Publications (1181)

Dany, A., Rapin, A., Lavrard, B., Saout, V., Reveillere, C., Bassez, G., Tiffreau, V., Pereon, Y., Sacconi, S., Eymard, B., Drame, M., Jolly, D., Novella, J. L., Hardouin, J. B., Boyer, F. C. :
Quality of Life in Patients with Genetic Neuromuscular Disease Questionnaire: Rasch validation of the French Version (QoL-gNMD) Muscle Nerve, 2017 ; (SP) :
Moulin, M., Ferreiro, A. :
Muscle redox disturbances and oxidative stress as pathomechanisms and therapeutic targets in early-onset myopathies Semin Cell Dev Biol, 2017 ; 64 : 213-223
Lorant, J., Saury, C., Schleder, C., Robriquet, F., Lieubeau, B., Negroni, E., Leroux, I., Chabrand, L., Viau, S., Babarit, C., Ledevin, M., Dubreil, L., Hamel, A., Magot, A., Thorin, C., Guevel, L., Delorme, B., Pereon, Y., Butler-Browne, G., Mouly, V., Rouger, K. :
Skeletal Muscle Regenerative Potential of Human MuStem Cells following Transplantation into Injured Mice Muscle Mol Ther, 2017 ; (SP) :
Cardas, R., Iliescu, C., Butoianu, N., Seferian, A., Gataullina, S., Gargaun, E., Nectoux, J., Bienvenu, T., Craiu, D., Gidaro, T., Servais, L. :
DMD and West syndrome Neuromuscul Disord, 2017 ; (SP) :
Santos-Zas, I., Cid-Diaz, T., Gonzalez-Sanchez, J., Gurriaran-Rodriguez, U., Seoane-Mosteiro, C., Porteiro, B., Nogueiras, R., Casabiell, X., Luis Relova, J., Gallego, R., Mouly, V., Pazos, Y., Camina, J. P. :
Obestatin controls skeletal muscle fiber-type determination Sci Rep, 2017 ; 7 (1) : 2137
Lattanzi, A, Duguez, S, Moiani, A, Izmiryan, A, Barbon, E, Martin, S, Mamchaoui, K, Mouly, V, Bernardi, F, Mavilio, F, Bovolenta, M :
Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System Molecular Therapy - Nucleic Acids, 2017 ; 7 (6) : 11-19
Pines, M., Levi, O., Genin, O., Lavy, A., Angelini, C., Allamand, V., Halevy, O. :
Elevated Expression of Moesin in Muscular Dystrophies Am J Pathol, 2017 ; 187 (3) : 654-664
Stemmerik, M. G., Madsen, K. L., Laforet, P., Buch, A. E., Vissing, J. :
Muscle glycogen synthesis and breakdown are both impaired in glycogenin-1 deficiency Neurology, 2017 ; (SP) :
Byrne, B. J., Geberhiwot, T., Barshop, B. A., Barohn, R., Hughes, D., Bratkovic, D., Desnuelle, C., Laforet, P., Mengel, E., Roberts, M., Haroldsen, P., Reilley, K., Jayaram, K., Yang, K., Walsh, L., P. O. M. Investigators :
A study on the safety and efficacy of reveglucosidase alfa in patients with late-onset Pompe disease Orphanet J Rare Dis, 2017 ; 12 (1) : 144
Meyer, A., Laverny, G., Allenbach, Y., Grelet, E., Ueberschlag, V., Echaniz-Laguna, A., Lannes, B., Alsaleh, G., Charles, A. L., Singh, F., Zoll, J., Lonsdorfer, E., Maurier, F., Boyer, O., Gottenberg, J. E., Nicot, A. S., Laporte, J., Benveniste, O., Metzger, D., Sibilia, J., Geny, B. :
IFN-beta-induced reactive oxygen species and mitochondrial damage contribute to muscle impairment and inflammation maintenance in dermatomyositis Acta Neuropathol, 2017 ; (SP) :