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
Publications (1184)
D'Alessandro, M., Hnia, K., Gache, V., Koch, C., Gavriilidis, C., Rodriguez, D., Nicot, A. S., Romero, N. B., Schwab, Y., Gomes, E., Labouesse, M., Laporte, J. :
Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton Dev Cell, 2015 ; 35 (2) : 186-98
Amphiphysin 2 Orchestrates Nucleus Positioning and Shape by Linking the Nuclear Envelope to the Actin and Microtubule Cytoskeleton Dev Cell, 2015 ; 35 (2) : 186-98
Hewson, D. J., Duchene, J., Hogrel, J. Y. :
Validation of balance-quality assessment using a modified bathroom scale Physiol Meas, 2015 ; 36 (2) : 207-18
Validation of balance-quality assessment using a modified bathroom scale Physiol Meas, 2015 ; 36 (2) : 207-18
Zalc, A., Rattenbach, R., Aurade, F., Cadot, B., Relaix, F. :
Pax3 and Pax7 Play Essential Safeguard Functions against Environmental Stress-Induced Birth Defects Dev Cell, 2015 ; 33 (1) : 56-66
Pax3 and Pax7 Play Essential Safeguard Functions against Environmental Stress-Induced Birth Defects Dev Cell, 2015 ; 33 (1) : 56-66
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
Rocheteau, P., Chatre, L., Briand, D., Mebarki, M., Jouvion, G., Bardon, J., Crochemore, C., Serrani, P., Lecci, P. P., Latil, M., Matot, B., Carlier, P. G., Latronico, N., Huchet, C., Lafoux, A., Sharshar, T., Ricchetti, M., Chretien, F. :
Sepsis induces long-term metabolic and mitochondrial muscle stem cell dysfunction amenable by mesenchymal stem cell therapy Nat Commun, 2015 ; 6 : 10145
Sepsis induces long-term metabolic and mitochondrial muscle stem cell dysfunction amenable by mesenchymal stem cell therapy Nat Commun, 2015 ; 6 : 10145
Baudin, P. Y., Marty, B., Robert, B., Shukelovitch, A., Carlier, R. Y., Azzabou, N., Carlier, P. G. :
Qualitative and quantitative evaluation of skeletal muscle fatty degenerative changes using whole-body Dixon nuclear magnetic resonance imaging for an important reduction of the acquisition time Neuromuscul Disord, 2015 ; 25 (10) : 758-63
Qualitative and quantitative evaluation of skeletal muscle fatty degenerative changes using whole-body Dixon nuclear magnetic resonance imaging for an important reduction of the acquisition time Neuromuscul Disord, 2015 ; 25 (10) : 758-63
Azzabou, N., Loureiro de Sousa, P., Caldas, E., Carlier, P. G. :
Validation of a generic approach to muscle water T2 determination at 3T in fat-infiltrated skeletal muscle J Magn Reson Imaging, 2015 ; 2015 Mar;41(3):645-53 (3) : 645-53
Validation of a generic approach to muscle water T2 determination at 3T in fat-infiltrated skeletal muscle J Magn Reson Imaging, 2015 ; 2015 Mar;41(3):645-53 (3) : 645-53
Miro, J., Laaref, A. M., Rofidal, V., Lagrafeuille, R., Hem, S., Thorel, D., Mechin, D., Mamchaoui, K., Mouly, V., Claustres, M., Tuffery-Giraud, S. :
FUBP1: a new protagonist in splicing regulation of the DMD gene Nucleic Acids Res, 2015 ; 43 (4) : 2378-2389
FUBP1: a new protagonist in splicing regulation of the DMD gene Nucleic Acids Res, 2015 ; 43 (4) : 2378-2389
Bordet, C., Schaerer, E., Clément, S., Gargiulo, M., Durr, A. :
Passerelles: Prescription des tests génétiques : ce qui a changé Pratique Neurologique - FMC, 2015 ; 6 (1) : 49-53
Passerelles: Prescription des tests génétiques : ce qui a changé Pratique Neurologique - FMC, 2015 ; 6 (1) : 49-53
