Svahn, J., Streichenberger, N., Benveniste, O., Menassa, R., Michel, L., Fayolle, H., Petiot, P. :
Significant response to immune therapies in a case of subacute necrotizing myopathy and FKRP mutations
Neuromuscul Disord, 2015 ; 25 (11) : 865-8
Publications (1184)
Decorte, N., Lamalle, L., Carlier, P. G., Giacomini, E., Guinot, M., Levy, P., Verges, S., Wuyam, B. :
Impact of salbutamol on muscle metabolism assessed by PNMR spectroscopy Scand J Med Sci Sports, 2015 ; 25 (3) : e267-73
Impact of salbutamol on muscle metabolism assessed by PNMR spectroscopy Scand J Med Sci Sports, 2015 ; 25 (3) : e267-73
Berger, A., Lorain, S., Josephine, C., Desrosiers, M., Peccate, C., Voit, T., Garcia, L., Sahel, J. A., Bemelmans, A. P. :
Repair of rhodopsin mRNA by spliceosome-mediated RNA trans-splicing: a new approach for autosomal dominant retinitis pigmentosa Mol Ther, 2015 ; 23 (5) : 918-930
Repair of rhodopsin mRNA by spliceosome-mediated RNA trans-splicing: a new approach for autosomal dominant retinitis pigmentosa Mol Ther, 2015 ; 23 (5) : 918-930
Nunes, J. C., Rinnenthal, J. L., Allenbach, Y., Lenze, D., Hummel, M., Johrens, K., Walz, R., Goebel, H. H., Heppner, F. L., Stenzel, W. :
Proximal weakness in a patient with MALT lymphoma: a case report and discussion of possible pathogenesis Neuropathol Appl Neurobiol, 2015 ; 41 (5) : 686-689
Proximal weakness in a patient with MALT lymphoma: a case report and discussion of possible pathogenesis Neuropathol Appl Neurobiol, 2015 ; 41 (5) : 686-689
Reijnierse, E. M., Trappenburg, M. C., Leter, M. J., Sipila, S., Stenroth, L., Narici, M. V., Hogrel, J. Y., Butler-Browne, G., McPhee, J. S., Paasuke, M., Gapeyeva, H., Meskers, C. G., Maier, A. B. :
Serum albumin and muscle measures in a cohort of healthy young and old participants Age (Dordr), 2015 ; 37 (5) : 88
Serum albumin and muscle measures in a cohort of healthy young and old participants Age (Dordr), 2015 ; 37 (5) : 88
Laustriat, D., Gide, J., Barrault, L., Chautard, E., Benoit, C., Auboeuf, D., Boland, A., Battail, C., Artiguenave, F., Deleuze, J. F., Benit, P., Rustin, P., Franc, S., Charpentier, G., Furling, D., Bassez, G., Nissan, X., Martinat, C., Peschanski, M., Baghdoyan, S. :
In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin Mol Ther Nucleic Acids, 2015 ; 4 : e262
In Vitro and In Vivo Modulation of Alternative Splicing by the Biguanide Metformin Mol Ther Nucleic Acids, 2015 ; 4 : e262
Lefevre, G., Meyer, A., Launay, D., Machelart, I., DeBandt, M., Michaud, J., Tournadre, A., Godmer, P., Kahn, J. E., Behra-Marsac, A., Timsit, M. A., Schleinitz, N., Wendling, D., Melac-Ducamp, S., Boyer, P., Peretz, A., Lequerre, T., Richez, C., Stervinou-Wemeau, L., Morell-Dubois, S., Lambert, M., Dubucquoi, S., Wallaert, B., Benveniste, O., Flipo, R. M., Hatron, P. Y., Sibilia, J., Hachulla, E., Hervier, B. :
Seronegative polyarthritis revealing antisynthetase syndrome: a multicentre study of 40 patients Rheumatology (Oxford), 2015 ; 54 (5) : 927-32
Seronegative polyarthritis revealing antisynthetase syndrome: a multicentre study of 40 patients Rheumatology (Oxford), 2015 ; 54 (5) : 927-32
Tchikviladze, M., Gilleron, M., Maisonobe, T., Galanaud, D., Laforet, P., Durr, A., Eymard, B., Mochel, F., Ogier, H., Behin, A., Stojkovic, T., Degos, B., Gourfinkel-An, I., Sedel, F., Anheim, M., Elbaz, A., Viala, K., Vidailhet, M., Brice, A., Jardel, C., Lombes, A. :
A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity J Neurol Neurosurg Psychiatry, 2015 ; 86 (6) : 646-654
A diagnostic flow chart for POLG-related diseases based on signs sensitivity and specificity J Neurol Neurosurg Psychiatry, 2015 ; 86 (6) : 646-654
Echigoya, Y., Mouly, V., Garcia, L., Yokota, T., Duddy, W. :
In silico screening based on predictive algorithms as a design tool for exon skipping oligonucleotides in duchenne muscular dystrophy PLoS ONE, 2015 ; 10 (3) : e0120058
In silico screening based on predictive algorithms as a design tool for exon skipping oligonucleotides in duchenne muscular dystrophy PLoS ONE, 2015 ; 10 (3) : e0120058
Semplicini, C., Vissing, J., Dahlqvist, J. R., Stojkovic, T., Bello, L., Witting, N., Duno, M., Leturcq, F., Bertolin, C., D'Ambrosio, P., Eymard, B., Angelini, C., Politano, L., Laforet, P., Pegoraro, E. :
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E Neurology, 2015 ; 84 (17) : 1772-1781
Clinical and genetic spectrum in limb-girdle muscular dystrophy type 2E Neurology, 2015 ; 84 (17) : 1772-1781
