Articles dans des revues avec comité de lecture (84)
  1. 56. Rymen, D., Keldermans, L., Race, V., Régal, L., Deconinck, N., Dionisi-Vici, C., Fung, C.-W., Sturiale, L., Rosnoblet, C., Foulquier, F., Matthijs, G., & Jaeken, J. (2012). COG5-CDG: Expanding the clinical spectrum. Orphanet journal of rare diseases, 7(1), 94. doi:10.1186/1750-1172-7-94
  2. 57. Al Husni Al Keilani, M., Carlier, S., Groswasser, J., Dan, B., & Deconinck, N. (2011). Rett syndrome associated with continuous spikes and waves during sleep. Acta neurologica belgica, 111(4), 328-332.
  3. 58. Baijot, S., Deconinck, N., Massat, I., Slama, H., & Colin, C. (2011). Behavioral and neurophysiological study of attentional and inhibitory processes in ADHD and control children with a continuous performance task. 3rd International Congress on ADHD. Attention Deficit and Hyperactivity Disorders, 3(2), 208.
  4. 59. Goban, V., François, A., Chaouat, P., Cogan, N., Guissard, G., & Deconinck, N. (2011). Encéphalopathie de Gayet-Wernicke et anorexie mentale, présentation clinique particulière chez un adolescent. Neuropsychiatrie de l'enfance et de l'adolescence, 59, 428-432. doi:10.1016/j.neurenf.2011.06.002
  5. 60. Wang, C. C., Bönnemann, C. C., Rutkowski, A., Sejersen, T., Bellini, J., Battista, V., Florence, J. J., Schara, U., Schuler, P. P., Wahbi, K., Aloysius, A., Bash, R. R., Béroud, C., Bertini, E., Bushby, K., Cohn, R. R., Connolly, A., Deconinck, N., Desguerre, I., Eagle, M., Estournet-Mathiaud, B., Ferreiro, A., Fujak, A., Goemans, N., Iannaccone, S. S., Jouinot, P., Main, M., Melacini, P., Mueller-Felber, W., Muntoni, F., Nelson, L. L., Rahbek, J., Quijano-Roy, S., Sewry, C. C., Storhaug, K., Simonds, A. K., Tseng, B., Vajsar, J., Vianello, A., & Zeller, R. (2010). Consensus statement on standard of care for congenital muscular dystrophies. Journal of child neurology, 25(12), 1559-1581. doi:10.1177/0883073810381924
  6. 61. Prigogine, C., Richard, P., Van Den Bergh, P., Groswasser, J., & Deconinck, N. (2010). Novel LMNA mutation presenting as severe congenital muscular dystrophy. Pediatric neurology, 43(4), 283-286. doi:10.1016/j.pediatrneurol.2010.05.016
  7. 62. Deconinck, N., Yaou, R. B., Eymard, B., Payan, C. A. M. C., Voit, T., Dion, E., Bonne, G., Briñas, L., Allamand, V., Ferreiro, A., Stojkovic, T., Guicheney, P., & Richard, P. (2010). Differentiating Emery-Dreifuss muscular dystrophy and collagen VI-related myopathies using a specific CT scanner pattern. Neuromuscular disorders, 20(8), 517-523. doi:10.1016/j.nmd.2010.04.009
  8. 63. Dachy, B., Deltenre, P., Deconinck, N., & Dan, B. (2010). The H reflex as a diagnostic tool for Miller Fisher syndrome in pediatric patients. Journal of clinical neuroscience, 17(3), 410-411. doi:10.1016/j.jocn.2009.06.014
  9. 64. Bourreau, Y., Roux, S., Gomot, M., Bonnet Brilhault, F., Barthelemy, C., Soncarrieu, D., & Deconinck, N. (2010). Validation of the repetitive and restricted behaviour scale in autism spectrum disorders. European child & adolescent psychiatry.
  10. 65. Deconinck, N., & Stojkovic, T. (2009). Ullrich congenital dystrophy and bethlem myopathy: Current knowledge on the clinical spectrum, pathogenesis, and future therapeutic avenues of collagen VI related muscular dystrophies. Current Pediatric Reviews, 5(1), 28-35. doi:10.2174/157339609787587573
  11. 66. Coutelier, M., Andries, S., Ghariani, S., Dan, B., Duyckaerts, C., van Rijckevorsel, K., Raftopoulos, C., Deconinck, N., Sonderegger, P., Scaravilli, F., Vikkula, M., & Godfraind, C. (2008). Neuroserpin mutation causes electrical status epilepticus of slow-wave sleep. Neurology, 71(1), 64-66. doi:10.1212/01.wnl.0000316306.08751.28
  12. 67. Deconinck, N. (2008). Neuroanatomie des troubles articulaires chez l’enfant IMOC. Rééducation orthophonique,(233), 35-44.
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