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
Publications (1181)
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, LĂ©ger, 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
Boisgerault, F., Mingozzi, F. :
The Skeletal Muscle Environment and Its Role in Immunity and Tolerance to AAV Vector-Mediated Gene Transfer Curr Gene Ther, 2015 ; 15 (4) : 381-94
The Skeletal Muscle Environment and Its Role in Immunity and Tolerance to AAV Vector-Mediated Gene Transfer Curr Gene Ther, 2015 ; 15 (4) : 381-94
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
Crudele, J. M., Finn, J. D., Siner, J. I., Martin, N. B., Niemeyer, G. P., Zhou, S., Mingozzi, F., Lothrop, C. D., Jr., Arruda, V. R. :
AAV liver expression of FIX-Padua prevents and eradicates FIX inhibitor without increasing thrombogenicity in hemophilia B dogs and mice Blood, 2015 ; 125 (10) : 1553-1561
AAV liver expression of FIX-Padua prevents and eradicates FIX inhibitor without increasing thrombogenicity in hemophilia B dogs and mice Blood, 2015 ; 125 (10) : 1553-1561
Rau, F, Lainé, J, Ramanoudjame, L, Ferry, A, Arandel, L, Delalande, O, Jollet, A, Dingli, F, Lee, K Y, Peccate, C, Lorain, S, Kabashi, E, Athansopoulos, T, Koo, T, Loew, D, Swanson, M, Le Rumeur, E, Dickson, G, Allamand, V, Marie, J, Furling, D :
Abnormal splicing switch of DMD’s penultimate exon compromises muscle fiber maintenance in Myotonic Dystrophy Nat Commun, 2015 ; 6 : 7205
Abnormal splicing switch of DMD’s penultimate exon compromises muscle fiber maintenance in Myotonic Dystrophy Nat Commun, 2015 ; 6 : 7205
Meyer, A., Lefevre, G., Bierry, G., Duval, A., Ottaviani, S., Meyer, O., Tournadre, A., Le Goff, B., Messer, L., Buchdahl, A. L., De Bandt, M., Deligny, C., Dubois, M., Coquerelle, P., Falgarone, G., Flipo, R. M., Mathian, A., Geny, B., Amoura, Z., Benveniste, O., Hachulla, E., Sibilia, J., Hervier, B. :
In antisynthetase syndrome, ACPA are associated with severe and erosive arthritis: an overlapping rheumatoid arthritis and antisynthetase syndrome Medicine (Baltimore), 2015 ; 94 (20) : e523
In antisynthetase syndrome, ACPA are associated with severe and erosive arthritis: an overlapping rheumatoid arthritis and antisynthetase syndrome Medicine (Baltimore), 2015 ; 94 (20) : e523
