Publications (1181)

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
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
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
Bertrand, A, Chikhaoui, K, Benyaou, R., Bonne, G. :
Clinical and genetic heterogeneity in laminopathies Biochem Soc Trans, 2011 ; 39 (6) : 1687-92
Hernandez-Lain, A., Husson, I., Monnier, N., Farnoux, C., Brochier, G., Lacene, E., Beuvin, M., Viou, M. T., Manere, L., Claeys, K. G., Fardeau, M., Lunardi, J., Voit, T., Romero, N. B. :
De novo RYR1 heterozygous mutation (I4898T) causing lethal core-rod myopathy in twins Eur J Med Genet, 2011 ; 54 (1) : 29-33
Meyer-Schwesinger, C., Meyer, T. N., Sievert, H., Hoxha, E., Sachs, M., Klupp, E. M., Munster, S., Balabanov, S., Carrier, L., Helmchen, U., Thaiss, F., Stahl, R. A. :
Ubiquitin C-terminal hydrolase-l1 activity induces polyubiquitin accumulation in podocytes and increases proteinuria in rat membranous nephropathy Am J Pathol, 2011 ; 178 (5) : 2044-57
Cavalcante, P., Maggi, L., Colleoni, L., Caldara, R., Motta, T., Giardina, C., Antozzi, C., Berrih-Aknin, S., Bernasconi, P., Mantegazza, R. :
Inflammation and epstein-barr virus infection are common features of myasthenia gravis thymus: possible roles in pathogenesis Autoimmune Dis, 2011 ; (SP) :