Hayashi, Shinichiro, Drayton, Bernadette, Aurade, Frédéric, Rocancourt, Didier, Buckingham, Margaret, Relaix, Frédéric :
Conserved functions of Pax3/7 during evolution
Developmental Biology, 2010 ; 344 (1) : 528-529
Publications (1181)
Pinto Mariz, F, Carvalho, L. R., De Mello, W., De Queiroz Campos Araujo, A, Ribeiro, M. G., Do Carmo Soares Alves Cunha, M, Voit , T, Butler Browne, G., Dayse Silva Barbosa, S :
Differential integrin expression by T lymphocytes: potential role in DMD muscle damage J Neuroimmunol, 2010 ; 223 (1-2) : 128-130
Differential integrin expression by T lymphocytes: potential role in DMD muscle damage J Neuroimmunol, 2010 ; 223 (1-2) : 128-130
Claeys, K. G., Pellissier, J. F., Garcia-Bragado, F., Weis, J., Urtizberea, A., Poza, J. J., Cobo, A. M., Stoltenburg, G., Figarella-Branger, D., Willems, P. J., Depuydt, C. E., Kleiner, W., Pouget, J., Piraud, M., Brochier, G., Romero, N. B., Fardeau, M., Goebel, H. H., Bonnemann, C. G., Voit, T., Eymard, B., Laforet, P. :
Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity Neuromuscul Disord, 2010 ; 20 (11) : 701-708
Myopathy with hexagonally cross-linked crystalloid inclusions: Delineation of a clinico-pathological entity Neuromuscul Disord, 2010 ; 20 (11) : 701-708
Le Panse, R., Bismuth, J., Cizeron-Clairac, G., Weiss, J. M., Cufi, P., Dartevelle, P., De Rosbo, N. K., Berrih-Aknin, S. :
Thymic remodeling associated with hyperplasia in myasthenia gravis Autoimmunity, 2010 ; 43 (5-6) : 401-12
Thymic remodeling associated with hyperplasia in myasthenia gravis Autoimmunity, 2010 ; 43 (5-6) : 401-12
Trollet, C., Anvar, S. Y., Venema, A., Hargreaves, I. P., Foster, K., Vignaud, A., Ferry, A., Negroni, E., Hourde, C., Baraibar, M. A., t Hoen, P. A., Davies, J. E., Rubinsztein, D. C., Heales, S. J., Mouly, V., Raz, V., Butler-Browne, G., van der Maarel, S. M., Dickson, G. :
Molecular and phenotypic characterisation of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres Hum Mol Genet, 2010 ; 19 (11) : 2191-21207
Molecular and phenotypic characterisation of a mouse model of oculopharyngeal muscular dystrophy reveals severe muscular atrophy restricted to fast glycolytic fibres Hum Mol Genet, 2010 ; 19 (11) : 2191-21207
Arzel-Hezode, M., Sternberg, D., Tabti, N., Vicart, S., Goizet, C., Eymard, B., Fontaine, B., Fournier, E. :
Homozygosity for dominant mutations increases severity of muscle channelopathies Muscle Nerve, 2010 ; 41 (4) : 470-7
Homozygosity for dominant mutations increases severity of muscle channelopathies Muscle Nerve, 2010 ; 41 (4) : 470-7
Finsterer, J., Ramaciotti, C., Wang, C. H., Wahbi, K., Rosenthal, D., Duboc, D., Melacini, P. :
Cardiac Findings in Congenital Muscular Dystrophies Pediatrics, 2010 ; 126 (3) : 538-545
Cardiac Findings in Congenital Muscular Dystrophies Pediatrics, 2010 ; 126 (3) : 538-545
Mitchell, K. J., Pannerec, A., Cadot, B., Parlakian, A., Besson, V., Gomes, E. R., Marazzi, G., Sassoon, D. A. :
Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development Nat Cell Biol, 2010 ; 12 (3) : 257-66
Identification and characterization of a non-satellite cell muscle resident progenitor during postnatal development Nat Cell Biol, 2010 ; 12 (3) : 257-66
Wang, C. H., Bonnemann, C. G., Rutkowski, A., Sejersen, T., Bellini, J., Battista, V., Florence, J. M., Schara, U., Schuler, P. M., Wahbi, K., Aloysius, A., Bash, R. O., Beroud, C., Bertini, E., Bushby, K., Cohn, R. D., Connolly, A. M., Deconinck, N., Desguerre, I., Eagle, M., Estournet-Mathiaud, B., Ferreiro, A., Fujak, A., Goemans, N., Iannaccone, S. T., Jouinot, P., Main, M., Melacini, P., Mueller-Felber, W., Muntoni, F., Nelson, L. L., Rahbek, J., Quijano-Roy, S., Sewry, C., Storhaug, K., Simonds, A., Tseng, B., Vajsar, J., Vianello, A., Zeller, R. :
Consensus Statement on Standard of Care for Congenital Muscular Dystrophies J Child Neurol, 2010 ; 25 (12) : 1559-1581
Consensus Statement on Standard of Care for Congenital Muscular Dystrophies J Child Neurol, 2010 ; 25 (12) : 1559-1581
Benson, E. K., Zhao, B., Sassoon, D. A., Lee, S. W., Aaronson, S. A. :
Effects of p21 deletion in mouse models of premature aging Cell Cycle, 2009 ; 8 (13) : 2002-4
Effects of p21 deletion in mouse models of premature aging Cell Cycle, 2009 ; 8 (13) : 2002-4
