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
Publications (1181)
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
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
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
A new Centronuclear Myopathy phenotype due to a novel Dynamin 2 mutation. Neurology, 2009 ; 72 (1) : 93-95
Eymard, B, Hantaï, D :
Syndromes myasthéniques congénitaux : phénotype et physiopathologie Les Cahiers de Myologie, 2009 ; (1) : 26-37
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
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
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
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study Acta Neuropathol, 2009 ; 117 (3) : 293-307
Héron, D, Gargiulo, M :
Tests génétiques et médecine prédictive : quels enjeux ? Laennec, 2009 ; 3 : 21-38
Tests génétiques et médecine prédictive : quels enjeux ? Laennec, 2009 ; 3 : 21-38
Mulders, S. A., van den Broek, W. J., Wheeler, T. M., Croes, H. J., van Kuik-Romeijn, P., de Kimpe, S. J., Furling, D., Platenburg, G. J., Gourdon, G., Thornton, C. A., Wieringa, B., Wansink, D. G. :
Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy Proc Natl Acad Sci U S A, 2009 ; 106 (33) : 13915-20
Triplet-repeat oligonucleotide-mediated reversal of RNA toxicity in myotonic dystrophy Proc Natl Acad Sci U S A, 2009 ; 106 (33) : 13915-20
