Articles dans des revues avec comité de lecture (84)
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Seferian, A. M., Moraux, A., Canal, A., Decostre, V., Diebate, O., Le Moing, A.-G., Gidaro, T., Deconinck, N., Van Parys, F., Vereecke, W., Wittevrongel, S., Annoussamy, M., Mayer, M., Maincent, K., Cuisset, J. M., Tiffreau, V., Denis, S., Jousten, V., Quijano-Roy, S., Voit, T., Hogrel, J.-Y., & Servais, L. (2015). Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial. PloS one, 10(4), e0121799. doi:10.1371/journal.pone.012179945.
Seferian, A. M., Moraux, A., Annoussamy, M., Canal, A., Decostre, V., Diebate, O., Le Moing, A.-G., Gidaro, T., Deconinck, N., Van Parys, F., Vereecke, W., Wittevrongel, S., Mayer, M., Maincent, K., Desguerre, I., Thémar-Noel, C., Cuisset, J. M., Tiffreau, V., Denis, S., Jousten, V., Quijano-Roy, S., Voit, T., Hogrel, J.-Y., & Servais, L. (2015). Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial. PloS one, 10(2), e0113999. doi:10.1371/journal.pone.011399946.
Kissine, M., Cano-Chevrel, J., Carlier, S., De Brabanter, P., Ducenne, L., Pairon, M.-C., Deconinck, N., Delvenne, V., & Leybaert, J. (2015). Children with Autism Understand Indirect Speech Acts: Evidence from a Semi-Structured Act-Out Task. PloS one, 10(11), e0142191. doi:10.1371/journal.pone.014219147.
Voit, T., Topaloglu, H., Straub, V., Muntoni, F., Deconinck, N., Campion, G., De Kimpe, S. J., Eagle, M., Guglieri, M., Hood, S., Liefaard, L., Lourbakos, A., Morgan, A., Nakielny, J., Quarcoo, N., Ricotti, V., Rolfe, K., Servais, L., Wardell, C., Wilson, R., Wright, P., & Kraus, J. E. (2014). Safety and efficacy of drisapersen for the treatment of Duchenne muscular dystrophy (DEMAND II): an exploratory, randomised, placebo-controlled phase 2 study. Lancet neurology, 13(10), 987-996. doi:10.1016/S1474-4422(14)70195-448.
Van Schil, K., Meire, F., Karlstetter, M., Bauwens, M., Verdin, H., Coppieters, F., Scheiffert, E., Van Nechel, C., Langmann, T., Deconinck, N., & De Baere, E. (2014). Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion. Genetics in medicine. doi:10.1038/gim.2014.9549.
Clumeck, C., Suarez Garcia, S., Bourguignon, M., Wens, V., Op De Beeck, M., Marty, B., Deconinck, N., Soncarrieu, M.-V., Goldman, S., Jousmaki, V., Van Bogaert, P., & De Tiege, X. (2014). Preserved Coupling between the Reader's Voice and the Listener's Cortical Activity in Autism Spectrum Disorders. PloS one, 9(3), e92329. doi:10.1371/journal.pone.009232950.
Amrom, D., Hamdan, F. F., Michaud, J. J., Tanyalçin, I., Lissens, W., Verhelst, H., Deconinck, N., Brouhard, G. G., Décarie, J. C., Vanderhasselt, T., Das, S. J. S., & Jansen, A. C. M. A. (2014). Polymicrogyria with dysmorphic basal ganglia? Think tubulin! Clinical genetics, 85(2), 178-183. doi:10.1111/cge.1214151.
Bönnemann, C. C., Wang, C. C., Quijano-Roy, S., Deconinck, N., Bertini, E., Ferreiro, A., Muntoni, F., Sewry, C. C., Béroud, C., Mathews, K. K., Moore, S. S., Bellini, J., Rutkowski, A., & North, K. K. (2014). Diagnostic approach to the congenital muscular dystrophies. Neuromuscular disorders, 24(4), 289-311. doi:10.1016/j.nmd.2013.12.01152.
Foley, R. A., Quijano-Roy, S., Collins, J., Straub, V., McCallum, M., Deconinck, N., Mercuri, E., Pane, M., D'Amico, A., Bertini, E., North, K., Ryan, M., Richard, P., Allamand, V., Hicks, D., Lamandé, S., Hu, Y., Gualandi, F., Auh, S., Muntoni, F., & Bönnemann, C. C. (2013). Natural history of pulmonary function in collagen VI-related myopathies. Brain, 136(Pt 12), 3625-3633. doi:10.1093/brain/awt28454.
Baijot, S., Colin, C., Slama, H., Söderlund, G., Dan, B., & Deconinck, N. (2013). Why an apparent distraction would help ADHD children ? Attention Deficit and Hyperactivity Disorders, 5(2), 134.55.
Rymen, D., Keldermans, L., Race, V., Matthijs, G., Régal, L., Jaeken, J., Deconinck, N., Dionisi-Vici, C., Fung, C.-W., Sturiale, L., Rosnoblet, C., & Foulquier, F. (2013). Erratum: COG5-CDG: Expanding the clinical spectrum (Orphanet Journal of Rare Diseases (2013) 8 (120)). Orphanet journal of rare diseases, 8(1), 120. doi:10.1186/1750-1172-8-120