Publications (1184)

Hervier, B., Uzunhan, Y., Hachulla, E., Benveniste, O., Nunes, H., Delaval, P., Musset, L., Dubucquoi, S., Wallaert, B., Hamidou, M. :
Antisynthetase syndrome positive for anti-threonyl-tRNA synthetase (anti-PL7) antibodies Eur Respir J, 2011 ; 37 (3) : 714-717
Negroni, E., Vallese, D., Vilquin, J. T., Butler-Browne, G., Mouly, V., Trollet, C. :
Current advances in cell therapy strategies for muscular dystrophies Expert Opin Biol Ther, 2011 ; 11 (2) : 157-176
Cifuentes-Diaz, C., Dubourg, O., Irinopoulou, T., Vigny, M., Lachkar, S., Decker, L., Charnay, P., Denisenko, N., Maisonobe, T., Leger, J. M., Viala, K., Hauw, J. J., Girault, J. A. :
Nodes of ranvier and paranodes in chronic acquired neuropathies PLoS ONE, 2011 ; 6 (1) : e14533
Laloui, K., Wary, C., Carlier, R. Y., Hogrel, J. Y., Caillaud, C., Laforet, P. :
Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat ? Neurology, 2011 ; 77 (6) : 594-5
Schlossarek, S., Carrier, L. :
The ubiquitin-proteasome system in cardiomyopathies Curr Opin Cardiol, 2011 ; 26 (3) : 190-195
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
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
Vilquin, J. T., Catelain, C., Vauchez, K. :
Cell therapy for muscular dystrophies: advances and challenges Curr Opin Organ Transplant, 2011 ; 16 (6) : 640-649
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
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