Geier, C, Schultze-Bahr, E, Bonne, G. :
Guiding the molecular diagnosis of hypertrophic cardiomyopathy
J Thorac Cardiovasc Surg, 2012 ; 143 (5) : 1234
Publications (1181)
Marston, S., Copeland, O., Gehmlich, K., Schlossarek, S., Carrrier, L. :
How do MYBPC3 mutations cause hypertrophic cardiomyopathy? J Muscle Res Cell Motil, 2012 ; 33 : 75-80
How do MYBPC3 mutations cause hypertrophic cardiomyopathy? J Muscle Res Cell Motil, 2012 ; 33 : 75-80
Ucar, A., Gupta, S. K., Fiedler, J., Erikci, E., Kardasinski, M., Batkai, S., Dangwal, S., Kumarswamy, R., Bang, C., Holzmann, A., Remke, J., Caprio, M., Jentzsch, C., Engelhardt, S., Geisendorf, S., Glas, C., Hofmann, T. G., Nessling, M., Richter, K., Schiffer, M., Carrier, L., Napp, L. C., Bauersachs, J., Chowdhury, K., Thum, T. :
The miRNA-212/132 family regulates both cardiac hypertrophy and cardiomyocyte autophagy Nat Commun, 2012 ; 3 : 1078
The miRNA-212/132 family regulates both cardiac hypertrophy and cardiomyocyte autophagy Nat Commun, 2012 ; 3 : 1078
Castets, P., Lescure, A., Guicheney, P., Allamand, V. :
Selenoprotein N in skeletal muscle: from diseases to function J Mol Med (Berl), 2012 ; 90 (10) : 1095-1107
Selenoprotein N in skeletal muscle: from diseases to function J Mol Med (Berl), 2012 ; 90 (10) : 1095-1107
Herson, S., Hentati, F., Rigolet, A., Behin, A., Romero, N. B., Leturcq, F., Laforet, P., Maisonobe, T., Amouri, R., Haddad, H., Audit, M., Montus, M., Masurier, C., Gjata, B., Georger, C., Cherai, M., Carlier, P., Hogrel, J. Y., Herson, A., Allenbach, Y., Lemoine, F. M., Klatzmann, D., Sweeney, H. L., Mulligan, R. C., Eymard, B., Caizergues, D., Voit, T., Benveniste, O. :
A phase I trial of adeno-associated virus serotype 1-gamma-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C Brain, 2012 ; 135 (Pt 2) : 483-492
A phase I trial of adeno-associated virus serotype 1-gamma-sarcoglycan gene therapy for limb girdle muscular dystrophy type 2C Brain, 2012 ; 135 (Pt 2) : 483-492
Ochala, J., Gokhin, D. S., Penisson-Besnier, I., Quijano-Roy, S., Monnier, N., Lunardi, J., Romero, N. B., Fowler, V. M. :
Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms Hum Mol Genet, 2012 ; 21 (20) : 4473-85
Congenital myopathy-causing tropomyosin mutations induce thin filament dysfunction via distinct physiological mechanisms Hum Mol Genet, 2012 ; 21 (20) : 4473-85
Wakeling, E. N., Joussemet, B., Costiou, P., Fanuel, D., Moullier, P., Barkats, M., Fyfe, J. C. :
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of SMA J Comp Neurol, 2012 ; 520 (8) : 1737-1750
Failure of lower motor neuron radial outgrowth precedes retrograde degeneration in a feline model of SMA J Comp Neurol, 2012 ; 520 (8) : 1737-1750
Dowling, J. J., Arbogast, S., Hur, J., Nelson, D. D., McEvoy, A., Waugh, T., Marty, I., Lunardi, J., Brooks, S. V., Kuwada, J. Y., Ferreiro, A. :
Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy Brain, 2012 ; 135 (Pt 4) : 1115-1127
Oxidative stress and successful antioxidant treatment in models of RYR1-related myopathy Brain, 2012 ; 135 (Pt 4) : 1115-1127
Lacourpaille, L., Hug, F., Bouillard, K., Hogrel, J. Y., Nordez, A. :
Supersonic shear imaging provides a reliable measurement of resting muscle shear elastic modulus Physiol Meas, 2012 ; 33 (3) : N19-28
Supersonic shear imaging provides a reliable measurement of resting muscle shear elastic modulus Physiol Meas, 2012 ; 33 (3) : N19-28
Rigolet, A., Musset, L., Dubourg, O., Maisonobe, T., Grenier, P., Charuel, J. L., Behin, A., Herson, S., Amoura, Z., Benveniste, O. :
Inflammatory myopathies with anti-ku antibodies: a prognosis dependent on associated lung disease Medicine (Baltimore), 2012 ; 91 (2) : 95-102
Inflammatory myopathies with anti-ku antibodies: a prognosis dependent on associated lung disease Medicine (Baltimore), 2012 ; 91 (2) : 95-102
