Stojkovic, T., Behin, A. :
Myasthenies oculaires : diagnostic et traitement.
Rev Neurol (Paris), 2010 ; 166 (12) : 987-997
Publications (1184)
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
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
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
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) :
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
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
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
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
Cirak, S., von Deimling, F., Sachdev, S., Errington, W. J., Herrmann, R., Bonnemann, C., Brockmann, K., Hinderlich, S., Lindner, T. H., Steinbrecher, A., Hoffmann, K., Prive, G. G., Hannink, M., Nurnberg, P., Voit, T. :
Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy Brain, 2010 ; 133 (Pt 7) : 2123-2135
Kelch-like homologue 9 mutation is associated with an early onset autosomal dominant distal myopathy Brain, 2010 ; 133 (Pt 7) : 2123-2135
Lagha, M., Sato, T., Regnault, B., Cumano, A. D., Zuniga, A., Licht, J., Relaix, F., Buckingham, M. :
Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo BMC Genomics, 2010 ; 11 (1) : 696
Transcriptome analyses based on genetic screens for Pax3 myogenic targets in the mouse embryo BMC Genomics, 2010 ; 11 (1) : 696
