Allenbach, Y, Guiguet, M, Rigolet, A, Marie, I, Hachulla, E, Drouot, L, Jouen, F, Jacquot, S, Mariampillai, K, Musset, L, Grenier, P, Devilliers, H, Hij, A, Boyer, O, Herson, S, Benveniste, O :
Efficacy of Rituximab in Refractory Inflammatory Myopathies Associated with Anti- Synthetase Auto-Antibodies: an Open-Label, Phase II Trial
PLoS ONE, 2015 ; (SP) :
Publications (1184)
Maurer, M., Bougoin, S., Feferman, T., Frenkian, M., Bismuth, J., Mouly, V., Clairac, G., Tzartos, S., Fadel, E., Eymard, B., Fuchs, S., Souroujon, M. C., Berrih-Aknin, S. :
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
IL-6 and Akt are involved in muscular pathogenesis in myasthenia gravis Acta Neuropathol Commun, 2015 ; 3 (1) : 1
Gali Ramamoorthy, T., Laverny, G., Schlagowski, A. I., Zoll, J., Messaddeq, N., Bornert, J. M., Panza, S., Ferry, A., Geny, B., Metzger, D. :
The transcriptional coregulator PGC-1beta controls mitochondrial function and anti-oxidant defence in skeletal muscles Nat Commun, 2015 ; 6 : 10210
The transcriptional coregulator PGC-1beta controls mitochondrial function and anti-oxidant defence in skeletal muscles Nat Commun, 2015 ; 6 : 10210
Béhin, A., Tiberghien, D., Babonneau, M. L., Brocq, H., Michon, C. C., Gargiulo, M., Réveillère, C. :
Mise au point : Urgences psychiatriques et traitements psychotropes dans les maladies neuromusculaires Anesthésie & Réanimation, 2015 ; 1 (suppl 1) : 47-52
Mise au point : Urgences psychiatriques et traitements psychotropes dans les maladies neuromusculaires Anesthésie & Réanimation, 2015 ; 1 (suppl 1) : 47-52
Chartier, A., Klein, P., Pierson, S., Barbezier, N., Gidaro, T., Casas, F., Carberry, S., Dowling, P., Maynadier, L., Bellec, M., Oloko, M., Jardel, C., Moritz, B., Dickson, G., Mouly, V., Ohlendieck, K., Butler-Browne, G., Trollet, C., Simonelig, M. :
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
Mitochondrial dysfunction reveals the role of mRNA poly(A) tail regulation in oculopharyngeal muscular dystrophy pathogenesis PLoS Genet, 2015 ; 11 (3) : e1005092
Preisler, N., Laforet, P., Madsen, K. L., Prahm, K. P., Hedermann, G., Vissing, C. R., Galbo, H., Vissing, J. :
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III Neurology, 2015 ; 84 (17) : 1767-1771
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III Neurology, 2015 ; 84 (17) : 1767-1771
Meliani, A., Leborgne, C., Triffault, S., Jeanson-Leh, L., Veron, P., Mingozzi, F. :
Determination of anti-adeno-associated virus vector neutralizing antibody titer with an in vitro reporter system Hum Gene Ther Methods, 2015 ; 26 (2) : 45-53
Determination of anti-adeno-associated virus vector neutralizing antibody titer with an in vitro reporter system Hum Gene Ther Methods, 2015 ; 26 (2) : 45-53
Blondelle, J., Ohno, Y., Gache, V., Guyot, S., Storck, S., Blanchard-Gutton, N., Barthelemy, I., Walmsley, G., Rahier, A., Gadin, S., Maurer, M., Guillaud, L., Prola, A., Ferry, A., Aubin-Houzelstein, G., Demarquoy, J., Relaix, F., Piercy, R. J., Blot, S., Kihara, A., Tiret, L., Pilot-Storck, F. :
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth J Mol Cell Biol, 2015 ; 7 (5) : 429-40
HACD1, a regulator of membrane composition and fluidity, promotes myoblast fusion and skeletal muscle growth J Mol Cell Biol, 2015 ; 7 (5) : 429-40
Yaou, R. B., De Sandre-Giovannoli, A., Leturcq, F., Levy, N., Bonne, G. :
Premiere reunion franco-italienne des laminopathies et autres pathologies liees a l’enveloppe nucleaire Med Sci (Paris), 2015 ; 31 Spec No 3 : 39-40
Premiere reunion franco-italienne des laminopathies et autres pathologies liees a l’enveloppe nucleaire Med Sci (Paris), 2015 ; 31 Spec No 3 : 39-40
Cacheux, M., Blum, A., Sebastien, M., Wozny, A. S., Brocard, J., Mamchaoui, K., Mouly, V., Roux-Buisson, N., Rendu, J., Monnier, N., Krivosic, R., Allen, P., Lacour, A., Lunardi, J., Faure, J., Marty, I. :
Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein J Neuromuscul Dis, 2015 ; 2 (4) : 421-432
Functional Characterization of a Central Core Disease RyR1 Mutation (p.Y4864H) Associated with Quantitative Defect in RyR1 Protein J Neuromuscul Dis, 2015 ; 2 (4) : 421-432
