Yuen, M., Sandaradura, S. A., Dowling, J. J., Kostyukova, A. S., Moroz, N., Quinlan, K. G., Lehtokari, V. L., Ravenscroft, G., Todd, E. J., Ceyhan-Birsoy, O., Gokhin, D. S., Maluenda, J., Lek, M., Nolent, F., Pappas, C. T., Novak, S. M., D'Amico, A., Malfatti, E., Thomas, B. P., Gabriel, S. B., Gupta, N., Daly, M. J., Ilkovski, B., Houweling, P. J., Davidson, A. E., Swanson, L. C., Brownstein, C. A., Gupta, V. A., Medne, L., Shannon, P., Martin, N., Bick, D. P., Flisberg, A., Holmberg, E., Van den Bergh, P., Lapunzina, P., Waddell, L. B., Sloboda, D. D., Bertini, E., Chitayat, D., Telfer, W. R., Laquerriere, A., Gregorio, C. C., Ottenheijm, C. A., Bonnemann, C. G., Pelin, K., Beggs, A. H., Hayashi, Y. K., Romero, N. B., Laing, N. G., Nishino, I., Wallgren-Pettersson, C., Melki, J., Fowler, V. M., MacArthur, D. G., North, K. N., Clarke, N. F. :
Leiomodin-3 dysfunction results in thin filament disorganization and nemaline myopathy – Erratum
J Clin Invest, 2015 ; 125 (1) : 456-7
Publications (1181)
Santos, D. B., Boussaid, G., Stojkovic, T., Orlikowski, D., Letilly, N., Behin, A., Butel, S., Lofaso, F., Prigent, H. :
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy Neuromuscul Disord, 2015 ; 25 (8) : 632-9
Respiratory muscle dysfunction in facioscapulohumeral muscular dystrophy Neuromuscul Disord, 2015 ; 25 (8) : 632-9
Negroni, E., Bigot, A., Butler-Browne, G., Trollet, C., Mouly, V. :
Cellular therapies for muscular dystrophies: frustrations and clinical successes Hum Gene Ther, 2015 ; :
Cellular therapies for muscular dystrophies: frustrations and clinical successes Hum Gene Ther, 2015 ; :
Henique, C., Mansouri, A., Vavrova, E., Lenoir, V., Ferry, A., Esnous, C., Ramond, E., Girard, J., Bouillaud, F., Prip-Buus, C., Cohen, I. :
Increasing mitochondrial muscle fatty acid oxidation induces skeletal muscle remodeling toward an oxidative phenotype FASEB J, 2015 ; 29 (6) : 2473-83
Increasing mitochondrial muscle fatty acid oxidation induces skeletal muscle remodeling toward an oxidative phenotype FASEB J, 2015 ; 29 (6) : 2473-83
Mariani, L. L., Lozeron, P., Theaudin, M., Mincheva, Z., Signate, A., Ducot, B., Algalarrondo, V., Denier, C., Adam, C., Nicolas, G., Samuel, D., Slama, M. S., Lacroix, C., Misrahi, M., Adams, D., Maisonobe, T, Léger, J M, Stojkovic, T, Viala, K, Lenglet, T, Antoine, J C, Camdessanche, J P, Vial, C, Petiot, P, Magy, L, Vallat, J M, Pouget, J, Attarian, S, Franques, J, Desnuelle, C, Delmont, E, Lacour, A, Hachulla, E, le Masson, G, Sole, G, Pereon, Y, Echaniz-Laguna, A, Tranchant, C, Labauge, P, Morales, R J, Corcia, P, Bellance, R, Mignard, C, Clavelou, P, Guiraud-Chaumeil, C, Guegen, A. :
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France Ann Neurol, 2015 ; 78 (6) : 901-16
Genotype-phenotype correlation and course of transthyretin familial amyloid polyneuropathies in France Ann Neurol, 2015 ; 78 (6) : 901-16
Allenbach, Y, Leroux, G, Preusse, C, Suarez Calvet, X, Gallardo, E, Hervier, B, Rigolet, A, Hie, M, Limal, N, Hufnagl, P, Zerbe, N, Meyer, A, Maisonobe, T, Aouizerate, J, Uzunhan, Y, Goebel, H H, Benveniste, O, Stenzel, W :
Dermatomyositis with or without anti-MDA5 antibodies: common Interferon signature but distinct NOS2 expression Acta Neuropathol Commun, 2015 ; (SP) :
Dermatomyositis with or without anti-MDA5 antibodies: common Interferon signature but distinct NOS2 expression Acta Neuropathol Commun, 2015 ; (SP) :
Michon, C. C., Gargiulo, M., Hahn-Barma, V., Petit, F., Nadaj-Pakleza, A., Herson, A., Eymard, B., Labrune, P., Laforet, P. :
Cognitive profile of patients with glycogen storage disease type III: a clinical description of seven cases J Inherit Metab Dis, 2015 ; 38 (3) : 573-580
Cognitive profile of patients with glycogen storage disease type III: a clinical description of seven cases J Inherit Metab Dis, 2015 ; 38 (3) : 573-580
Clément, S., Gargiulo, M., Feingold, J., Durr, A. :
Lignes directrices et bonnes pratiques du test présymptomatique de la maladie de Huntington : passé, présent et futur en France Revue neurologique, 2015 ; 171 (6-7) : 572-580
Lignes directrices et bonnes pratiques du test présymptomatique de la maladie de Huntington : passé, présent et futur en France Revue neurologique, 2015 ; 171 (6-7) : 572-580
Latroche, C., Matot, B., Martins-Bach, A., Briand, D., Chazaud, B., Wary, C., Carlier, P. G., Chretien, F., Jouvion, G. :
Structural and Functional Alterations of Skeletal Muscle Microvasculature in Dystrophin-Deficient mdx Mice Am J Pathol, 2015 ; 185 (9) : 2482-94
Structural and Functional Alterations of Skeletal Muscle Microvasculature in Dystrophin-Deficient mdx Mice Am J Pathol, 2015 ; 185 (9) : 2482-94
Toussaint, M., Gilles, R. J., Azzabou, N., Marty, B., Vignaud, A., Greiser, A., Carlier, P. G. :
Characterization of Benign Myocarditis Using Quantitative Delayed-Enhancement Imaging Based on Molli T1 Mapping Medicine (Baltimore), 2015 ; 94 (43) : e1868
Characterization of Benign Myocarditis Using Quantitative Delayed-Enhancement Imaging Based on Molli T1 Mapping Medicine (Baltimore), 2015 ; 94 (43) : e1868
