current view of the diagnosis, clinical variants, response to treatment and prognosis of chronic inflammatory demyelinating polyradiculoneuropathy J Peripher Nerv Syst, 2010 ; 15 (1) : 50-6
A current view of the diagnosis, clinical variants, response to treatment and prognosis of chronic inflammatory demyelinating polyradiculoneuropathy J Peripher Nerv Syst, 2010 ; 15 (1) : 50-6
Gaudon, K., Penisson-Besnier, I., Chabrol, B., Bouhour, F., Demay, L., Ben Ammar, A., Bauche, S., Vial, C., Nicolas, G., Eymard, B., Hantai, D., Richard, P. :
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing J Med Genet, 2010 ; 47 (12) : 795-796
Multiexon deletions account for 15% of congenital myasthenic syndromes with RAPSN mutations after negative DNA sequencing J Med Genet, 2010 ; 47 (12) : 795-796
Pannerec, A., Sassoon, D. :
Identification d’une nouvelle population de cellules souches musculaires. Med Sci (Paris), 2010 ; 26 (10) : 797-800
Identification d’une nouvelle population de cellules souches musculaires. Med Sci (Paris), 2010 ; 26 (10) : 797-800
