Romero, N. B., Bitoun, M. :
Centronuclear myopathies
Semin Pediatr Neurol, 2011 ; 18 (4) : 250-6
Publications (1184)
Baraibar, M. A., Hyzewicz, J., Rogowska-Wresinska, A., Ladouce, R., Roepstorff, P., Mouly, V., Friguet, B. :
Oxidative stress-induced proteome alterations target different cellular pathways in human myoblasts Free Radic Biol Med, 2011 ; 51 (8) : 1522-1532
Oxidative stress-induced proteome alterations target different cellular pathways in human myoblasts Free Radic Biol Med, 2011 ; 51 (8) : 1522-1532
Forsha, D., Li, J. S., Smith, P. B., van der Ploeg, A. T., Kishnani, P., Pasquali, S. K., Laforet, P :
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy Genet Med, 2011 ; 13 (7) : 625-631
Cardiovascular abnormalities in late-onset Pompe disease and response to enzyme replacement therapy Genet Med, 2011 ; 13 (7) : 625-631
Mayeuf, A., Relaix, F. :
La voie Notch – Du developpement a la regeneration du muscle squelettique. Med Sci (Paris), 2011 ; 27 (5) : 521-526
La voie Notch – Du developpement a la regeneration du muscle squelettique. Med Sci (Paris), 2011 ; 27 (5) : 521-526
Vieitez, I., Teijeira, S., Fernandez, J. M., San Millan, B., Miranda, S., Ortolano, S., Louis, S., Laforet, P., Navarro, C. :
Molecular and clinical study of McArdle’s disease in a cohort of 123 European patients. Identification of 20 novel mutations Neuromuscul Disord, 2011 ; 21 (12) : 817-823
Molecular and clinical study of McArdle’s disease in a cohort of 123 European patients. Identification of 20 novel mutations Neuromuscul Disord, 2011 ; 21 (12) : 817-823
Besson, V., Smeriglio, P., Wegener, A., Relaix, F., Oumesmar, B. N., Sassoon, D. A., Marazzi, G. :
PW1 gene/paternally expressed gene 3 (PW1/Peg3) identifies multiple adult stem and progenitor cell populations Proc Natl Acad Sci U S A, 2011 ; 108 (28) : 11470-5
PW1 gene/paternally expressed gene 3 (PW1/Peg3) identifies multiple adult stem and progenitor cell populations Proc Natl Acad Sci U S A, 2011 ; 108 (28) : 11470-5
Hervier, B., Uzunhan, Y., Hachulla, E., Benveniste, O., Nunes, H., Delaval, P., Musset, L., Dubucquoi, S., Wallaert, B., Hamidou, M. :
Antisynthetase syndrome positive for anti-threonyl-tRNA synthetase (anti-PL7) antibodies Eur Respir J, 2011 ; 37 (3) : 714-717
Antisynthetase syndrome positive for anti-threonyl-tRNA synthetase (anti-PL7) antibodies Eur Respir J, 2011 ; 37 (3) : 714-717
Negroni, E., Vallese, D., Vilquin, J. T., Butler-Browne, G., Mouly, V., Trollet, C. :
Current advances in cell therapy strategies for muscular dystrophies Expert Opin Biol Ther, 2011 ; 11 (2) : 157-176
Current advances in cell therapy strategies for muscular dystrophies Expert Opin Biol Ther, 2011 ; 11 (2) : 157-176
Cifuentes-Diaz, C., Dubourg, O., Irinopoulou, T., Vigny, M., Lachkar, S., Decker, L., Charnay, P., Denisenko, N., Maisonobe, T., Leger, J. M., Viala, K., Hauw, J. J., Girault, J. A. :
Nodes of ranvier and paranodes in chronic acquired neuropathies PLoS ONE, 2011 ; 6 (1) : e14533
Nodes of ranvier and paranodes in chronic acquired neuropathies PLoS ONE, 2011 ; 6 (1) : e14533
Laloui, K., Wary, C., Carlier, R. Y., Hogrel, J. Y., Caillaud, C., Laforet, P. :
Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat ? Neurology, 2011 ; 77 (6) : 594-5
Making diagnosis of Pompe disease at a presymptomatic stage: To treat or not to treat ? Neurology, 2011 ; 77 (6) : 594-5
