Hamidi, S., Levisage, C., Fromes, Y., Isnard, R., Vainchenker, W., Letourneur, D., Norol, F. :
Culture et délivrance au niveau du tissu cardiaque de cardiomyocytes issus de cellules souches embryonnaires humaines au moyen de matrices tridimensionelles poreuses à base de polysaccharides
Archives of Cardiovascular Diseases, 2009 ; 102 (Supplement 1) : S128
Publications (1181)
Muchir, A, Shan, J, Bonne G,, Lehnart, SE, Worman, HJ :
Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins Human Molecular Genetics, 2009 ; 18 (2) : 241-247
Inhibition of extracellular signal-regulated kinase signaling to prevent cardiomyopathy caused by mutation in the gene encoding A-type lamins Human Molecular Genetics, 2009 ; 18 (2) : 241-247
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
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
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
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
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, HantaĂŻ, 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
