Publications (1181)

Anthony, K., Arechavala-Gomeza, V., Taylor, L. E., Vulin, A., Kaminoh, Y., Torelli, S., Feng, L., Janghra, N., Bonne, G., Beuvin, M., Barresi, R., Henderson, M., Laval, S., Lourbakos, A., Campion, G., Straub, V., Voit, T., Sewry, C. A., Morgan, J. E., Flanigan, K. M., Muntoni, F. :
Dystrophin quantification: Biological and translational research implications Neurology, 2014 ; 83 (22) : 2062-9
Castiglioni, C., Cassandrini, D., Fattori, F., Bellacchio, E., D'Amico, A., Alvarez, K., Gejman, R., Diaz, J., Santorelli, F. M., Romero, N. B., Bertini, E., Bevilacqua, J. A. :
Muscle MRI and histopathology in ACTA1-related congenital nemaline myopathy Muscle Nerve, 2014 ; 50 (6) : 1011-6
Gauthier, M., Marteyn, A., Denis, J. A., Cailleret, M., Giraud-Triboult, K., Aubert, S., Lecuyer, C., Marie, J., Furling, D., Vernet, R., Yanguas, C., Baldeschi, C., Pietu, G., Peschanski, M., Martinat, C. :
A defective Krab-domain zinc-finger transcription factor contributes to altered myogenesis in myotonic dystrophy type 1 Hum Mol Genet, 2014 ; 22 (25) : 5188-98
PĂ©riĂ©, S, Trollet, C, Mouly, V, Vanneaux, V, Mamchaoui, K, Bouazza, B, Marolleau, J P, LaforĂȘt, P, Chapon, F, Eymard, B, Butler-Browne, G, Larghero, J, Lacau St Guily, J. :
Autologous myoblast transplantation for oculopharyngeal muscular dystrophy: a Phase I/IIa clinical study. Mol Ther, 2014 ; 22 (1) : 219-25
Willis, T. A., Hollingsworth, K. G., Coombs, A., Sveen, M. L., Andersen, S., Stojkovic, T., Eagle, M., Mayhew, A., de Sousa, P. L., Dewar, L., Morrow, J. M., Sinclair, C. D., Thornton, J. S., Bushby, K., Lochmuller, H., Hanna, M. G., Hogrel, J. Y., Carlier, P. G., Vissing, J., Straub, V. :
Quantitative Magnetic Resonance Imaging in Limb-Girdle Muscular Dystrophy 2I: A Multinational Cross-Sectional Study PLoS ONE, 2014 ; 9 (2) : e90377
Ben-Ami, E., Miller, A., Berrih-Aknin, S. :
T cells from autoimmune patients display reduced sensitivity to immunoregulation by mesenchymal stem cells: Role of IL-2 Autoimmun Rev, 2014 ; 13 (2) : 187-96
Degos, B., Laforet, P., Jardel, C., Sedel, F., Jossay-Winter, M., Romero, N. B., Lyon-Caen, O., Tourbah, A. :
POLG mutations associated with remitting/relapsing neurological events J Clin Neurosci, 2014 ; 21 (1) : 186-8
Langhans, C., Weber-Carstens, S., Schmidt, F., Hamati, J., Kny, M., Zhu, X., Wollersheim, T., Koch, S., Krebs, M., Schulz, H., Lodka, D., Saar, K., Labeit, S., Spies, C., Hubner, N., Spranger, J., Spuler, S., Boschmann, M., Dittmar, G., Butler-Browne, G., Mouly, V., Fielitz, J. :
Inflammation-induced acute phase response in skeletal muscle and critical illness myopathy PLoS ONE, 2014 ; 9 (3) : e92048
Sacconi, S., Wahbi, K., Theodore, G., Garcia, J., Salviati, L., Bouhour, F., Vial, C., Duboc, D., Laforet, P., Desnuelle, C. :
Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease Neuromuscul Disord, 2014 ; 24 (7) : 648-650
Bohm, J., Biancalana, V., Malfatti, E., Dondaine, N., Koch, C., Vasli, N., Kress, W., Strittmatter, M., Taratuto, A. L., Gonorazky, H., Laforet, P., Maisonobe, T., Olive, M., Gonzalez-Mera, L., Fardeau, M., Carriere, N., Clavelou, P., Eymard, B., Bitoun, M., Rendu, J., Faure, J., Weis, J., Mandel, J. L., Romero, N. B., Laporte, J. :
Adult-onset autosomal dominant centronuclear myopathy due to BIN1 mutations Brain, 2014 ; 137 (Pt 12) : 3160-70