Publications (1181)

Deconinck, N., Stojkovic, T :
Ullrich Congenital Dystrophy and Bethlem Myopathy: Current Knowledge on the Clinical Spectrum, Pathogenesis, and Future Therapeutic Avenuesn of Collagen VI Related Muscular Dystrophies Curr Pediatr Rev, 2009 ; 5 : 28-35
Koenig, J., Bauche, S., Ben Ammar, A., Nicolle, D., Rigoard, P., Eymard, B., Hantai, D. :
Remaniements experimentaux et pathologiques de la jonction neuromusculaire Neurochirurgie, 2009 ; 55S1 : S104-S109
Payan, C. A., Hogrel, J. Y., Hammouda, E. H., Lacomblez, L., Ollivier, G., Doppler, V., Eymard, B., Attarian, S., Pouget, J., Desnuelle, C., Laforet, P. :
Periodic salbutamol in facioscapulohumeral muscular dystrophy: a randomized controlled trial Arch Phys Med Rehabil, 2009 ; 90 (7) : 1094-101
Bevilacqua, J A, Fardeau, M, Romero, NB :
« Necklace » fibers and « trilaminar » fibers are different. Reply Acta Neuropathol, 2009 ; 118 : 319-320
Durr, A., Gargiulo, M :
Diagnostiquer une maladie avant qu’elle ne soit visible Pour la Science, 2009 ; (383) : 57-59
Lourenco, S., Boni, S., Furling, D., Cosset, F. L., Cahour, A. :
A cell-based bicistronic lentiviral reporter system for identification of inhibitors of the hepatitis C virus internal ribosome entry site J Virol Methods, 2009 ; 158 (1-2) : 152-159
Stojkovic, T., Hammouda, E. H., Richard, P., de Munain, A. L., Ruiz-Martinez, J., Gonzalez, P. C., Laforet, P., Penisson-Besnier, I., Ferrer, X., Lacour, A., Lacomblez, L., Claeys, K. G., Maurage, C. A., Fardeau, M., Eymard, B. :
Clinical outcome in 19 French and Spanish patients with valosin-containing protein myopathy associated with Paget’s disease of bone and frontotemporal dementia Neuromuscul Disord, 2009 ; 19 (5) : 316-323
Ciron, C., Cressant, A., Roux, F., Raoul, S., Cherel, Y., Hantraye, P., Deglon, N., Schwartz, B., Barkats, M., Heard, J. M., Tardieu, M., Moullier, P., Colle, M. A. :
Human alpha-Iduronidase Gene Transfer Mediated by Adeno-Associated Virus Types 1, 2, and 5 in the Brain of Nonhuman Primates: Vector Diffusion and Biodistribution Hum Gene Ther, 2009 ; 20 (4) : 350-60
Haberlova, J., Claeys, K. G., De Jonghe, P., Seeman, P. :
Cranial nerves palsy as an initial feature of an early onset distal hereditary motor neuropathy – A new distal hereditary motor neuropathy phenotype Neuromuscul Disord, 2009 ; 19 (6) : 427-428
Moresi, V, Garcia-Alvarez, G, PristerĂ , A, Rizzuto, M, Rocchi, M, Marazzi, G, Sassoon, D, Coletti, D. :
Modulation of Caspase Activity Regulates Skeletal Muscle Regeneration and Function in Response to Vasopressin and Tumor Necrosis Factor PLoS ONE, 2009 ; 4 (5) : e5570