Baraibar, M. A., Gueugneau, M., Duguez, S., Butler-Browne, G., Bechet, D., Friguet, B. :
Expression and modification proteomics during skeletal muscle ageing
Biogerontology, 2013 ; 4 (3) : 339-352
Publications (1184)
Moraux, A., Canal, A., Ollivier, G., Ledoux, I., Doppler, V., Payan, C., Hogrel, J. Y. :
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years BMC Musculoskelet Disord, 2013 ; 14 : 104
Ankle dorsi- and plantar-flexion torques measured by dynamometry in healthy subjects from 5 to 80 years BMC Musculoskelet Disord, 2013 ; 14 : 104
Wahbi, K., Behin, A., Becane, H. M., Leturcq, F., Cossee, M., Laforet, P., Stojkovic, T., Carlier, P., Toussaint, M., Gaxotte, V., Cluzel, P., Eymard, B., Duboc, D. :
Dilated cardiomyopathy in patients with mutations in anoctamin 5 Int J Cardiol, 2013 ; 168 (1) : 76-9
Dilated cardiomyopathy in patients with mutations in anoctamin 5 Int J Cardiol, 2013 ; 168 (1) : 76-9
Mercier, S., Toutain, A., Toussaint, A., Raynaud, M., de Barace, C., Marcorelles, P., Pasquier, L., Blayau, M., Espil, C., Parent, P., Journel, H., Lazaro, L., Andoni Urtizberea, J., Moerman, A., Faivre, L., Eymard, B., Maincent, K., Gherardi, R., Chaigne, D., Ben Yaou, R., Leturcq, F., Chelly, J., Desguerre, I. :
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age Eur J Hum Genet, 2013 ; 21 (8) : 855-863
Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age Eur J Hum Genet, 2013 ; 21 (8) : 855-863
Gallais, B., Gargiulo, M., Montreuil, M., Eymard, B. :
La fatigue dans la dystrophie myotonique de Steinert : revue de la littérature et voies de recherche Annales médico-psychologiques, 2013 ; 171 (2) : 83-88
La fatigue dans la dystrophie myotonique de Steinert : revue de la littérature et voies de recherche Annales médico-psychologiques, 2013 ; 171 (2) : 83-88
Jacquin, A., Rouaud, O., Soichot, P., Bejot, Y., Dygai-Cochet, I., Sarazin, M., Stojkovic, T., Lemesle-Martin, M., Giroud, M., Moreau, T. :
Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family Case Rep Neurol, 2013 ; 5 (3) : 187-94
Psychiatric Presentation of Frontotemporal Dementia Associated with Inclusion Body Myopathy due to the VCP Mutation (R155H) in a French Family Case Rep Neurol, 2013 ; 5 (3) : 187-94
Malfatti, E., Schaeffer, U., Chapon, F., Yang, Y., Eymard, B., Xu, R., Laporte, J., Romero, N. B. :
Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene Neuromuscul Disord, 2013 ; 23 (12) : 992-7
Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 gene Neuromuscul Disord, 2013 ; 23 (12) : 992-7
Mearini, G., Stimpel, D., Kramer, E., Geertz, B., Braren, I., Gedicke-Hornung, C., Precigout, G., Muller, O. J., Katus, H. A., Eschenhagen, T., Voit, T., Garcia, L., Lorain, S., Carrier, L. :
Repair of Mybpc3 mRNA by 5′-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy Mol Ther Nucleic Acids, 2013 ; 2 : e102
Repair of Mybpc3 mRNA by 5′-trans-splicing in a Mouse Model of Hypertrophic Cardiomyopathy Mol Ther Nucleic Acids, 2013 ; 2 : e102
Relaix, F., Demignon, J., Laclef, C., Pujol, J., Santolini, M., Niro, C., Lagha, M., Rocancourt, D., Buckingham, M., Maire, P. :
Six homeoproteins directly activate myod expression in the gene regulatory networks that control early myogenesis PLoS Genet, 2013 ; 9 (4) : e1003425
Six homeoproteins directly activate myod expression in the gene regulatory networks that control early myogenesis PLoS Genet, 2013 ; 9 (4) : e1003425
Masat, E., Pavani, G., Mingozzi, F. :
Humoral immunity to AAV vectors in gene therapy: challenges and potential solutions Discov Med, 2013 ; 15 (85) : 379-89
Humoral immunity to AAV vectors in gene therapy: challenges and potential solutions Discov Med, 2013 ; 15 (85) : 379-89
