Publications (1181)

Herson, S., Hentati, F., Rigolet, A., Behin, A., Romero, N. B., Leturcq, F., Laforet, P., Maisonobe, T., Amouri, R., Haddad, H., Audit, M., Montus, M., Masurier, C., Gjata, B., Georger, C., Cherai, M., Carlier, P., Hogrel, J. Y., Herson, A., Allenbach, Y., Lemoine, F. M., Klatzmann, D., Sweeney, H. L., Mulligan, R. C., Eymard, B., Caizergues, D., Voit, T., Benveniste, O. :
A phase I trial of adeno-associated virus serotype 1-gamma-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C Brain, 2012 ; 135 (Pt 2) : 483-492
Ochala, J., Gokhin, D. S., Penisson-Besnier, I., Quijano-Roy, S., Monnier, N., Lunardi, J., Romero, N. B., Fowler, V. M. :
Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms Hum Mol Genet, 2012 ; 21 (20) : 4473-85
Wakeling, E. N., Joussemet, B., Costiou, P., Fanuel, D., Moullier, P., Barkats, M., Fyfe, J. C. :
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of SMA J Comp Neurol, 2012 ; 520 (8) : 1737-1750
Dowling, J. J., Arbogast, S., Hur, J., Nelson, D. D., McEvoy, A., Waugh, T., Marty, I., Lunardi, J., Brooks, S. V., Kuwada, J. Y., Ferreiro, A. :
Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy Brain, 2012 ; 135 (Pt 4) : 1115-1127
Lacourpaille, L., Hug, F., Bouillard, K., Hogrel, J. Y., Nordez, A. :
Supersonic shear imaging provides a reliable measurement of resting muscle shear elastic modulus Physiol Meas, 2012 ; 33 (3) : N19-28
Rigolet, A., Musset, L., Dubourg, O., Maisonobe, T., Grenier, P., Charuel, J. L., Behin, A., Herson, S., Amoura, Z., Benveniste, O. :
Inflammatory myopathies with anti-ku antibodies: a prognosis dependent on associated lung disease Medicine (Baltimore), 2012 ; 91 (2) : 95-102
Biermann, D., Heilmann, A., Didie, M., Schlossarek, S., Wahab, A., Grimm, M., Romer, M., Reichenspurner, H., Sultan, K. R., Steenpass, A., Ergun, S., Donzelli, S., Carrier, L., Ehmke, H., Zimmermann, W. H., Hein, L., Boger, R. H., Benndorf, R. A. :
Impact of AT2 Receptor Deficiency on Postnatal Cardiovascular Development PLoS ONE, 2012 ; 7 (10) : e47916
Gentil, C, Leturcq, F, Ben Yaou, R, Kaplan, J. C., Laforet, P, Penisson-Besnier, I., Espil-Taris, C, Voit, T, Garcia, L, Piétri-Rouxel, F :
Variable phenotype of delta-45-55 Becker patients correlated to nNOSΌ mislocalization and RYR1 hypernitrosylation. Hum Mol Genet, 2012 ; 21 (15) : 3449-3460
Matsakas, A., Macharia, R., Otto, A., Elashry, M., Mouisel, E., Romanello, V., Sartori, R., Amthor, H., Sandri, M., Narkar, V., Patel, K. :
Exercise-training attenuates the hyper-muscular phenotype and restores skeletal muscle function in the myostatin null mouse Exp Physiol, 2012 ; 97 (1) : 125-140
van der Ploeg, A. T., Barohn, R., Carlson, L., Charrow, J., Clemens, P. R., Hopkin, R. J., Kishnani, P. S., Laforet, P., Morgan, C., Nations, S., Pestronk, A., Plotkin, H., Rosenbloom, B. E., Sims, K. B., Tsao, E. :
Open-label extension study following the Late-Onset Treatment Study (LOTS) of alglucosidase alfa Mol Genet Metab, 2012 ; 107 (3) : 456-461