Hervier, B., Lambert, M., Hachulla, E., Musset, L., Benveniste, O., Piette, J. C., Amoura, Z., Costedoat-Chalumeau, N. :
Anti-synthetase syndrome positive for anti-isoleucyl-tRNA synthetase antibodies: an unusual case overlapping with systemic sclerosis and Sjogren’s syndrome
Rheumatology (Oxford), 2011 ; 50 (6) : 1175-6
Publications (1181)
Monteilhet, V., Saheb, S., Boutin, S., Leborgne, C., Veron, P., Montus, M. F., Moullier, P., Benveniste, O., Masurier, C. :
A 10 Patient Case Report on the Impact of Plasmapheresis Upon Neutralizing Factors Against Adeno-associated Virus (AAV) Types 1, 2, 6, and 8 Mol Ther, 2011 ; 19 (11) : 2084-91
A 10 Patient Case Report on the Impact of Plasmapheresis Upon Neutralizing Factors Against Adeno-associated Virus (AAV) Types 1, 2, 6, and 8 Mol Ther, 2011 ; 19 (11) : 2084-91
Arbogast, S, Ferreiro, A :
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Selenoproteins and protection against oxidative stress : selenoprotein N as a novel player at the crossroads of redox signalling and calcium homeostasis Antioxid Redox Signal, 2010 ; 12 (7) : 893-904
Durieux, A. C., Vignaud, A., Prudhon, B., Viou, M. T., Beuvin, M., Vassilopoulos, S., Fraysse, B., Ferry, A., Laine, J., Romero, N. B., Guicheney, P., Bitoun, M. :
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
A centronuclear myopathy-dynamin 2 mutation impairs skeletal muscle structure and function in mice Hum Mol Genet, 2010 ; 19 (24) : 4820-4836
Mearini, G., Gedicke, C., Schlossarek, S., Witt, C. C., Kramer, E., Cao, P., Gomes, M. D., Lecker, S. H., Labeit, S., Willis, M. S., Eschenhagen, T., Carrier, L. :
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Atrogin-1 and MuRF1 regulate cardiac MyBP-C levels via different mechanisms Cardiovasc Res, 2010 ; 85 (2) : 357-366
Vuillerot, C., Girardot, F., Payan, C., Fermanian, J., Iwaz, J., De Lattre, C, Berard, C. :
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
Monitoring changes and predicting loss of ambulation in Duchenne muscular dystrophy with the Motor Function Measure Dev Med Child Neurol, 2010 ; 52 (1) : 60-65
Boerio, D., Creange, A., Hogrel, J. Y., Gueguen, A., Bertrand, D., Lefaucheur, J. P. :
Nerve excitability changes after intravenous immunoglobulin infusions in multifocal motor neuropathy and chronic inflammatory demyelinating neuropathy J Neurol Sci, 2010 ; 292 (1-2) : 63-71
Nerve excitability changes after intravenous immunoglobulin infusions in multifocal motor neuropathy and chronic inflammatory demyelinating neuropathy J Neurol Sci, 2010 ; 292 (1-2) : 63-71
Gilardeau, C :
Maladie de Charcot-Marie-Tooth (2ème volet). Traitements Kiné Actualités, 2010 ; 1208 : 18-21
Maladie de Charcot-Marie-Tooth (2ème volet). Traitements Kiné Actualités, 2010 ; 1208 : 18-21
Pietri-Rouxel, F., Gentil, C., Vassilopoulos, S., Baas, D., Mouisel, E., Ferry, A., Vignaud, A., Hourde, C., Marty, I., Schaeffer, L., Voit, T., Garcia, L. :
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis EMBO J, 2010 ; 29 (3) : 643-654
DHPR alpha1S subunit controls skeletal muscle mass and morphogenesis EMBO J, 2010 ; 29 (3) : 643-654
Claeys, K. G., Maisonobe, T., Bohm, J., Laporte, J., Hezode, M., Romero, N. B., Brochier, G., Bitoun, M., Carlier, R. Y., Stojkovic, T. :
Phenotype of a patient with recessive centronuclear myopathy and a novel bin1 mutation Neurology, 2010 ; 74 (6) : 519-521
Phenotype of a patient with recessive centronuclear myopathy and a novel bin1 mutation Neurology, 2010 ; 74 (6) : 519-521
