Publications (1181)

Meune, C., Zuily, S., Wahbi, K., Claessens, Y. E., Weber, S., Chenevier-Gobeaux, C. :
Combination of copeptin and high-sensitivity cardiac troponin T assay in unstable angina and non-ST-segment elevation myocardial infarction: A pilot study Arch Cardiovasc Dis, 2011 ; 104 (1) : 4-10
Cavalcante, P., Le Panse, R., Berrih-Aknin, S., Maggi, L., Antozzi, C., Baggi, F., Bernasconi, P., Mantegazza, R. :
The thymus in myasthenia gravis: Site of « innate autoimmunity »? Muscle Nerve, 2011 ; 44 (4) : 467-84
Koo, T., Malerba, A., Athanasopoulos, T., Trollet, C., Boldrin, L., Ferry, A., Popplewell, L., Foster, H., Foster, K., Dickson, G. :
Delivery of AAV2/9-Microdystrophin Genes Incorporating Helix 1 of the Coiled-Coil Motif in the C-Terminal Domain of Dystrophin Improves Muscle Pathology and Restores the Level of alpha1-Syntrophin and alpha-Dystrobrevin in Skeletal Muscles of mdx Mice Hum Gene Ther, 2011 ; 22 (11) : 1379-1388
Rolland, Y., Verin, M., Payan, C. A., Duchesne, S., Kraft, E., Hauser, T. K., Jarosz, J., Deasy, N., Defevbre, L., Delmaire, C., Dormont, D., Ludolph, A. C., Bensimon, G., Leigh, P. N. :
A new MRI rating scale for progressive supranuclear palsy and multiple system atrophy: validity and reliability J Neurol Neurosurg Psychiatry, 2011 ; 82 (9) : 1025-1032
Angeard, N., Babonneau, M. L., Frischmann, M., Gallais, B., Gargiulo, M., Herson, A., Michon, C. C., RéveillÚre, C. :
Evolution des connaissances psychologiques, neuropsychologiques et des pratiques cliniques Journal de réadaptation médicale, 2011 ; 31 (3) : 178-185
Aricha, R., Feferman, T., Scott, H. S., Souroujon, M. C., Berrih-Aknin, S., Fuchs, S. :
The susceptibility of Aire(-/-) mice to experimental myasthenia gravis involves alterations in regulatory T cells J Autoimmun, 2011 ; 36 (1) : 16-24
Ellinwood, N. M., Ausseil, J., Desmaris, N., Bigou, S., Liu, S., Jens, J. K., Snella, E. M., Mohammed, E. E., Thomson, C. B., Raoul, S., Joussemet, B., Roux, F., Cherel, Y., Lajat, Y., Piraud, M., Benchaouir, R., Hermening, S., Petry, H., Froissart, R., Tardieu, M., Ciron, C., Moullier, P., Parkes, J., Kline, K. L., Maire, I., Vanier, M. T., Heard, J. M., Colle, M. A. :
Safe, efficient, and reproducible gene therapy of the brain in the dog models of Sanfilippo and Hurler syndromes Mol Ther, 2011 ; 19 (2) : 251-259
Mamchaoui, K., Trollet, C., Bigot, A., Negroni, E., Chaouch, S., Wolff, A., Kandalla, P. K., Marie, S., Di Santo, J., Lacau St Guily, J., Muntoni, F., Kim, J., Philippi, S., Spuler, S., Levy, N., Blumen, S. C., Voit, T., Wright, W. E., Aamiri, A., Butler-Browne, G. S., Mouly, V. :
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders Skelet Muscle, 2011 ; 1 (1) : 34
Treves, S., Vukcevic, M., Jeannet, P. Y., Levano, S., Girard, T., Urwyler, A., Fischer, D., Voit, T., Jungbluth, H., Lillis, S., Muntoni, F., Quinlivan, R., Sarkozy, A., Bushby, K., Zorzato, F. :
Enhanced excitation coupled Ca2+ entry induces nuclear translocation of NFAT and contributes to IL-6 release from myotubes from patients with Central core disease Hum Mol Genet, 2011 ; 20 (3) : 589-600
Bertrand, A, Chikhaoui, K, Benyaou, R., Bonne, G. :
Clinical and genetic heterogeneity in laminopathies Biochem Soc Trans, 2011 ; 39 (6) : 1687-92