Publications (1181)

Chambon, C., Duteil, D., Vignaud, A., Ferry, A., Messaddeq, N., Malivindi, R., Kato, S., Chambon, P., Metzger, D. :
Myocytic androgen receptor controls the strength but not the mass of limb muscles Proc Natl Acad Sci U S A, 2010 ; 107 (32) : 14327-14332
Laforet, P., Vianey-Saban, C., Vissing, J. :
162nd ENMC International Workshop: Disorders of muscle lipid metabolism in adults 28-30 November 2008, Bussum, The Netherlands Neuromuscul Disord, 2010 ; 20 (4) : 283-9
Stojkovic, T., Behin, A. :
Myasthenies oculaires : diagnostic et traitement. Rev Neurol (Paris), 2010 ; 166 (12) : 987-997
Allamand, V., Merlini, L., Bushby, K. :
166th ENMC International Workshop on Collagen type VI-related Myopathies, 22-24 May 2009, Naarden, The Netherlands Neuromuscul Disord, 2010 ; 20 (5) : 346-354
Durieux, A. C., Prudhon, B., Guicheney, P., Bitoun, M. :
Dynamin 2 and human diseases J Mol Med, 2010 ; 88 (4) : 339-350
McClelland, V., Cullup, T., Bodi, I., Ruddy, D., Buj-Bello, A., Biancalana, V., Boehm, J., Bitoun, M., Miller, O., Jan, W., Menson, E., Amaya, L., Trounce, J., Laporte, J., Mohammed, S., Sewry, C., Raiman, J., Jungbluth, H. :
Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy Am J Med Genet A, 2010 ; 152A (3) : 741-747
Vignaud, A., Hourde, C., Medja, F., Agbulut, O., Butler-Browne, G., Ferry, A. :
Impaired skeletal muscle repair after ischemia-reperfusion injury in mice J Biomed Biotechnol, 2010 ; (724914) :
Blondet, B., Carpentier, G., Ferry, A., Chatonnet, A., Courty, J. :
Localization of butyrylcholinesterase at the neuromuscular junction of normal and acetylcholinesterase knockout mice J Histochem Cytochem, 2010 ; 58 (12) : 1075-82
Gilardeau, C :
Maladie de Charcot-Marie-Tooth (1er volet). Tableau clinique Kiné Actualités, 2010 ; 1207 : 19-23
Parri, V., Katzaki, E., Uliana, V., Scionti, F., Tita, R., Artuso, R., Longo, I., Boschloo, R., Vijzelaar, R., Selicorni, A., Brancati, F., Dallapiccola, B., Zelante, L., Hamel, C. P., Sarda, P., Lalani, S. R., Grasso, R., Buoni, S., Hayek, J., Servais, L., de Vries, B. B., Georgoudi, N., Nakou, S., Petersen, M. B., Mari, F., Renieri, A., Ariani, F. :
High frequency of COH1 intragenic deletions and duplications detected by MLPA in patients with Cohen syndrome Eur J Hum Genet, 2010 ; 18 (10) : 1133-1140