Publications (1181)

Larue, S., Maisonobe, T., Benveniste, O., Chapelon-Abric, C., Lidove, O., Papo, T., Eymard, B., Dubourg, O. :
Distal muscle involvement in granulomatous myositis can mimic inclusion body myositis J Neurol Neurosurg Psychiatry, 2011 ; 82 (6) : 674-7
Senderek, J., Muller, J. S., Dusl, M., Strom, T. M., Guergueltcheva, V., Diepolder, I., Laval, S. H., Maxwell, S., Cossins, J., Krause, S., Muelas, N., Vilchez, J. J., Colomer, J., Mallebrera, C. J., Nascimento, A., Nafissi, S., Kariminejad, A., Nilipour, Y., Bozorgmehr, B., Najmabadi, H., Rodolico, C., Sieb, J. P., Steinlein, O. K., Schlotter, B., Schoser, B., Kirschner, J., Herrmann, R., Voit, T., Oldfors, A., Lindbergh, C., Urtizberea, A., von der Hagen, M., Hubner, A., Palace, J., Bushby, K., Straub, V., Beeson, D., Abicht, A., Lochmuller, H. :
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect Am J Hum Genet, 2011 ; 88 (2) : 162-172
Brinas, L., Richard, P., Quijano-Roy, S., Gartioux, C., Ledeuil, C., Lacene, E., Makri, S., Ferreiro, A., Maugenre, S., Topaloglu, H., Haliloglu, G., Penisson-Besnier, I., Jeannet, P. Y., Merlini, L., Navarro, C., Toutain, A., Chaigne, D., Desguerre, I., de Die-Smulders, C., Dunand, M., Echenne, B., Eymard, B., Kuntzer, T., Maincent, K., Mayer, M., Plessis, G., Rivier, F., Roelens, F., Stojkovic, T., Lia Taratuto, A., Lubieniecki, F., Monges, S., Tranchant, C., Viollet, L., Romero, N. B., Estournet, B., Guicheney, P., Allamand, V. :
Early onset collagen VI myopathies: Genetic and clinical correlations Ann Neurol, 2010 ; 68 (4) : 511-520
Izmiryan, A., Peltekian, E., Paulin, D., Li, Z., Xue, Z. :
Synemin Isoforms in Astroglial and Neuronal Cells from Human Central Nervous System Neurochem Res, 2010 ; 35 (6) : 881-887
Randles, K. N., Lam, L. T., Sewry, C. A., Puckelwartz, M., Furling, D., Wehnert, M., McNally, E. M., Morris, G. E. :
Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle development Dev Dyn, 2010 ; 239 (3) : 998-1009
Scelles, R, Aubert-Godard, A, Gargiulo, M, Avant, M, Gortais, J :
Revealing a child’s pathology : physicians’ experiences Early Child Development and Care, 2010 ; 180 (6) : 743-752
Dargelos, E., Brule, C., Stuelsatz, P., Mouly, V., Veschambre, P., Cottin, P., Poussard, S. :
Up-regulation of calcium-dependent proteolysis in human myoblasts under acute oxidative stress Exp Cell Res, 2010 ; 316 (1) : 115-125
Levy, N., Wein, N., Barthelemy, F., Mouly, V., Garcia, L., Krahn, M., Bartoli, M. :
Therapeutic exon ‘switching’ for dysferlinopathies? Eur J Hum Genet, 2010 ; 18 (9) : 969-970
Vaillend, C., Perronnet, C., Ros, C., Gruszczynski, C., Goyenvalle, A., Laroche, S., Danos, O., Garcia, L., Peltekian, E. :
Rescue of a Dystrophin-like Protein by Exon Skipping In Vivo Restores GABA(A)-receptor Clustering in the Hippocampus of the mdx Mouse Mol Ther, 2010 ; 18 (9) : 1683-1688
Baligand, C., Gilson, H., Menard, J. C., Schakman, O., Wary, C., Thissen, J. P., Carlier, P. G. :
Functional assessment of skeletal muscle in intact mice lacking myostatin by concurrent NMR imaging and spectroscopy Gene Ther, 2010 ; 17 (3) : 328-37