Publications (1181)

Faure, C., Raynaud-Simon, A., Ferry, A., Dauge, V., Cynober, L., Aussel, C., Moinard, C. :
Leucine and citrulline modulate muscle function in malnourished aged rats Amino Acids, 2012 ; 42 (4) : 1425-1433
Lebeaux, D., Frances, C., Barete, S., Wechsler, B., Dubourg, O., Renoux, J., Maisonobe, T., Benveniste, O., Gatfosse, M., Bourgeois, P., Amoura, Z., Cacoub, P., Piette, J. C., Sene, D. :
Eosinophilic fasciitis (Shulman disease): new insights into the therapeutic management from a series of 34 patients Rheumatology (Oxford), 2012 ; 51 (3) : 557-561
Vuillerot, C., Payan, C., Girardot, F., Fermanian, J., Iwaz, J., Berard, C., Ecochard, R. :
Responsiveness of the Motor Function Measure in neuromuscular diseases Arch Phys Med Rehabil, 2012 ; 93 (12) : 2251-6
Chaumeil, M. M., Valette, J., Baligand, C., Brouillet, E., Hantraye, P., Bloch, G., Gaura, V., Rialland, A., Krystkowiak, P., Verny, C., Damier, P., Remy, P., Bachoud-Levi, A. C., Carlier, P. G., Lebon, V. :
pH as a biomarker of neurodegeneration in Huntington’s disease: a translational rodent-human MRS study J Cereb Blood Flow Metab, 2012 ; 32 (5) : 771-9
Boërio, D., Lefaucheur, J. P., Bassez, G., Hogrel, J. Y. :
Central and peripheral components of exercise-related fatigability in myotonic dystrophy type 1 Acta Neurol Scand, 2012 ; 125 (1) : 38-46
Gradolatto, A., Nazzal, D., Foti, M., Bismuth, J., Truffault, F., Panse, R. L., Berrih-Aknin, S. :
Defects of immunoregulatory mechanisms in myasthenia gravis: role of IL-17 Ann N Y Acad Sci, 2012 ; 1274 (1) : 40-7
Meune, C., Wahbi, K., Vermillet, A., Guerin, S., Aelion, H., Weber, S., Chenevier-Gobeaux, C. :
N-Terminal-proBrain natriuretic peptide measurement at presentation to identify patients with recent onset of atrial fibrillation Int J Cardiol, 2012 ; 154 (2) : 208-209
Willer, T., Lee, H., Lommel, M., Yoshida-Moriguchi, T., de Bernabe, D. B., Venzke, D., Cirak, S., Schachter, H., Vajsar, J., Voit, T., Muntoni, F., Loder, A. S., Dobyns, W. B., Winder, T. L., Strahl, S., Mathews, K. D., Nelson, S. F., Moore, S. A., Campbell, K. P. :
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Nat Genet, 2012 ; 44 (5) : 575-580
Allenbach, Y., Benveniste, O., Decostre, V., Canal, A., Eymard, B., Herson, S., Bloch-Queyrat, C., Hogrel, J. Y. :
Quadriceps strength is a sensitive marker of disease progression in sporadic inclusion body myositis Neuromuscul Disord, 2012 ; 22 (11) : 980-986
Denard, J., Beley, C., Kotin, R., Lai-Kuen, R., Blot, S., Leh, H., Asokan, A., Samulski, R. J., Moullier, P., Voit, T., Garcia, L., Svinartchouk, F. :
Human galectin 3 binding protein interacts with recombinant adeno-associated virus type 6 J Virol, 2012 ; 86 (12) : 6620-6631