Articles dans des revues avec comité de lecture (79)
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Deconinck, N., Scaillon, M., Segers, V., Groswasser, J., & Dan, B. (2006). Opsoclonus-myoclonus associated with celiac disease. Pediatric neurology, 34(4), 312-314. doi:10.1016/j.pediatrneurol.2005.08.03469.
Pelc, K., Deconinck, N., Monier, A., Sekhara, T., Bormans, J., & Dan, B. (2006). Un nouveau cadre conceptuel pour l'infirmité motrice cérébrale. Revue médicale de Bruxelles, 27 Spec No, Sp33-37.70.
Pelc, K., Deconinck, N., Monier, A., Sekhara, T., & Dan, B. (2006). Un nouveau cadre conceptuel pour l’infirmité motrice cérébrale. Journal du Pédiatre Belge,(27), 33-37.71.
Deconinck, N., Duprez, T., Des Portes, V., Ghariani, S., Sindic, C., & Sébire, G. (2003). Familial bilateral medial parietooccipital band heterotopia not related to DCX or LIS1 gene defects. Neuropediatrics, 34(4), 146-148.73.
Deconinck, N., Tinsley, J., Kahn, D., Phelps, S., Fisher, R. R., Davies, K., & Gillis, J. M. (1998). Expression of full-length utrophin prevents muscular dystrophy in mdx mice. Nature medicine, 4(12), 1441-1445.74.
Goudemant, J. F., Deconinck, N., Tinsley, J., Demeure, R., Robert, A., Davies, K., & Gillis, J. M. (1998). Expression of truncated utrophin improves pH recovery in exercising muscles of dystrophic mdx mice: a 31P NMR study. Neuromuscular disorders, 8(6), 371-379.76.
Deconinck, N., Tinsley, J., De Backer, F., Kahn, D., Phelps, S., Fisher, R. R., Davies, K., & Gillis, J. M. (1997). Expression of truncated utrophin leads to major functional improvements in dystrophin-deficient muscles of mice. Nature medicine, 3(11), 1216-1221.78.
Deconinck, N., Ragot, T., Marechal, G., Perricaudet, M., & Gillis, J. M. (1996). Functional protection of dystrophic mouse (mdx) muscles after adenovirus-mediated transfer of a dystrophin minigene. Proceedings of the National Academy of Sciences of the United States of America, 93, 3570-3574.