Publications (1181)

Berrih-Aknin, S., Souroujon, M. C. :
Myasthenia gravis: Special issue Autoimmun Rev, 2013 ; 12 (9) : 861-2
Finsterer, J., Stollberger, C., Wahbi, K. :
Cardiomyopathy in neurological disorders Cardiovasc Pathol, 2013 ; 22 (5) : 389-400
Gargiulo, M., Herson, A., Michon, C. C., Hogrel, J. Y., Doppler, V., Laloui, K., Herson, S., Payan, C., Eymard, B., Laforet, P. :
Attitudes and expectations of patients with neuromuscular diseases about their participation in a clinical trial Rev Neurol (Paris), 2013 ; 169 (8-9) : 670-676
Stohr, A., Friedrich, F. W., Flenner, F., Geertz, B., Eder, A., Schaaf, S., Hirt, M. N., Uebeler, J., Schlossarek, S., Carrier, L., Hansen, A., Eschenhagen, T. :
Contractile abnormalities and altered drug response in engineered heart tissue from Mybpc3-targeted knock-in mice J Mol Cell Cardiol, 2013 ; 63 : 189-198
Arimura, T., Onoue, K., Takahashi-Tanaka, Y., Ishikawa, T., Kuwahara, M., Setou, M., Shigenobu, S., Yamaguchi, K., Bertrand, A. T., Machida, N., Takayama, K., Fukusato, M., Tanaka, R., Somekawa, S., Nakano, T., Yamane, Y., Kuba, K., Imai, Y., Saito, Y., Bonne, G., Kimura, A. :
Nuclear accumulation of androgen receptor in gender difference of dilated cardiomyopathy due to lamin A/C mutations Cardiovasc Res, 2013 ; 99 (3) : 382-94
Chort, A., Alves, S., Marinello, M., Dufresnois, B., Dornbierer, J. G., Tesson, C., Latouche, M., Baker, D. P., Barkats, M., El Hachimi, K. H., Ruberg, M., Janer, A., Stevanin, G., Brice, A., Sittler, A. :
Interferon beta induces clearance of mutant ataxin 7 and improves locomotion in SCA7 knock-in mice Brain, 2013 ; 136 (Pt 6) : 1732-1745
Schirwis, E., Agbulut, O., Vadrot, N., Mouisel, E., Hourde, C., Bonnieu, A., Butler-Browne, G., Amthor, H., Ferry, A. :
The beneficial effect of myostatin deficiency on maximal muscle force and power is attenuated with age Exp Gerontol, 2013 ; 48 (2) : 183-190
Mayhew, A., Mazzone, E. S., Eagle, M., Duong, T., Ash, M., Decostre, V., Vandenhauwe, M., Klingels, K., Florence, J., Main, M., Bianco, F., Henrikson, E., Servais, L., Campion, G., Vroom, E., Ricotti, V., Goemans, N., McDonald, C., Mercuri, E. :
Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy Dev Med Child Neurol, 2013 ; 55 (11) : 1038-45
Aure, K., Dubourg, O., Jardel, C., Clarysse, L., Sternberg, D., Fournier, E., Laforet, P., Streichenberger, N., Petiot, P., Gervais-Bernard, H., Vial, C., Bedat-Millet, A. L., Drouin-Garraud, V., Bouillaud, F., Vandier, C., Fontaine, B., Lombes, A. :
Episodic weakness due to mitochondrial DNA MT-ATP6/8 mutations Neurology, 2013 ; 81 (21) : 1810-8
Shichiji, M, Biancalana, V, Fardeau, M, Hogrel, J Y, Osawa, M, Laporte, J, Romero, N B :
Extensive morphological and immunohistochemical characterization in myotubular myopathy Brain Behavior, 2013 ; 3 (4) : 476-486