Meune, C., Wahbi, K., Gobeaux, C., Duboc, D., Pecker, F., Bonne, G. :
N-terminal Pro brain natriuretic peptide is a reliable biomarker of reduced myocardial contractility in patients with lamin A/C gene mutations
Int J Cardiol, 2011 ; 151 (2) : 160-3
Publications (1184)
Zuily, S., Chenevier-Gobeaux, C., Claessens, Y. E., Wahbi, K., Weber, S., Meune, C. :
High diagnostic performance of a high-sensitivity cardiac troponin T assay in patients with suspected acute coronary syndrome Int J Cardiol, 2011 ; 146 (1) : 115-116
High diagnostic performance of a high-sensitivity cardiac troponin T assay in patients with suspected acute coronary syndrome Int J Cardiol, 2011 ; 146 (1) : 115-116
Carmignac, V., Svensson, M., Korner, Z., Elowsson, L., Matsumura, C., Gawlik, K. I., Allamand, V., Durbeej, M. :
Autophagy is increased in laminin {alpha}2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A Hum Mol Genet, 2011 ; 20 (24) : 4891-4902
Autophagy is increased in laminin {alpha}2 chain-deficient muscle and its inhibition improves muscle morphology in a mouse model of MDC1A Hum Mol Genet, 2011 ; 20 (24) : 4891-4902
Khattar, P., Friedrich, F. W., Bonne, G., Carrier, L., Eschenhagen, T., Evans, S. M., Schwartz, K., Fiszman, M. Y., Vilquin, J. T. :
Distinction between two populations of islet-1-positive cells in hearts of different murine strains Stem Cells Dev, 2011 ; 20 (6) : 1043-52
Distinction between two populations of islet-1-positive cells in hearts of different murine strains Stem Cells Dev, 2011 ; 20 (6) : 1043-52
Rederstorff, M., Castets, P., Arbogast, S., Laine, J., Vassilopoulos, S., Beuvin, M., Dubourg, O., Vignaud, A., Ferry, A., Krol, A., Allamand, V., Guicheney, P., Ferreiro, A., Lescure, A. :
Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy PLoS ONE, 2011 ; 6 (8) : e23094
Increased Muscle Stress-Sensitivity Induced by Selenoprotein N Inactivation in Mouse: A Mammalian Model for SEPN1-Related Myopathy PLoS ONE, 2011 ; 6 (8) : e23094
Ben Ammar, A., Petit, F., Alexandri, N., Gaudon, K., Bauche, S., Rouche, A., Gras, D., Fournier, E., Koenig, J., Stojkovic, T., Lacour, A., Petiot, P., Zagnoli, F., Viollet, L., Pellegrini, N., Orlikowski, D., Lazaro, L., Ferrer, X., Stoltenburg, G., Paturneau-Jouas, M., Hentati, F., Fardeau, M., Sternberg, D., Hantai, D., Richard, P., Eymard, B. :
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 J Neurol, 2010 ; 257 (5) : 754-766
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7 J Neurol, 2010 ; 257 (5) : 754-766
Garcin, B., Lenglet, T., Dubourg, O., Mesnage, V., Levy, R. :
Dropped head syndrome as a presenting sign of scleromyositis J Neurol Sci, 2010 ; 292 (1-2) : 101-103
Dropped head syndrome as a presenting sign of scleromyositis J Neurol Sci, 2010 ; 292 (1-2) : 101-103
Muntoni, F., Voit, T :
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009 Neuromuscul Disord, 2010 ; 20 (5) : 355-62
The development of antisense oligonucleotide therapies for Duchenne muscular dystrophy: report on a TREAT-NMD workshop hosted by the European Medicines Agency (EMA), on September 25th 2009 Neuromuscul Disord, 2010 ; 20 (5) : 355-62
Cavalcante, P., Barberis, M., Cannone, M., Baggi, F., Antozzi, C., Maggi, L., Cornelio, F., Barbi, M., Dido, P., Berrih-Aknin, S., Mantegazza, R., Bernasconi, P. :
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravis Neurology, 2010 ; 74 (14) : 1118-26
Detection of poliovirus-infected macrophages in thymus of patients with myasthenia gravis Neurology, 2010 ; 74 (14) : 1118-26
Laforet, P., Doppler, V., Caillaud, C., Laloui, K., Claeys, K. G., Richard, P., Ferreiro, A., Eymard, B. :
Rigid spine syndrome revealing late-onset Pompe disease Neuromuscul Disord, 2010 ; 20 (2) : 128-130
Rigid spine syndrome revealing late-onset Pompe disease Neuromuscul Disord, 2010 ; 20 (2) : 128-130
