Rau, F., Freyermuth, F., Fugier, C., Villemin, J. P., Fischer, M. C., Jost, B., Dembele, D., Gourdon, G., Nicole, A., Duboc, D., Wahbi, K., Day, J. W., Fujimura, H., Takahashi, M. P., Auboeuf, D., Dreumont, N., Furling, D., Charlet-Berguerand, N. :
Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy
Nat Struct Mol Biol, 2011 ; 18 (7) : 840-5
Publications (1181)
Dubourg, O., Maisonobe, T., Behin, A., Suominen, T., Raheem, O., Penttila, S., Parton, M., Eymard, B., Dahl, A., Udd, B. :
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient J Neurol, 2011 ; 258 (6) : 1157-1163
A novel MYH7 mutation occurring independently in French and Norwegian Laing distal myopathy families and de novo in one Finnish patient J Neurol, 2011 ; 258 (6) : 1157-1163
Li, K, Hewson, DJ, Duchêne, J, Hogrel, J Y :
Recurrence quantification analysis of sustained sub-maximal grip contractions in patients with various metabolic muscle disorders Biomed Sig Proc Control, 2011 ; 6 (1) : 70-76
Recurrence quantification analysis of sustained sub-maximal grip contractions in patients with various metabolic muscle disorders Biomed Sig Proc Control, 2011 ; 6 (1) : 70-76
Sylvius, N., Bonne, G., Straatman, K., Reddy, T., Gant, T. W., Shackleton, S. :
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy FASEB J, 2011 ; 25 (11) : 3966-78
MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy FASEB J, 2011 ; 25 (11) : 3966-78
Benveniste, O., Guiguet, M., Freebody, J., Dubourg, O., Squier, W., Maisonobe, T., Stojkovic, T., Leite, M. I., Allenbach, Y., Herson, S., Brady, S., Eymard, B., Hilton-Jones, D. :
Long-term observational study of sporadic inclusion body myositis Brain, 2011 ; 134 (Pt 11) : 3176-3184
Long-term observational study of sporadic inclusion body myositis Brain, 2011 ; 134 (Pt 11) : 3176-3184
Granger, B., Gueneau, L., Drouin-Garraud, V., Pedergnana, V., Gagnon, F., Ben Yaou, R., Tezenas du Montcel, S., Bonne, G. :
Modifier locus of the skeletal muscle involvement in Emery-Dreifuss muscular dystrophy Hum Genet, 2011 ; 129 (2) : 149-159
Modifier locus of the skeletal muscle involvement in Emery-Dreifuss muscular dystrophy Hum Genet, 2011 ; 129 (2) : 149-159
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
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
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
