Publications (1184)

Seferian, A. M., Moraux, A., Canal, A., Decostre, V., Diebate, O., Le Moing, A. G., Gidaro, T., Deconinck, N., Van Parys, F., Vereecke, W., Wittevrongel, S., Annoussamy, M., Mayer, M., Maincent, K., Cuisset, J. M., Tiffreau, V., Denis, S., Jousten, V., Quijano-Roy, S., Voit, T., Hogrel, J. Y., Servais, L. :
Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial PLoS ONE, 2015 ; 10 (4) : e0121799
Azzabou, N., Hogrel, J. Y., Carlier, P. G. :
NMR based biomarkers to study age-related changes in the human quadriceps Exp Gerontol, 2015 ; 70 : 54-60
Mariot, V, Roche, S, Hourdé, C, Portilho, D, Sacconi, S, Puppo, P, Duguez, S, Rameau, P, Caruso, N, Delezoide, A L, Desnuelle, C, Bessières, B, Collardeau, S, Feasson, L, Maisonobe, T, Magdinier, F, Helmbacher, F, Butler-Browne, G, Mouly, V, Dumonceaux, J :
Correlation between low FAT1 expression and early affected muscle in facioscapulohumeral muscular dystrophy. Ann Neurol, 2015 ; 78 (3) : 387-400
Todd, E. J., Yau, K. S., Ong, R., Slee, J., McGillivray, G., Barnett, C. P., Haliloglu, G., Talim, B., Akcoren, Z., Kariminejad, A., Cairns, A., Clarke, N. F., Freckmann, M. L., Romero, N. B., Williams, D., Sewry, C. A., Colley, A., Ryan, M. M., Kiraly-Borri, C., Sivadorai, P., Allcock, R. J., Beeson, D., Maxwell, S., Davis, M. R., Laing, N. G., Ravenscroft, G. :
Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth Orphanet J Rare Dis, 2015 ; 10 (1) : 148
Junge, N., Mingozzi, F., Ott, M., Baumann, U. :
Adeno-associated Virus Vector Based Gene Therapy for Monogenetic Metabolic Diseases of the Liver J Pediatr Gastroenterol Nutr, 2015 ; 60 (4) : 433-440
Zocevic, A., Rouillon, J., Wong, B., Servais, L., Voit, T., Svinartchouk, F. :
Evaluation of the serum matrix metalloproteinase-9 as a biomarker for monitoring disease progression in Duchenne muscular dystrophy Neuromuscul Disord, 2015 ; 25 (5) : 444-446
Carpentier, M., Lorain, S., Chappert, P., Lalfer, M., Hardet, R., Urbain, D., Peccate, C., Adriouch, S., Garcia, L., Davoust, J., Gross, D. A. :
Intrinsic transgene immunogenicity gears CD8(+) T-cell priming after rAAV-mediated muscle gene transfer Mol Ther, 2015 ; 23 (4) : 697-706
Gomez-Andres, D., Dabaj, I., Mompoint, D., Hankiewicz, K., Azzi, V., Ioos, C., Romero, N. B., Ben Yaou, R., Bergounioux, J., Bonne, G., Richard, P., Estournet, B., Yves-Carlier, R., Quijano-Roy, S. :
Pediatric laminopathies: Whole-body MRI fingerprint and comparison with SEPN1-myopathy Muscle Nerve, 2015 ; :
Svahn, J., Streichenberger, N., Benveniste, O., Menassa, R., Michel, L., Fayolle, H., Petiot, P. :
Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations Neuromuscul Disord, 2015 ; 25 (11) : 865-8
Decorte, N., Lamalle, L., Carlier, P. G., Giacomini, E., Guinot, M., Levy, P., Verges, S., Wuyam, B. :
Impact of salbutamol on muscle metabolism assessed by PNMR spectroscopy Scand J Med Sci Sports, 2015 ; 25 (3) : e267-73