Vulin, A., Barthelemy, I., Goyenvalle, A., Thibaud, J. L., Beley, C., Griffith, G., Benchaouir, R., le Hir, M., Unterfinger, Y., Lorain, S., Dreyfus, P., Voit, T., Carlier, P. G., Blot, S., Garcia, L. :
Muscle Function Recovery in Golden Retriever Muscular Dystrophy After AAV1-U7 Exon Skipping
Mol Ther, 2012 ; 20 (11) : 2120-33
Publications (1181)
Durr, A., Gargiulo, M., Feingold, J. :
La phase présymptomatique de la maladie de Huntington , 2012 ; 168 (11) : 806-808
La phase présymptomatique de la maladie de Huntington , 2012 ; 168 (11) : 806-808
Amthor, H., Hoogaars, W. M. :
Interference with Myostatin/ActRIIB Signaling as a Therapeutic Strategy for Duchenne Muscular Dystrophy Curr Gene Ther, 2012 ; 12 (3) : 245-259
Interference with Myostatin/ActRIIB Signaling as a Therapeutic Strategy for Duchenne Muscular Dystrophy Curr Gene Ther, 2012 ; 12 (3) : 245-259
Didier, N., Hourde, C., Amthor, H., Marazzi, G., Sassoon, D. :
Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle EMBO Mol Med, 2012 ; 4 (9) : 910-23
Loss of a single allele for Ku80 leads to progenitor dysfunction and accelerated aging in skeletal muscle EMBO Mol Med, 2012 ; 4 (9) : 910-23
Huguet, A, Medja, F, Nicole, A, Vignaud, A, Guiraud-Dogan, C, Ferry, A, Decostre, V, Hogrel, J Y, Metzger, F, Hoeflich, A, Baraibar, M, Gomes-Pereira, M, Puymirat, J, Bassez, G, Furling, D, Munnich, A, Gourdon, G :
Molecular, physiological and motor performance defects in DMSXL mice carrying >1000 CTG repeats from the human DM1 locus PLoS Genet, 2012 ; 8 (11) : e1003043
Molecular, physiological and motor performance defects in DMSXL mice carrying >1000 CTG repeats from the human DM1 locus PLoS Genet, 2012 ; 8 (11) : e1003043
Preisler, N., Orngreen, M. C., Echaniz-Laguna, A., Laforet, P., Lonsdorfer-Wolf, E., Doutreleau, S., Geny, B., Akman, H. O., Dimauro, S., Vissing, J. :
Muscle phosphorylase kinase deficiency: A neutral metabolic variant or a disease? Neurology, 2012 ; 78 (4) : 265-8
Muscle phosphorylase kinase deficiency: A neutral metabolic variant or a disease? Neurology, 2012 ; 78 (4) : 265-8
Yger, M., Stojkovic, T., Tardieu, S., Maisonobe, T., Brice, A., Echaniz-Laguna, A., Alembik, Y., Girard, S., Cazeneuve, C., Leguern, E., Dubourg, O. :
Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C J Peripher Nerv Syst, 2012 ; 17 (1) : 112-122
Characteristics of clinical and electrophysiological pattern of Charcot-Marie-Tooth 4C J Peripher Nerv Syst, 2012 ; 17 (1) : 112-122
Benchaouir, R., Goyenvalle, A. :
Splicing Modulation Mediated by Small Nuclear RNAs as Therapeutic Approaches for Muscular Dystrophies Curr Gene Ther, 2012 ; 12 (3) : 179-191
Splicing Modulation Mediated by Small Nuclear RNAs as Therapeutic Approaches for Muscular Dystrophies Curr Gene Ther, 2012 ; 12 (3) : 179-191
Friedrich, F. W., Carrier, L. :
Genetics of hypertrophic and dilated cardiomyopathy Curr Pharm Biotechnol, 2012 ; 13 (13) : 2467-76
Genetics of hypertrophic and dilated cardiomyopathy Curr Pharm Biotechnol, 2012 ; 13 (13) : 2467-76
Li, K., Hogrel, J. Y., Duchene, J., Hewson, D. J. :
Analysis of fatigue and tremor during sustained maximal grip contractions using Hilbert-Huang Transformation Med Eng Phys, 2012 ; 34 (7) : 832-840
Analysis of fatigue and tremor during sustained maximal grip contractions using Hilbert-Huang Transformation Med Eng Phys, 2012 ; 34 (7) : 832-840
