Publications (1181)

Lecourt, S., Marolleau, J. P., Fromigue, O., Vauchez, K., Andriamanalijaona, R., Ternaux, B., Lacassagne, M. N., Robert, I., Boumediene, K., Chereau, F., Marie, P., Larghero, J., Fiszman, M., Vilquin, J. T. :
Characterization of distinct mesenchymal-like cell populations from human skeletal muscle in situ and in vitro Exp Cell Res, 2010 ; 316 (15) : 2513-2526

Uro-Coste, E, Fernandez, C, Authier, F J, Bassez, G, Butori, C, Chapon, F, Delisle, M B, Dubourg, O, Feasson, L, Gherardi, R, Lacroix, C, Laquerriere, A, Letournel, F, Magy, L, Maisonobe, T, Marcorelles, P, Maurage, C A, Mezin, P, Mussini, J M, Penisson-Besnier, I, Romero, N B, Streichenberger, N, Vallat, J M, Viennet, G, Vital, A, Voit, T, Boucharef, W, Figarella-Branger, D :
Prise en charge des biopsies musculaires et nerveuses. Recommandations formalisées d’experts sous l’égide de la Société française de neuropathologie, de la Société française de myologie et de l’Association française contre les myopathies Rev Neurol (Paris), 2010 ; 166 (5) : 477-485

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

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

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

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

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

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

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

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