Articles dans des revues avec comité de lecture (288)
  1. 96. Noël, X., Billieux, J., Van der Linden, M., Dan, B., Hanak, C., de Bournonville, S., Baurain, C., & Verbanck, P. (2009). Impaired inhibition of proactive interference in abstinent individuals with alcoholism. Neuropsychology, development, and cognition. Section A, Journal of clinical and experimental neuropsychology, 31(1), 57-64. doi:10.1080/13803390801982726
  2. 97. Chéron, G., Cebolla Alvarez, A. M., Petieau, M., Bengoetxea, A., Palmero Soler, E., Leroy, A., & Dan, B. (2009). Adaptive changes of rhythmic EEG oscillations in space implications for brain-machine interface applications. International review of neurobiology, 86, 171-187. doi:10.1016/S0074-7742(09)86013-3
  3. 98. Kornreich, C., Desaive, P., & Dan, B. (2009). Delayed Onset Parkinsonism in Alcoholic Patient following ARDS: Alcoholism could be a risk factor. The Open Addiction Journal, 2, 28-29.
  4. 99. Bahi-Buisson, N., Roze, E., Dionisi, C., Escande, F., Valayannopoulos, V., Feillet, F., Heinrichs, C., Chadefaux-Vekemans, B., Dan, B., & de Lonlay, P. (2008). Neurological aspects of hyperinsulinism-hyperammonaemia syndrome. Developmental medicine and child neurology, 50(12), 945-949. doi:10.1111/j.1469-8749.2008.03114.x
  5. 100. Bahi-Buisson, N., Rozen, E., El Sabbagh, S., Dionisi, C., Escande, F., Grandin, L., Heinrichs, C., Kim, I., Valayannopoulos, V., Boddaert, N., Dan, B., Feuillet, F., Dulac, O., Plouin, P., & de Lonlay, P. (2008). Neurological outcome of patients with hyperinsulinemic hyperammonaemia syndrome: a putative relation with the genotype. Developmental medicine and child neurology, 50(12), 945-949. doi:10.1111/j.1469-8749.2008.03114.x
  6. 101. Dan, B. (2008). The paediatrician's role in support groups for rare diseases. Acta paediatrica, 97(11), 1510-1511. doi:10.1111/j.1651-2227.2008.01041.x
  7. 102. 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
  8. 103. Pelc, K., Chéron, G., & Dan, B. (2008). Behavior and neuropsychiatric manifestations in Angelman syndrome. Neuropsychiatric Disease and Treatment (Print), 4(3), 577-584.
  9. 104. Pelc, K., Chéron, G., Boyd, S. G., & Dan, B. (2008). Are there distinctive sleep problems in Angelman syndrome? Sleep Medicine, 9(4), 434-441. doi:10.1016/j.sleep.2007.07.001
  10. 105. Beetz, C., Schüle, R., Deconinck, T., Tran-Viet, K.-N., Zhu, H., Kremer, B., Frints, S. G. M., van Zelst-Stams, W. A. G., Byrne, P., Otto, S., Nygren, A. O. H., Baets, J., Smets, K., Ceulemans, B., Dan, B., Nagan, N., Kassubek, J., Klimpe, S., Klopstock, T., Stolze, H., Smeets, H. J. M., Schrander-Stumpel, C. T. R. M., Hutchinson, M., van de Warrenburg, B. P., Braastad, C., Deufel, T., Pericak-Vance, M. A., Schöls, L., de Jonghe, P., & Züchner, S. (2008). REEP1 mutation spectrum and genotype/phenotype correlation in hereditary spastic paraplegia type 31. Brain, 131(Pt 4), 1078-1086. doi:10.1093/brain/awn026
  11. 106. Pelc, K., Boyd, S. G., Chéron, G., & Dan, B. (2008). Epilepsy in Angelman syndrome. Seizure, 17(3), 211-217. doi:10.1016/j.seizure.2007.08.004
  12. 107. Chéron, G., Servais, L., & Dan, B. (2008). Cerebellar network plasticity: from genes to fast oscillation. Neuroscience, 153(1), 1-19. doi:10.1016/j.neuroscience.2008.01.074
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