Attarian, S., Salort-Campana, E., Nguyen, K., Behin, A., Urtizberea, J. A. :
Recommendations for the management of facioscapulohumeral muscular dystrophy in 2011
Rev Neurol (Paris), 2012 ; 168 (12) : 910-918
Publications (1184)
Dimitri, D., Eymard, B. :
Myopathies inflammatoires, myopathies necrosantes auto-immunes, myopathies genetiques de l’adulte: frontieres diagnostiques. Rev Med Interne, 2012 ; 33 (3) : 134-142
Myopathies inflammatoires, myopathies necrosantes auto-immunes, myopathies genetiques de l’adulte: frontieres diagnostiques. Rev Med Interne, 2012 ; 33 (3) : 134-142
Jallouli, M., Saadoun, D., Eymard, B., Leroux, G., Haroche, J., Le Thi Huong, D., De Gennes, C., Chapelon, C., Benveniste, O., Wechsler, B., Cacoub, P., Amoura, Z., Piette, J. C., Costedoat-Chalumeau, N. :
The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literature J Neurol, 2012 ; 259 (7) : 1290-7
The association of systemic lupus erythematosus and myasthenia gravis: a series of 17 cases, with a special focus on hydroxychloroquine use and a review of the literature J Neurol, 2012 ; 259 (7) : 1290-7
Prigent, H., Orlikowski, D., Laforet, P., Letilly, N., Falaize, L., Pellegrini, N., Annane, D., Raphael, J. C., Lofaso, F. :
Supine volume drop and diaphragmatic function in adults with Pompe disease Eur Respir J, 2012 ; 39 (6) : 1545-6
Supine volume drop and diaphragmatic function in adults with Pompe disease Eur Respir J, 2012 ; 39 (6) : 1545-6
Yokota, T, Duddy, W, Kolski, H :
Exon Skipping for Nonsense Mutations in Duchenne Muscular Dystrophy: Too Many Mutations, Too Few Patients ? Expert Opin Biol Ther, 2012 ; 12 (9) : 1141-1152
Exon Skipping for Nonsense Mutations in Duchenne Muscular Dystrophy: Too Many Mutations, Too Few Patients ? Expert Opin Biol Ther, 2012 ; 12 (9) : 1141-1152
Cifuentes-Diaz, C., Dubourg, O., Irinopoulou, T., Vigny, M., Lachkar, S., Decker, L., Charnay, P., Denisenko, N., Maisonobe, T., Leger, J. M., Viala, K., Hauw, J. J., Girault, J. A. :
Nodes of ranvier and paranodes in chronic acquired neuropathies PLoS ONE, 2011 ; 6 (1) : e14533
Nodes of ranvier and paranodes in chronic acquired neuropathies PLoS ONE, 2011 ; 6 (1) : e14533
Laloui, K., Wary, C., Carlier, R. Y., Hogrel, J. Y., Caillaud, C., Laforet, P. :
Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat ? Neurology, 2011 ; 77 (6) : 594-5
Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat ? Neurology, 2011 ; 77 (6) : 594-5
Schlossarek, S., Carrier, L. :
The ubiquitin-proteasome system in cardiomyopathies Curr Opin Cardiol, 2011 ; 26 (3) : 190-195
The ubiquitin-proteasome system in cardiomyopathies Curr Opin Cardiol, 2011 ; 26 (3) : 190-195
Barthélémy, I, Barrey, E, Aguilar, P, Uriarte, A, Le Chevoir, M, Thibaud, J L, Voit, T, Blot, S, Hogrel, J Y :
Longitudinal Ambulatory Measurements of Gait Abnormality in Dystrophin-Deficient Dogs BMC Musculoskelet Dis, 2011 ; 12 : 75
Longitudinal Ambulatory Measurements of Gait Abnormality in Dystrophin-Deficient Dogs BMC Musculoskelet Dis, 2011 ; 12 : 75
Francois, V., Klein, A. F., Beley, C., Jollet, A., Lemercier, C., Garcia, L., Furling, D. :
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs Nat Struct Mol Biol, 2011 ; 18 (1) : 85-87
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs Nat Struct Mol Biol, 2011 ; 18 (1) : 85-87
