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
Publications (1181)
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
Susman, R. D., Quijano-Roy, S., Yang, N., Webster, R., Clarke, N. F., Dowling, J., Kennerson, M., Nicholson, G., Biancalana, V., Ilkovski, B., Flanigan, K., Arbuckle, S., Malladi, C., Robinson, P., Vucic, S., Mayer, M., Romero, N. B., Urtizberea, J. A., Garcia-Bragado, F., Guicheney, P., Bitoun, M., Carlier, R. Y., North, K. N. :
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy Neuromuscul Disord, 2010 ; 20 (4) : 229-237
Expanding the clinical, pathological and MRI phenotype of DNM2-related centronuclear myopathy Neuromuscul Disord, 2010 ; 20 (4) : 229-237
Arbogast, S, Ferreiro, A :
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Durieux, A. C., Vignaud, A., Prudhon, B., Viou, M. T., Beuvin, M., Vassilopoulos, S., Fraysse, B., Ferry, A., Laine, J., Romero, N. B., Guicheney, P., Bitoun, M. :
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
Mearini, G., Gedicke, C., Schlossarek, S., Witt, C. C., Kramer, E., Cao, P., Gomes, M. D., Lecker, S. H., Labeit, S., Willis, M. S., Eschenhagen, T., Carrier, L. :
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Vuillerot, C., Girardot, F., Payan, C., Fermanian, J., Iwaz, J., De Lattre, C, Berard, C. :
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
