Barberi, L., Scicchitano, B. M., De Rossi, M., Bigot, A., Duguez, S., Wielgosik, A., Stewart, C., McPhee, J., Conte, M., Narici, M., Franceschi, C., Mouly, V., Butler-Browne, G., Musaro, A. : 
						Age-dependent alteration in muscle regeneration: the critical role of tissue niche
						Biogerontology, 2013 ; 14 (3) : 273-292											
		
					
				Publications (1184)
												Desdouits, M., Munier, S., Prevost, M. C., Jeannin, P., Butler-Browne, G., Ozden, S., Gessain, A., Van Der Werf, S., Naffakh, N., Ceccaldi, P. E. : 
Productive Infection of Human Skeletal Muscle Cells by Pandemic and Seasonal Influenza A(H1N1) Viruses PLoS ONE, 2013 ; 8 (11) : e79628
		
					
				Productive Infection of Human Skeletal Muscle Cells by Pandemic and Seasonal Influenza A(H1N1) Viruses PLoS ONE, 2013 ; 8 (11) : e79628
												Foley, A. R., Quijano-Roy, S., Collins, J., Straub, V., McCallum, M., Deconinck, N., Mercuri, E., Pane, M., D'Amico, A., Bertini, E., North, K., Ryan, M. M., Richard, P., Allamand, V., Hicks, D., Lamande, S., Hu, Y., Gualandi, F., Auh, S., Muntoni, F., Bonnemann, C. G. : 
Natural history of pulmonary function in collagen VI-related myopathies Brain, 2013 ; 136 (Pt 12) : 3625-33
		
					
				Natural history of pulmonary function in collagen VI-related myopathies Brain, 2013 ; 136 (Pt 12) : 3625-33
												Bijlsma, A. Y., Meskers, M. C., Molendijk, M., Westendorp, R. G., Sipila, S., Stenroth, L., Sillanpaa, E., McPhee, J. S., Jones, D. A., Narici, M., Gapeyeva, H., Paasuke, M., Seppet, E., Voit, T., Barnouin, Y., Hogrel, J. Y., Butler-Browne, G., Maier, A. B. : 
Diagnostic measures for sarcopenia and bone mineral density Osteoporos Int, 2013 ; 24 (10) : 2681-91
		
					
				Diagnostic measures for sarcopenia and bone mineral density Osteoporos Int, 2013 ; 24 (10) : 2681-91
												Zhou, H., Rokach, O., Feng, L., Munteanu, I., Mamchaoui, K., Wilmshurst, J. M., Sewry, C., Manzur, A. Y., Pillay, K., Mouly, V., Duchen, M., Jungbluth, H., Treves, S., Muntoni, F. : 
RYR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling Hum Mutat, 2013 ; 34 (7) : 986-996
		
					
				RYR1 Deficiency in Congenital Myopathies Disrupts Excitation-Contraction Coupling Hum Mutat, 2013 ; 34 (7) : 986-996
												Cirak, S., Foley, A. R., Herrmann, R., Willer, T., Yau, S., Stevens, E., Torelli, S., Brodd, L., Kamynina, A., Vondracek, P., Roper, H., Longman, C., Korinthenberg, R., Marrosu, G., Nurnberg, P., Michele, D. E., Plagnol, V., Hurles, M., Moore, S. A., Sewry, C. A., Campbell, K. P., Voit, T., Muntoni, F. : 
ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies Brain, 2013 ; 136 (Pt 1) : 269-281
		
					
				ISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies Brain, 2013 ; 136 (Pt 1) : 269-281
												Pakula, A., Schneider, J., Janke, J., Zacharias, U., Schulz, H., Hubner, N., Mahler, A., Spuler, A., Spuler, S., Carlier, P. G., Boschmann, M. : 
Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1) PLoS ONE, 2013 ; 8 (9) : e73573
		
					
				Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1) PLoS ONE, 2013 ; 8 (9) : e73573
												Perrin, L., Feasson, L., Furby, A., Laforet, P., Petit, F. M., Gautheron, V., Chabrier, S. : 
PNPLA2 mutation: A paediatric case with early onset but indolent course Neuromuscul Disord, 2013 ; 23 (12) : 986-91
		
					
				PNPLA2 mutation: A paediatric case with early onset but indolent course Neuromuscul Disord, 2013 ; 23 (12) : 986-91
												Bucher, T., Colle, M. A., Wakeling, E., Dubreil, L., Fyfe, J., Briot-Nivard, D., Maquigneau, M., Raoul, S., Cherel, Y., Astord, S., Duque, S., Marais, T., Voit, T., Moullier, P., Barkats, M., Joussemet, B. : 
scAAV9 Intracisternal Delivery Results in Efficient Gene Transfer to the Central Nervous System of a Feline Model of Motor Neuron Disease Hum Gene Ther, 2013 ; 24 (7) : 670-682
		
					
				scAAV9 Intracisternal Delivery Results in Efficient Gene Transfer to the Central Nervous System of a Feline Model of Motor Neuron Disease Hum Gene Ther, 2013 ; 24 (7) : 670-682
												Thuault, S., Hayashi, S., Lagirand-Cantaloube, J., Plutoni, C., Comunale, F., Delattre, O., Relaix, F., Gauthier-Rouviere, C. : 
P-cadherin is a direct PAX3-FOXO1A target involved in alveolar rhabdomyosarcoma aggressiveness Oncogene, 2013 ; 32 (15) : 1876-87
		
					
				P-cadherin is a direct PAX3-FOXO1A target involved in alveolar rhabdomyosarcoma aggressiveness Oncogene, 2013 ; 32 (15) : 1876-87
