Calderon, J., Bonnet, D., Pinabiaux, C., Jambaque, I., Angeard, N. :
Use of early remedial services in children with transposition of the great arteries
J Pediatr, 2013 ; 163 (4) : 1105-10
Publications (1184)
Osorio, D. S., Gomes, E. R. :
The contemporary nucleus: a trip down memory lane Biol Cell, 2013 ; 105 (9) : 430-41
The contemporary nucleus: a trip down memory lane Biol Cell, 2013 ; 105 (9) : 430-41
Romero, N. B., Sandaradura, S. A., Clarke, N. F. :
Recent advances in nemaline myopathy Curr Opin Neurol, 2013 ; 26 (5) : 519-26
Recent advances in nemaline myopathy Curr Opin Neurol, 2013 ; 26 (5) : 519-26
Lorain, S, Peccate, C, Le Hir, M, Griffith, G, Philippi, S, Précigout, G, Mamchaoui, K, Jollet, A, Voit, T, Garcia, L :
Dystrophin rescue by trans-splicing: a strategy for DMD genotypes not eligible for exon skipping approaches Nucleic Acids Res, 2013 ; 41 (17) : 8391-402
Dystrophin rescue by trans-splicing: a strategy for DMD genotypes not eligible for exon skipping approaches Nucleic Acids Res, 2013 ; 41 (17) : 8391-402
Raz, V., Butler-Browne, G., van Engelen, B., Brais, B. :
191st ENMC International Workshop: Recent advances in oculopharyngeal muscular dystrophy research: From bench to bedside 8-10 June 2012, Naarden, The Netherlands Neuromuscul Disord, 2013 ; 23 (6) : 516-523
191st ENMC International Workshop: Recent advances in oculopharyngeal muscular dystrophy research: From bench to bedside 8-10 June 2012, Naarden, The Netherlands Neuromuscul Disord, 2013 ; 23 (6) : 516-523
Barbash, I. M., Cecchini, S., Faranesh, A. Z., Virag, T., Li, L., Yang, Y., Hoyt, R. F., Kornegay, J. N., Bogan, J. R., Garcia, L., Lederman, R. J., Kotin, R. M. :
MRI roadmap-guided transendocardial delivery of exon-skipping recombinant adeno-associated virus restores dystrophin expression in a canine model of Duchenne muscular dystrophy Gene Ther, 2013 ; 20 (3) : 274-82
MRI roadmap-guided transendocardial delivery of exon-skipping recombinant adeno-associated virus restores dystrophin expression in a canine model of Duchenne muscular dystrophy Gene Ther, 2013 ; 20 (3) : 274-82
Ben Ammar, A., Soltanzadeh, P., Bauche, S., Richard, P., Goillot, E., Herbst, R., Gaudon, K., Huze, C., Schaeffer, L., Yamanashi, Y., Higuchi, O., Taly, A., Koenig, J., Leroy, J. P., Hentati, F., Najmabadi, H., Kahrizi, K., Ilkhani, M., Fardeau, M., Eymard, B., Hantai, D. :
A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia + Correction (PlosOne 2013 8(9)) PLoS ONE, 2013 ; 8 (1) : e53826
A Mutation Causes MuSK Reduced Sensitivity to Agrin and Congenital Myasthenia + Correction (PlosOne 2013 8(9)) PLoS ONE, 2013 ; 8 (1) : e53826
Schoindre, Y., Benveniste, O., Costedoat-Chalumeau, N. :
Vitamine D et auto-immunite Presse Med, 2013 ; 42 (10) : 1358-63
Vitamine D et auto-immunite Presse Med, 2013 ; 42 (10) : 1358-63
Gayan-Ramirez, G. :
Ventilator-induced diaphragm dysfunction: time for (contr)action ! Eur Respir J, 2013 ; 42 (1) : 12-15
Ventilator-induced diaphragm dysfunction: time for (contr)action ! Eur Respir J, 2013 ; 42 (1) : 12-15
Penisson-Besnier, I., Allamand, V., Beurrier, P., Martin, L., Schalkwijk, J., van Vlijmen-Willems, I., Gartioux, C., Malfait, F., Syx, D., Macchi, L., Marcorelles, P., Arbeille, B., Croue, A., De Paepe, A., Dubas, F. :
Compound heterozygous mutations of the TNXB gene cause primary myopathy Neuromuscul Disord, 2013 ; 23 (8) : 664-9
Compound heterozygous mutations of the TNXB gene cause primary myopathy Neuromuscul Disord, 2013 ; 23 (8) : 664-9
