Publications (1184)

Marmursztejn, J., Vignaux, O., Goffinet, F., Cabanes, L., Duboc, D. :
Delayed-enhanced cardiac magnetic resonance imaging features in peripartum cardiomyopathy Int J Cardiol, 2009 ; 137 (3) : e63-4
Umapathi, T., Hughes, R. A., Nobile-Orazio, E., Leger, J. M. :
Immunosuppressant and immunomodulatory treatments for multifocal motor neuropathy Cochrane Database Syst Rev, 2009 ; CD003217 (1) :
Blanc, F. X., Coirault, C., Oliviero, P., Lecarpentier, Y. :
Relaxation of tracheal smooth muscle is impaired in innate airway hyperresponsiveness Eur Respir J, 2009 ; 34 (2) : 417-24
Frikha, F., Rigolet, A., Behin, A., Fautrel, B., Herson, S., Benveniste, O. :
Efficacy of rituximab in refractory and relapsing myositis with anti-JO1 antibodies: a report of two cases Rheumatology (Oxford), 2009 ; 48 (9) : 1166-1168
Hogrel, J. Y. :
Quantitative myotonia assessment using force relaxation curve modelling Physiol Meas, 2009 ; 30 (7) : 719-27
Nadaj-Pakleza, A. A., Vincitorio, C. M., Laforet, P., Eymard, B., Dion, E., Teijeira, S., Vietez, I., Jeanpierre, M., Navarro, C., Stojkovic, T. :
Permanent muscle weakness in MCArdle disease Muscle Nerve, 2009 ; 40 (3) : 350-7
Zephir, H., Stojkovic, T., de Seze, J., Maurage, C. A., Peoc'h, K., Haik, S., Vermersch, P. :
Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease J Neurol, 2009 ; 256 (1) : 134-6
Clarencon, F., Jafari, A., Lefevre, M., Perie, S., Angelard, B., Marsault, C., Tassart, M. :
Infraorbital nerve schwannoma J Neuroradiol, 2009 ; 36 (5) : 301-303
Lagha, M., Brunelli, S., Messina, G., Cumano, A., Kume, T., Relaix, F., Buckingham, M. E. :
Pax3:Foxc2 reciprocal repression in the somite modulates muscular versus vascular cell fate choice in multipotent progenitors Dev Cell, 2009 ; 17 (6) : 892-9
Romero, N. B., Lehtokari, V. L., Quijano-Roy, S., Monnier, N., Claeys, K. G., Carlier, R. Y., Pellegrini, N., Orlikowski, D., Barois, A., Laing, N. G., Lunardi, J., Fardeau, M., Pelin, K., Wallgren-Pettersson, C. :
Core-rod myopathy caused by mutations in the nebulin gene Neurology, 2009 ; 73 (14) : 1159-61