McFarlane, C., Gu, Z. H., Wong, Z. W., Lau, H. Y., Lokireddy, S., Ge, X., Mouly, V., Butler-Browne, G., Gluckman, P. D., Sharma, M., Kambadur, R. :
Human myostatin negatively regulates human myoblast growth and differentiation
Am J Physiol Cell Physiol, 2011 ; 301 (1) : C195-203
Publications (1184)
Vrolix, K., Niks, E. H., Le Panse, R., van Ostaijen-Ten Dam, M. M., Muris, A. H., Jol-van der Zijde, C. M., van Tol, M. J., Losen, M., Molenaar, P. C., van Zoelen, E. J., Berrih-Aknin, S., De Baets, M. H., Verschuuren, J. J., Martinez-Martinez, P. :
Reduced thymic expression of ErbB receptors without auto-antibodies against synaptic ErbB in myasthenia gravis J Neuroimmunol, 2011 ; 232 (1-2) : 158-165
Reduced thymic expression of ErbB receptors without auto-antibodies against synaptic ErbB in myasthenia gravis J Neuroimmunol, 2011 ; 232 (1-2) : 158-165
Boccara, F., Mary-Krause, M., Teiger, E., Lang, S., Lim, P., Wahbi, K., Beygui, F., Milleron, O., Gabriel Steg, P., Funck-Brentano, C., Slama, M., Girard, P. M., Costagliola, D., Cohen, A. :
Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosis Eur Heart J, 2011 ; 32 (1) : 41-50
Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosis Eur Heart J, 2011 ; 32 (1) : 41-50
Hogrel, J. Y. :
DM1 et essais thérapeutiques : critères neuromusculaires d’évaluation Cahier de Myologie, 2011 ; 5 : 11-14
DM1 et essais thérapeutiques : critères neuromusculaires d’évaluation Cahier de Myologie, 2011 ; 5 : 11-14
Orlikowski, D., Pellegrini, N., Prigent, H., Laforet, P., Carlier, R., Carlier, P. G., Eymard, B., Lofaso, F., Annane, D. :
Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease Neuromuscul Disord, 2011 ; 21 (7) : 477-482
Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease Neuromuscul Disord, 2011 ; 21 (7) : 477-482
Dallerac, G., Perronnet, C., Chagneau, C., Leblanc-Veyrac, P., Samson-Desvignes, N., Peltekian, E., Danos, O., Garcia, L., Laroche, S., Billard, J. M., Vaillend, C. :
Rescue of a dystrophin-like protein by exon skipping normalizes synaptic plasticity in the hippocampus of the mdx mouse Neurobiol Dis, 2011 ; 43 (3) : 635-641
Rescue of a dystrophin-like protein by exon skipping normalizes synaptic plasticity in the hippocampus of the mdx mouse Neurobiol Dis, 2011 ; 43 (3) : 635-641
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
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
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect Am J Hum Genet, 2011 ; 88 (2) : 162-172
Ben Yaou, R., Navarro, C., Quijano-Roy, S., Bertrand, A. T., Massart, C., De Sandre-Giovannoli, A., Cadinanos, J., Mamchaoui, K., Butler-Browne, G., Estournet, B., Richard, P., Barois, A., Levy, N., Bonne, G. :
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation Eur J Hum Genet, 2011 ; 19 (6) : 647-654
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation Eur J Hum Genet, 2011 ; 19 (6) : 647-654
Fugier, C., Klein, A. F., Hammer, C., Vassilopoulos, S., Ivarsson, Y., Toussaint, A., Tosch, V., Vignaud, A., Ferry, A., Messaddeq, N., Kokunai, Y., Tsuburaya, R., de la Grange, P., Dembele, D., Francois, V., Precigout, G., Boulade-Ladame, C., Hummel, M. C., de Munain, A. L., Sergeant, N., Laquerriere, A., Thibault, C., Deryckere, F., Auboeuf, D., Garcia, L., Zimmermann, P., Udd, B., Schoser, B., Takahashi, M. P., Nishino, I., Bassez, G., Laporte, J., Furling, D., Charlet-Berguerand, N. :
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy Nat Med, 2011 ; 17 (6) : 720-5
Misregulated alternative splicing of BIN1 is associated with T tubule alterations and muscle weakness in myotonic dystrophy Nat Med, 2011 ; 17 (6) : 720-5
