Yaou, R. B., De Sandre-Giovannoli, A., Leturcq, F., Levy, N., Bonne, G. :
Premiere reunion franco-italienne des laminopathies et autres pathologies liees a l’enveloppe nucleaire
Med Sci (Paris), 2015 ; 31 Spec No 3 : 39-40
Publications (1181)
Hamel, Y., Mamoune, A., Mauvais, F. X., Habarou, F., Lallement, L., Romero, N. B., Ottolenghi, C., de Lonlay, P. :
Acute rhabdomyolysis and inflammation J Inherit Metab Dis, 2015 ; 38 (4) : 621-628
Acute rhabdomyolysis and inflammation J Inherit Metab Dis, 2015 ; 38 (4) : 621-628
Tuzun, E., Berrih-Aknin, S., Brenner, T., Kusner, L. L., Le Panse, R., Yang, H., Tzartos, S., Christadoss, P. :
Guidelines for standard preclinical experiments in the mouse model of myasthenia gravis induced by acetylcholine receptor immunization Exp Neurol, 2015 ; 270 : 11-17
Guidelines for standard preclinical experiments in the mouse model of myasthenia gravis induced by acetylcholine receptor immunization Exp Neurol, 2015 ; 270 : 11-17
de la Vaissiere, S., Toutain, A., Chene, M. A., Lagrue, E., Cantagrel, S., Provost, S., Eymard, B., Castelnau, P. :
Syndromes myastheniques congenitaux de l’enfant : strategies therapeutiques medicamenteuses Arch Pediatr, 2015 ; 22 (7) : 724-8
Syndromes myastheniques congenitaux de l’enfant : strategies therapeutiques medicamenteuses Arch Pediatr, 2015 ; 22 (7) : 724-8
Wirth, B., Barkats, M., Martinat, C., Sendtner, M., Gillingwater, T. H. :
Moving towards treatments for spinal muscular atrophy: hopes and limits Expert Opin Emerg Drugs, 2015 ; 20 (3) : 353-6
Moving towards treatments for spinal muscular atrophy: hopes and limits Expert Opin Emerg Drugs, 2015 ; 20 (3) : 353-6
Behin, A., Salort-Campana, E., Wahbi, K., Richard, P., Carlier, R. Y., Carlier, P., Laforet, P., Stojkovic, T., Maisonobe, T., Verschueren, A., Franques, J., Attarian, S., Maues de Paula, A., Figarella-Branger, D., Becane, H. M., Nelson, I., Duboc, D., Bonne, G., Vicart, P., Udd, B., Romero, N., Pouget, J., Eymard, B. :
Myofibrillar myopathies: State of the art, present and future challenges Rev Neurol (Paris), 2015 ; 171 (10) : 715-29
Myofibrillar myopathies: State of the art, present and future challenges Rev Neurol (Paris), 2015 ; 171 (10) : 715-29
Allenbach, Y, Guiguet, M, Rigolet, A, Marie, I, Hachulla, E, Drouot, L, Jouen, F, Jacquot, S, Mariampillai, K, Musset, L, Grenier, P, Devilliers, H, Hij, A, Boyer, O, Herson, S, Benveniste, O :
Efficacy of Rituximab in Refractory Inflammatory Myopathies Associated with Anti- Synthetase Auto-Antibodies: an Open-Label, Phase II Trial PLoS ONE, 2015 ; (SP) :
Efficacy of Rituximab in Refractory Inflammatory Myopathies Associated with Anti- Synthetase Auto-Antibodies: an Open-Label, Phase II Trial PLoS ONE, 2015 ; (SP) :
Maurer, M., Bougoin, S., Feferman, T., Frenkian, M., Bismuth, J., Mouly, V., Clairac, G., Tzartos, S., Fadel, E., Eymard, B., Fuchs, S., Souroujon, M. C., Berrih-Aknin, S. :
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
De Cid, R., Ben Yaou, R., Roudaut, C., Charton, K., Baulande, S., Leturcq, F., Romero, N. B., Malfatti, E., Beuvin, M., Vihola, A., Criqui, A., Nelson, I., Nectoux, J., Ben Aim, L., Caloustian, C., Olaso, R., Udd, B., Bonne, G., Eymard, B., Richard, I. :
A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy Neurology, 2015 ; 85 (24) : 2126-35
A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy Neurology, 2015 ; 85 (24) : 2126-35
Chartier, A., Klein, P., Pierson, S., Barbezier, N., Gidaro, T., Casas, F., Carberry, S., Dowling, P., Maynadier, L., Bellec, M., Oloko, M., Jardel, C., Moritz, B., Dickson, G., Mouly, V., Ohlendieck, K., Butler-Browne, G., Trollet, C., Simonelig, M. :
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
