Hogrel, J. Y. :
Quantitative myotonia assessment using force relaxation curve modelling
Physiol Meas, 2009 ; 30 (7) : 719-27
Publications (1181)
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
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
Severe and rapidly evolving peripheral neuropathy revealing sporadic Creutzfeldt-Jakob disease J Neurol, 2009 ; 256 (1) : 134-6
Arbogast, S, Beuvin, M, Fraysse, B, Zhou, H, Muntoni, F, Ferreiro, A :
Oxidative stress in SEPN1-related myopathy: from pathophysiology to treatment. Ann Neurol, 2009 ; 65 (6) : 677-686
Oxidative stress in SEPN1-related myopathy: from pathophysiology to treatment. Ann Neurol, 2009 ; 65 (6) : 677-686
Douniol, M., Jacquette, A., Guile, J. M., Tanguy, M. L., Angeard, N., Heron, D., Plaza, M., Cohen, D. :
Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy Eur Child Adolesc Psychiatry, 2009 ; 18 (12) : 705-715
Psychiatric and cognitive phenotype in children and adolescents with myotonic dystrophy Eur Child Adolesc Psychiatry, 2009 ; 18 (12) : 705-715
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
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
Core-rod myopathy caused by mutations in the nebulin gene Neurology, 2009 ; 73 (14) : 1159-61
Bonnefont, J. P., Bastin, J., Behin, A., Djouadi, F. :
Bezafibrate for an inborn mitochondrial beta-oxidation defect N Engl J Med, 2009 ; 360 (8) : 838-40
Bezafibrate for an inborn mitochondrial beta-oxidation defect N Engl J Med, 2009 ; 360 (8) : 838-40
Fromes, Y. :
Anticoagulation et circulation extracorporelle : comment mieux adapter l’hĂ©parinothĂ©rapie ? IRBM, 2009 ; 30 (Supplement 1) : S3-S5
Anticoagulation et circulation extracorporelle : comment mieux adapter l’hĂ©parinothĂ©rapie ? IRBM, 2009 ; 30 (Supplement 1) : S3-S5
Mejat, A., Decostre, V., Li, J., Renou, L., Kesari, A., Hantai, D., Stewart, C. L., Xiao, X., Hoffman, E., Bonne, G., Misteli, T. :
Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy J Cell Biol, 2009 ; 184 (1) : 31-44
Lamin A/C-mediated neuromuscular junction defects in Emery-Dreifuss muscular dystrophy J Cell Biol, 2009 ; 184 (1) : 31-44
