Hogrel, J. Y. :
DM1 et essais thĂ©rapeutiques : critĂšres neuromusculaires d’Ă©valuation
Cahier de Myologie, 2011 ; 5 : 11-14
Publications (1181)
Orlikowski, D., Pellegrini, N., Prigent, H., Laforet, P., Carlier, R., Carlier, P. G., Eymard, B., Lofaso, F., Annane, D. :
Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease Neuromuscul Disord, 2011 ; 21 (7) : 477-482
Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease Neuromuscul Disord, 2011 ; 21 (7) : 477-482
Bachmeyer, C., Ferroir, J. P., Eymard, B., Maier-Redelsperger, M., Lebre, A. S., Girot, R. :
Coenzyme Q is effective on anemia in a patient with sideroblastic anemia and mitochondrial myopathy Blood, 2010 ; 116 (18) : 3681-2
Coenzyme Q is effective on anemia in a patient with sideroblastic anemia and mitochondrial myopathy Blood, 2010 ; 116 (18) : 3681-2
Fraysse, B., Nagi, S. M., Boher, B., Ragot, H., Laine, J., Salmon, A., Fiszman, M. Y., Toussaint, M., Fromes, Y. :
Ca2+ overload and mitochondrial permeability transition pore activation in living {delta}-sarcoglycan deficient cardiomyocytes Am J Physiol Cell Physiol, 2010 ; 299 (3) : C706-13
Ca2+ overload and mitochondrial permeability transition pore activation in living {delta}-sarcoglycan deficient cardiomyocytes Am J Physiol Cell Physiol, 2010 ; 299 (3) : C706-13
Mizrachi, K., Aricha, R., Feferman, T., Kela-Madar, N., Mandel, I., Paperna, T., Miller, A., Ben-Nun, A., Berrih-Aknin, S., Souroujon, M. C., Fuchs, S. :
Involvement of phosphodiesterases in autoimmune diseases J Neuroimmunol, 2010 ; 220 (1-2) : 43-51
Involvement of phosphodiesterases in autoimmune diseases J Neuroimmunol, 2010 ; 220 (1-2) : 43-51
Wary, C., Nadaj-Pakleza, A., Laforet, P., Claeys, K. G., Carlier, R., Monnet, A., Fleury, S., Baligand, C., Eymard, B., Labrune, P., Carlier, P. G. :
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy Neuromuscul Disord, 2010 ; 20 (8) : 548-558
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopy Neuromuscul Disord, 2010 ; 20 (8) : 548-558
Scelles, R, Aubert-Godard, A, Gargiulo, M, Avant, M, Gortais, J :
Revealing a child’s pathology : physicians’ experiences Early Child Development and Care, 2010 ; 180 (6) : 743-752
Revealing a child’s pathology : physicians’ experiences Early Child Development and Care, 2010 ; 180 (6) : 743-752
Brinas, L., Richard, P., Quijano-Roy, S., Gartioux, C., Ledeuil, C., Lacene, E., Makri, S., Ferreiro, A., Maugenre, S., Topaloglu, H., Haliloglu, G., Penisson-Besnier, I., Jeannet, P. Y., Merlini, L., Navarro, C., Toutain, A., Chaigne, D., Desguerre, I., de Die-Smulders, C., Dunand, M., Echenne, B., Eymard, B., Kuntzer, T., Maincent, K., Mayer, M., Plessis, G., Rivier, F., Roelens, F., Stojkovic, T., Lia Taratuto, A., Lubieniecki, F., Monges, S., Tranchant, C., Viollet, L., Romero, N. B., Estournet, B., Guicheney, P., Allamand, V. :
Early onset collagen VI myopathies: Genetic and clinical correlations Ann Neurol, 2010 ; 68 (4) : 511-520
Early onset collagen VI myopathies: Genetic and clinical correlations Ann Neurol, 2010 ; 68 (4) : 511-520
Izmiryan, A., Peltekian, E., Paulin, D., Li, Z., Xue, Z. :
Synemin Isoforms in Astroglial and Neuronal Cells from Human Central Nervous System Neurochem Res, 2010 ; 35 (6) : 881-887
Synemin Isoforms in Astroglial and Neuronal Cells from Human Central Nervous System Neurochem Res, 2010 ; 35 (6) : 881-887
Randles, K. N., Lam, L. T., Sewry, C. A., Puckelwartz, M., Furling, D., Wehnert, M., McNally, E. M., Morris, G. E. :
Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle development Dev Dyn, 2010 ; 239 (3) : 998-1009
Nesprins, but not sun proteins, switch isoforms at the nuclear envelope during muscle development Dev Dyn, 2010 ; 239 (3) : 998-1009