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
Publications (1181)
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
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
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
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
Human galectin 3 binding protein interacts with recombinant adeno-associated virus type 6 J Virol, 2012 ; 86 (12) : 6620-6631
Hoogaars, W., Mouisel, E., Pasternack, A., Hulmi, J. J., Relizani, K., Schuelke, M., Schirwis, E., Garcia, L., Ritvos, O., Ferry, A., t Hoen, P. A., Amthor, H. :
Combined effect of AAV-U7-induced dystrophin exon skipping and soluble activin type IIB receptor in mdx mice Hum Gene Ther, 2012 ; 23 (12) : 1269-79
Combined effect of AAV-U7-induced dystrophin exon skipping and soluble activin type IIB receptor in mdx mice Hum Gene Ther, 2012 ; 23 (12) : 1269-79
Preisler, N., Laforet, P., Madsen, K. L., Hansen, R. S., Lukacs, Z., Orngreen, M. C., Lacour, A., Vissing, J. :
Fat and carbohydrate metabolism during exercise in late-onset Pompe disease Mol Genet Metab, 2012 ; 107 (3) : 462-468
Fat and carbohydrate metabolism during exercise in late-onset Pompe disease Mol Genet Metab, 2012 ; 107 (3) : 462-468
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
ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome Nat Genet, 2012 ; 44 (5) : 575-580
BĂ©hin, A, LĂ©ger, J M :
Quand recourir Ă la Commission permanente des permis de conduire ? Neurologie Pratique, 2012 ; 80 : 9-10
Quand recourir Ă la Commission permanente des permis de conduire ? Neurologie Pratique, 2012 ; 80 : 9-10
Fraysse, B, Weinberger, F, Bardswell, S, Cuello, F, Vignier, N, Geertz, B, Starbatty, J, KrÀmer, E, Coirault, C, Eschenhagen, T, Kentish, J C, Avkiran, M, Carrier, L :
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice J Mol Cell Cardiol, 2012 ; 52 : 1299-1307
Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice J Mol Cell Cardiol, 2012 ; 52 : 1299-1307
Ledoux, I., Laforet, P., Wary, C., Carlier, P. G., Hogrel, J. Y. :
Explorations de lâintolĂ©rance musculaire Ă lâeffort de lâenfant Arch Pediatr, 2012 ; 19 (6 S1) : H107-H108
Explorations de lâintolĂ©rance musculaire Ă lâeffort de lâenfant Arch Pediatr, 2012 ; 19 (6 S1) : H107-H108
