Stojkovic, T, Vissing, J, Petit, F, Piraud, M., Orngreen, M C, Andersen, G, Claeys, K, Wary, C, Hogrel, J Y, Laforet, P :
Muscle Glycogenosis Due to Phosphoglucomutase 1 Deficiency
N Engl J Med, 2009 ; 361 (4) : 425-427
Publications (1181)
Ciron, C., Cressant, A., Roux, F., Raoul, S., Cherel, Y., Hantraye, P., Deglon, N., Schwartz, B., Barkats, M., Heard, J. M., Tardieu, M., Moullier, P., Colle, M. A. :
AAV1-, AAV2- and AAV5-Mediated human alpha-Iduronidase Gene Transfer In The Brain of Nonhuman Primate: Vector Diffusion and Bio Distribution Hum Gene Ther, 2009 ; 20 (4) : 350-360
AAV1-, AAV2- and AAV5-Mediated human alpha-Iduronidase Gene Transfer In The Brain of Nonhuman Primate: Vector Diffusion and Bio Distribution Hum Gene Ther, 2009 ; 20 (4) : 350-360
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
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
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
