Publications (1181)

Wray, D. W., Nishiyama, S. K., Monnet, A., Wary, C., Duteil, S., Carlier, P. G., Richardson, R. S. :
Multiparametric NMR-based assessment of skeletal muscle perfusion and metabolism during exercise in elderly persons: preliminary findings J Gerontol A Biol Sci Med Sci, 2009 ; 64 (9) : 968-74
Allenbach, Y., Solly, S., Gregoire, S., Dubourg, O., Salomon, B., Butler-Browne, G., Musset, L., Herson, S., Klatzmann, D., Benveniste, O. :
Role of regulatory T cells in a new mouse model of experimental autoimmune myositis Am J Pathol, 2009 ; 174 (3) : 989-98
Dimitrova, N. A., Arabadzhiev, T. I., Hogrel, J. Y., Dimitrov, G. V. :
Fatigue analysis of interference EMG signals obtained from biceps brachii during isometric voluntary contraction at various force levels J Electromyogr Kinesiol, 2009 ; 19 (2) : 252-8
Krahn, M., Beroud, C., Labelle, V., Nguyen, K., Bernard, R., Bassez, G., Figarella-Branger, D., Fernandez, C., Bouvenot, J., Richard, I., Ollagnon-Roman, E., Bevilacqua, J. A., Salvo, E., Attarian, S., Chapon, F., Pellissier, J. F., Pouget, J., Hammouda el, H., Laforet, P., Urtizberea, J. A., Eymard, B., Leturcq, F., Levy, N. :
Analysis of the DYSF mutational spectrum in a large cohort of patients Hum Mutat, 2009 ; 30 (2) : E345-75
Ramachandran, N., Munteanu, I., Wang, P., Aubourg, P., Rilstone, J. J., Israelian, N., Naranian, T., Paroutis, P., Guo, R., Ren, Z. P., Nishino, I., Chabrol, B., Pellissier, J. F., Minetti, C., Udd, B., Fardeau, M., Tailor, C. S., Mahuran, D. J., Kissel, J. T., Kalimo, H., Levy, N., Manolson, M. F., Ackerley, C. A., Minassian, B. A. :
VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification Cell, 2009 ; 137 (2) : 235-46
Bitoun, M, Bevilacqua, J A, Eymard, B, Prudhon, B, Fardeau, M, Guicheney, P, Romero, N B :
A new Centronuclear Myopathy phenotype due to a novel Dynamin 2 mutation. Neurology, 2009 ; 72 (1) : 93-95
Eymard, B, HantaĂŻ, D :
Syndromes myasthéniques congénitaux : phénotype et physiopathologie Les Cahiers de Myologie, 2009 ; (1) : 26-37
Makri, S., Clarke, N. F., Richard, P., Maugenre, S., Demay, L., Bonne, G., Guicheney, P. :
Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy Neuromuscul Disord, 2009 ; 19 (1) : 26-8
Thornell, L. E., Lindstom, M., Renault, V., Klein, A., Mouly, V., Ansved, T., Butler-Browne, G., Furling, D. :
Satellite Cell Dysfunction Contributes to the Progressive Muscle Atrophy in Myotonic Dystrophy Type 1 Neuropathol Appl Neurobiol, 2009 ; 35 (6) : 603-613
Claeys, K. G., van der Ven, P. F., Behin, A., Stojkovic, T., Eymard, B., Dubourg, O., Laforet, P., Faulkner, G., Richard, P., Vicart, P., Romero, N. B., Stoltenburg, G., Udd, B., Fardeau, M., Voit, T., Furst, D. O. :
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Acta Neuropathol, 2009 ; 117 (3) : 293-307