Yokota, T, Duddy, W, Kolski, H :
Exon Skipping for Nonsense Mutations in Duchenne Muscular Dystrophy: Too Many Mutations, Too Few Patients ?
Expert Opin Biol Ther, 2012 ; 12 (9) : 1141-1152
Publications (1184)
Bencze, M., Negroni, E., Vallese, D., Yacoub-Youssef, H., Chaouch, S., Wolff, A., Aamiri, A., Di Santo, J. P., Chazaud, B., Butler-Browne, G., Savino, W., Mouly, V., Riederer, I. :
Proinflammatory Macrophages Enhance the Regenerative Capacity of Human Myoblasts by Modifying Their Kinetics of Proliferation and Differentiation Mol Ther, 2012 ; 20 (11) : 2168-2179
Proinflammatory Macrophages Enhance the Regenerative Capacity of Human Myoblasts by Modifying Their Kinetics of Proliferation and Differentiation Mol Ther, 2012 ; 20 (11) : 2168-2179
Friedrich, F. W., Wilding, B. R., Reischmann, S., Crocini, C., Lang, P., Charron, P., Muller, O. J., McGrath, M. J., Vollert, I., Hansen, A., Linke, W. A., Hengstenberg, C., Bonne, G., Morner, S., Wichter, T., Madeira, H., Arbustini, E., Eschenhagen, T., Mitchell, C. A., Isnard, R., Carrier, L. :
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy Hum Mol Genet, 2012 ; 21 (14) : 3237-3254
Evidence for FHL1 as a novel disease gene for isolated hypertrophic cardiomyopathy Hum Mol Genet, 2012 ; 21 (14) : 3237-3254
Lillis, S., Abbs, S., Ferreiro, A., Muntoni, F., Jungbluth, H. :
Clinical utility gene card for: Multi-minicore disease Eur J Hum Genet, 2012 ; 20 (2) :
Clinical utility gene card for: Multi-minicore disease Eur J Hum Genet, 2012 ; 20 (2) :
Stanciu, R., Guiguet, M., Musset, L., Touitou, D., Beigelman, C., Rigolet, A., Costedoat-Chalumeau, N., Allenbach, Y., Hervier, B., Dubourg, O., Maisonobe, T., Charuel, J. L., Behin, A., Herson, S., Amoura, Z., Grenier, P., Benveniste, O. :
Antisynthetase Syndrome with Anti-Jo1 Antibodies in 48 Patients: Pulmonary Involvement Predicts Disease-modifying Antirheumatic Drug Use J Rheumatol, 2012 ; 39 (9) : 1835-9
Antisynthetase Syndrome with Anti-Jo1 Antibodies in 48 Patients: Pulmonary Involvement Predicts Disease-modifying Antirheumatic Drug Use J Rheumatol, 2012 ; 39 (9) : 1835-9
Barthélémy, I, Barrey, E, Aguilar, P, Uriarte, A, Le Chevoir, M, Thibaud, J L, Voit, T, Blot, S, Hogrel, J Y :
Longitudinal Ambulatory Measurements of Gait Abnormality in Dystrophin-Deficient Dogs BMC Musculoskelet Dis, 2011 ; 12 : 75
Longitudinal Ambulatory Measurements of Gait Abnormality in Dystrophin-Deficient Dogs BMC Musculoskelet Dis, 2011 ; 12 : 75
Francois, V., Klein, A. F., Beley, C., Jollet, A., Lemercier, C., Garcia, L., Furling, D. :
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs Nat Struct Mol Biol, 2011 ; 18 (1) : 85-87
Selective silencing of mutated mRNAs in DM1 by using modified hU7-snRNAs Nat Struct Mol Biol, 2011 ; 18 (1) : 85-87
McCrone, P., Payan, C. A., Knapp, M., Ludolph, A., Agid, Y., Leigh, P. N., Bensimon, G. :
The Economic Costs of Progressive Supranuclear Palsy and Multiple System Atrophy in France, Germany and the United Kingdom PLoS ONE, 2011 ; 6 (9) : e24369
The Economic Costs of Progressive Supranuclear Palsy and Multiple System Atrophy in France, Germany and the United Kingdom PLoS ONE, 2011 ; 6 (9) : e24369
Vilquin, J. T., Catelain, C., Vauchez, K. :
Cell therapy for muscular dystrophies: advances and challenges Curr Opin Organ Transplant, 2011 ; 16 (6) : 640-649
Cell therapy for muscular dystrophies: advances and challenges Curr Opin Organ Transplant, 2011 ; 16 (6) : 640-649
Bevilacqua, J. A., Monnier, N., Bitoun, M., Eymard, B., Ferreiro, A., Monges, S., Lubieniecki, F., Taratuto, A. L., Laquerriere, A., Claeys, K. G., Marty, I., Fardeau, M., Guicheney, P., Lunardi, J., Romero, N. B. :
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalisation and large areas of myofibrillar disorganisation Neuropathol Appl Neurobiol, 2011 ; 37 (3) : 271-284
Recessive RYR1 mutations cause unusual congenital myopathy with prominent nuclear internalisation and large areas of myofibrillar disorganisation Neuropathol Appl Neurobiol, 2011 ; 37 (3) : 271-284
