Allamand, V, Brinas, L, Richard , P, Stojkovic, T, Quijano-Roy, S, Bonne, G :
ColVI-myopathies: where do we stand, where do we go ?
Skelet Muscle, 2011 ; 1 (1) : 30
Publications (1181)
Dubourg, O., Wanschitz, J., Maisonobe, T., Behin, A., Allenbach, Y., Herson, S., Benveniste, O. :
Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis Acta Myol, 2011 ; 30 (2) : 103-8
Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis Acta Myol, 2011 ; 30 (2) : 103-8
Lokireddy, S., Mouly, V., Butler-Browne, G., Gluckman, P. D., Sharma, M., Kambadur, R., McFarlane, C. :
Myostatin promotes the wasting of human myoblast cultures through promoting ubiquitin-proteasome pathway-mediated loss of sarcomeric proteins Am J Physiol Cell Physiol, 2011 ; 301 (6) : C1316-1324
Myostatin promotes the wasting of human myoblast cultures through promoting ubiquitin-proteasome pathway-mediated loss of sarcomeric proteins Am J Physiol Cell Physiol, 2011 ; 301 (6) : C1316-1324
Toussaint, A., Cowling, B. S., Hnia, K., Mohr, M., Oldfors, A., Schwab, Y., Yis, U., Maisonobe, T., Stojkovic, T., Wallgren-Pettersson, C., Laugel, V., Echaniz-Laguna, A., Mandel, J. L., Nishino, I., Laporte, J. :
Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies Acta Neuropathol, 2011 ; 121 (2) : 253-266
Defects in amphiphysin 2 (BIN1) and triads in several forms of centronuclear myopathies Acta Neuropathol, 2011 ; 121 (2) : 253-266
Benveniste, O., Leger, J. M. :
Inflammatory or necrotizing myopathies, myositides and other acquired myopathies, new insight in 2011 Presse Med, 2011 ; 40 (4 Pt 2) : e197-8
Inflammatory or necrotizing myopathies, myositides and other acquired myopathies, new insight in 2011 Presse Med, 2011 ; 40 (4 Pt 2) : e197-8
Hanisch, F., Muller, T., Dietz, A., Bitoun, M., Kress, W., Weis, J., Stoltenburg, G., Zierz, S. :
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations J Neurol, 2011 ; 258 (6) : 1085-90
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations J Neurol, 2011 ; 258 (6) : 1085-90
Meune, C., Wahbi, K., Weber, S., Zuily, S., Cynober, L., Chenevier-Gobeaux, C. :
Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome Clin Biochem, 2011 ; 44 (16) : 1343-1345
Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome Clin Biochem, 2011 ; 44 (16) : 1343-1345
Castets, P., Bertrand, A. T., Beuvin, M., Ferry, A., Le Grand, F., Castets, M., Chazot, G., Rederstorff, M., Krol, A., Lescure, A., Romero, N. B., Guicheney, P., Allamand, V. :
Satellite cell loss and impaired muscle regeneration in Selenoprotein N deficiency Hum Mol Genet, 2011 ; 20 (4) : 694-704
Satellite cell loss and impaired muscle regeneration in Selenoprotein N deficiency Hum Mol Genet, 2011 ; 20 (4) : 694-704
Klein, A. F., Gasnier, E., Furling, D. :
Gain of RNA function in pathological cases: Focus on myotonic dystrophy Biochimie, 2011 ; 93 (11) : 2006-12
Gain of RNA function in pathological cases: Focus on myotonic dystrophy Biochimie, 2011 ; 93 (11) : 2006-12
Redondo-Verge, L., Benyaou, R., Fernandez-Recio, M., Dinca, L., Richard, P., Bonne, G. :
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophy Muscle Nerve, 2011 ; 44 (4) : 587-9
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophy Muscle Nerve, 2011 ; 44 (4) : 587-9
