Benveniste, O., Leger, J. M. :
Inflammatory or necrotizing myopathies, myositides and other acquired myopathies, new insight in 2011
Presse Med, 2011 ; 40 (4 Pt 2) : e197-8
Publications (1184)
Hanisch, F., Muller, T., Dietz, A., Bitoun, M., Kress, W., Weis, J., Stoltenburg, G., Zierz, S. :
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations J Neurol, 2011 ; 258 (6) : 1085-90
Phenotype variability and histopathological findings in centronuclear myopathy due to DNM2 mutations J Neurol, 2011 ; 258 (6) : 1085-90
Meune, C., Wahbi, K., Weber, S., Zuily, S., Cynober, L., Chenevier-Gobeaux, C. :
Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome Clin Biochem, 2011 ; 44 (16) : 1343-1345
Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome Clin Biochem, 2011 ; 44 (16) : 1343-1345
Castets, P., Bertrand, A. T., Beuvin, M., Ferry, A., Le Grand, F., Castets, M., Chazot, G., Rederstorff, M., Krol, A., Lescure, A., Romero, N. B., Guicheney, P., Allamand, V. :
Satellite cell loss and impaired muscle regeneration in Selenoprotein N deficiency Hum Mol Genet, 2011 ; 20 (4) : 694-704
Satellite cell loss and impaired muscle regeneration in Selenoprotein N deficiency Hum Mol Genet, 2011 ; 20 (4) : 694-704
Klein, A. F., Gasnier, E., Furling, D. :
Gain of RNA function in pathological cases: Focus on myotonic dystrophy Biochimie, 2011 ; 93 (11) : 2006-12
Gain of RNA function in pathological cases: Focus on myotonic dystrophy Biochimie, 2011 ; 93 (11) : 2006-12
Redondo-Verge, L., Benyaou, R., Fernandez-Recio, M., Dinca, L., Richard, P., Bonne, G. :
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophy Muscle Nerve, 2011 ; 44 (4) : 587-9
Cardioembolic stroke prompting diagnosis of LMNA-associated Emery-Dreifuss muscular dystrophy Muscle Nerve, 2011 ; 44 (4) : 587-9
Thibaud, J. L., Wary, C, Barthélémy, I, Blot, S, Carlier, P. G. :
Évaluation par résonance magnétique nucléaire du muscle strié squelettique et cardiaque du chien déficient en dystrophine Pratique Médicale et Chirurgicale de l'Animal de Compagnie, 2011 ; 46 (3) : 83-90
Évaluation par résonance magnétique nucléaire du muscle strié squelettique et cardiaque du chien déficient en dystrophine Pratique Médicale et Chirurgicale de l'Animal de Compagnie, 2011 ; 46 (3) : 83-90
Angeard, N., Jacquette, A., Gargiulo, M., Radvanyi, H., Moutier, S., Eymard, B., Heron, D. :
A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1) Neuromuscul Disord, 2011 ; 21 (7) : 468-476
A new window on neurocognitive dysfunction in the childhood form of myotonic dystrophy type 1 (DM1) Neuromuscul Disord, 2011 ; 21 (7) : 468-476
Duijnisveld, B. J., Bigot, A., Beenakker, K. G., Portilho, D., Raz, V., van der Heide, H. J., Visser, C. P., Chaouch, S., Mamchaoui, K., Westendorp, R. G., Mouly, V., Butler-Browne, G. S., Nelissen, R. G., Maier, A. B. :
Regenerative potential of human muscle stem cells in chronic inflammation Arthritis Res Ther, 2011 ; 13 (6) : R207
Regenerative potential of human muscle stem cells in chronic inflammation Arthritis Res Ther, 2011 ; 13 (6) : R207
Lu, Q. L., Yokota, T., Takeda, S., Garcia, L., Muntoni, F., Partridge, T. :
The Status of Exon Skipping as a Therapeutic Approach to Duchenne Muscular Dystrophy Mol Ther, 2011 ; 19 (1) : 9-15
The Status of Exon Skipping as a Therapeutic Approach to Duchenne Muscular Dystrophy Mol Ther, 2011 ; 19 (1) : 9-15
