Eymard, B., Camdessanche, J. P. :
Foreword
Rev Neurol (Paris), 2016 ; 172 (10) : 537-538
Publications (1181)
Beyer, S., Pontis, J., Schirwis, E., Battisti, V., Rudolf, A., Le Grand, F., Ait-Si-Ali, S. :
Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. Erratum: Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. [Cell Discov. 2016] Cell Discov, 2016 ; 2 : 16037
Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. Erratum: Canonical Wnt signalling regulates nuclear export of Setdb1 during skeletal muscle terminal differentiation. [Cell Discov. 2016] Cell Discov, 2016 ; 2 : 16037
Bouchereau, J., Barrot, S. V., Dupre, T., Moore, S. E., Cardas, R., Capri, Y., Gaignard, P., Slama, A., Delanoe, C., de Baulny, H. O., Seta, N., Schiff, M., Servais, L. :
Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants JIMD Rep, 2016 ; :
Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants JIMD Rep, 2016 ; :
Alameddine, H. S., Morgan, J. E. :
Matrix Metalloproteinases and Tissue Inhibitor of Metalloproteinases in Inflammation and Fibrosis of Skeletal Muscles J Neuromuscul Dis, 2016 ; 3 (4) : 455-473
Matrix Metalloproteinases and Tissue Inhibitor of Metalloproteinases in Inflammation and Fibrosis of Skeletal Muscles J Neuromuscul Dis, 2016 ; 3 (4) : 455-473
Ziat, E., Mamchaoui, K., Beuvin, M., Nelson, I., Azibani, F., Spuler, S., Bonne, G., Bertrand, A. T. :
FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy J Neuromuscul Dis, 2016 ; 3 (4) : 497-510
FHL1B Interacts with Lamin A/C and Emerin at the Nuclear Lamina and is Misregulated in Emery-Dreifuss Muscular Dystrophy J Neuromuscul Dis, 2016 ; 3 (4) : 497-510
de Winter, J. M., Joureau, B., Lee, E. J., Kiss, B., Yuen, M., Gupta, V. A., Pappas, C. T., Gregorio, C. C., Stienen, G. J., Edvardson, S., Wallgren-Pettersson, C., Lehtokari, V. L., Pelin, K., Malfatti, E., Romero, N. B., Engelen, B. G., Voermans, N. C., Donkervoort, S., Bonnemann, C. G., Clarke, N. F., Beggs, A. H., Granzier, H., Ottenheijm, C. A. :
Mutation-specific effects on thin filament length in thin filament myopathy Ann Neurol, 2016 ; 79 (6) : 959-69
Mutation-specific effects on thin filament length in thin filament myopathy Ann Neurol, 2016 ; 79 (6) : 959-69
Maggio, I., Stefanucci, L., Janssen, J. M., Liu, J., Chen, X., Mouly, V., Goncalves, M. A. :
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations Nucleic Acids Res, 2016 ; 44 (3) : 1449-70
Selection-free gene repair after adenoviral vector transduction of designer nucleases: rescue of dystrophin synthesis in DMD muscle cell populations Nucleic Acids Res, 2016 ; 44 (3) : 1449-70
Roy, P., Rau, F., Ochala, J., Messeant, J., Fraysse, B., Laine, J., Agbulut, O., Butler-Browne, G., Furling, D., Ferry, A. :
Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle Skelet Muscle, 2016 ; 6 (23) : 1-17
Dystrophin restoration therapy improves both the reduced excitability and the force drop induced by lengthening contractions in dystrophic mdx skeletal muscle Skelet Muscle, 2016 ; 6 (23) : 1-17
Stojkovic, T. :
Hereditary neuropathies: An update Rev Neurol (Paris), 2016 ; 172 (12) : 775-778
Hereditary neuropathies: An update Rev Neurol (Paris), 2016 ; 172 (12) : 775-778
El Mendili, M. M., Lenglet, T., Stojkovic, T., Behin, A., Guimaraes-Costa, R., Salachas, F., Meininger, V., Bruneteau, G., Le Forestier, N., Laforet, P., Lehericy, S., Benali, H., Pradat, P. F. :
Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA PLoS ONE, 2016 ; 11 (4) : e0152439
Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA PLoS ONE, 2016 ; 11 (4) : e0152439
