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
Publications (1181)
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
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
Benveniste, O., Hilton-Jones, D. :
International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009 Neuromuscul Disord, 2010 ; 20 (6) : 414-421
International Workshop on Inclusion Body Myositis held at the Institute of Myology, Paris, on 29 May 2009 Neuromuscul Disord, 2010 ; 20 (6) : 414-421
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
