Aouizerate, J., De Antonio, M., Bassez, G., Gherardi, R. K., Berenbaum, F., Guillevin, L., Berezne, A., Valeyre, D., Maisonobe, T., Dubourg, O., Cosnes, A., Benveniste, O., Authier, F. J. :
Myofiber HLA-DR expression is a distinctive biomarker for antisynthetase-associated myopathy
Acta Neuropathol Commun, 2014 ; 2 : 154
Publications (1181)
Chatzifrangkeskou, M., Bonne, G., Muchir, A. :
Nuclear envelope and striated muscle diseases Curr Opin Cell Biol, 2014 ; 32C : 1-6
Nuclear envelope and striated muscle diseases Curr Opin Cell Biol, 2014 ; 32C : 1-6
Gradolatto, A., Nazzal, D., Truffault, F., Bismuth, J., Fadel, E., Foti, M., Berrih-Aknin, S. :
Both Treg cells and Tconv cells are defective in the Myasthenia gravis thymus: Roles of IL-17 and TNF-alpha J Autoimmun, 2014 ; 52 : 53-63
Both Treg cells and Tconv cells are defective in the Myasthenia gravis thymus: Roles of IL-17 and TNF-alpha J Autoimmun, 2014 ; 52 : 53-63
Possidonio, A. C., Soares, C. P., Portilho, D. M., Midlej, V., Benchimol, M., Butler-Browne, G., Costa, M. L., Mermelstein, C. :
Differences in the expression and distribution of flotillin-2 in chick, mice and human muscle cells PLoS ONE, 2014 ; 9 (8) : e103990
Differences in the expression and distribution of flotillin-2 in chick, mice and human muscle cells PLoS ONE, 2014 ; 9 (8) : e103990
Yuen, M., Sandaradura, S. A., Dowling, J. J., Kostyukova, A. S., Moroz, N., Quinlan, K. G., Lehtokari, V. L., Ravenscroft, G., Todd, E. J., Ceyhan-Birsoy, O., Gokhin, D. S., Maluenda, J., Lek, M., Nolent, F., Pappas, C. T., Novak, S. M., D'Amico, A., Malfatti, E., Thomas, B. P., Gabriel, S. B., Gupta, N., Daly, M. J., Ilkovski, B., Houweling, P. J., Davidson, A. E., Swanson, L. C., Brownstein, C. A., Gupta, V. A., Medne, L., Shannon, P., Martin, N., Bick, D. P., Flisberg, A., Holmberg, E., Van den Bergh, P., Lapunzina, P., Waddell, L. B., Sloboda, D. D., Bertini, E., Chitayat, D., Telfer, W. R., Laquerriere, A., Gregorio, C. C., Ottenheijm, C. A., Bonnemann, C. G., Pelin, K., Beggs, A. H., Hayashi, Y. K., Romero, N. B., Laing, N. G., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V. M., MacArthur, D. G., North, K. N., Clarke, N. F. :
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy J Clin Invest, 2014 ; 124 (11) : 4693-4708
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy J Clin Invest, 2014 ; 124 (11) : 4693-4708
Benveniste, O. :
Le muscle inflammatoire : avancés en 2014 Rev Med Interne, 2014 ; 35 (7) : 411-412
Le muscle inflammatoire : avancés en 2014 Rev Med Interne, 2014 ; 35 (7) : 411-412
Devic, P., Petiot, P., Simonet, T., Stojkovic, T., Delmont, E., Franques, J., Magot, A., Vial, C., Lagrange, E., Nicot, A. S., Risson, V., Eymard, B., Schaeffer, L. :
Antibodies to clustered acetylcholine receptor: expanding the phenotype Eur J Neurol, 2014 ; 21 (1) : 130-4
Antibodies to clustered acetylcholine receptor: expanding the phenotype Eur J Neurol, 2014 ; 21 (1) : 130-4
Le Guiner, C, Montus, M, Servais, L, Cherel, Y, Francois, V, Thibaud, JL, Wary, C, Matot, B, Larcher, T, Guigand, L, Dutilleul, M, Domenger, C, Allais, M, Beuvin, M, Moraux, A, Le Duff, J, Devaux, M, Jaulin, N, Guilbaud, M, Latournerie, V, Veron, P, Boutin, S, Leborgne, C, Desgue, D, Deschamps, JY, Moullec, S, Fromes, Y, Vulin, A, Smith, RH, Laroudie, N, Barnay-Toutain, F, RiviĂšre, C, Bucher, S, Hoa Le, T, Delaunay, N, Gasmi, M, Kotin, RM, Bonne, G, Adjali, O, Masurier, C, Hogrel, J. Y., Carlier, P, Moullier, P, Voit, T :
Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients Mol Ther, 2014 ; 22(11):1923-35 (11) : 1923-35
Forelimb Treatment in a Large Cohort of Dystrophic Dogs Supports Delivery of a Recombinant AAV for Exon Skipping in Duchenne Patients Mol Ther, 2014 ; 22(11):1923-35 (11) : 1923-35
Schreckenbach, T., Schroder, J. M., Voit, T., Abicht, A., Neuen-Jacob, E., Roos, A., Bulst, S., Kuhl, C., Schulz, J. B., Weis, J., Claeys, K. G. :
Novel TPM3 mutation in a family with cap myopathy and review of the literature Neuromuscul Disord, 2014 ; 24 (2) : 117-24
Novel TPM3 mutation in a family with cap myopathy and review of the literature Neuromuscul Disord, 2014 ; 24 (2) : 117-24
Bohm, J., Chevessier, F., Koch, C., Peche, G. A., Mora, M., Morandi, L., Pasanisi, B., Moroni, I., Tasca, G., Fattori, F., Ricci, E., Penisson-Besnier, I., Nadaj-Pakleza, A., Fardeau, M., Joshi, P. R., Deschauer, M., Romero, N. B., Eymard, B., Laporte, J. :
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1 J Med Genet, 2014 ; 51 (12) : 824-33
Clinical, histological and genetic characterisation of patients with tubular aggregate myopathy caused by mutations in STIM1 J Med Genet, 2014 ; 51 (12) : 824-33
