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
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
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
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