Articles dans des revues avec comité de lecture (112)
  1. 68. Legros, B., Depondt, C., Levy Nogueira, M., Ligot, N., Mavroudakis, N., Naeije, G., & Gaspard, N. (2013). Intravenous Lacosamide in Refractory Seizure Clusters and Status Epilepticus: Comparison of 200 and 400 mg Loading Doses. Neurocritical care. doi:10.1007/s12028-013-9882-6
  2. 69. Massager, N., Tugendhaft, P., Depondt, C., Coppens, T., Drogba, K. L., Benmebarek, N. Y., De Witte, O., Van Bogaert, P., & Legros, B. (2013). Long-term outcome of surgical disconnection of the epileptic zone as an alternative to resection for nonlesional mesial temporal epilepsy. Journal of neurology, neurosurgery and psychiatry. doi:10.1136/jnnp-2012-304083
  3. 70. Depondt, C. (2013). Pharmacogénétique de l'épilepsie - Science ou fiction ? MS. Médecine sciences, 29(2), 189-193. doi:10.1051/medsci/2013292017
  4. 71. Kasperavičiūtė, D., Pandolfo, M., Depondt, C., et al. (2013). Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A. Brain, 136, 2040-2050. doi:10.1093/brain/awt233
  5. 72. Hitomi, Y., Heinzen, E. L., Donatello, S., Dahl, H.-H., Damiano, J. A., McMahon, J. M., Berkovic, S. F., Scheffer, I. E., Legros, B., Rai, M., Weckhuysen, S., Suls, A., de Jonghe, P., Pandolfo, M., Goldstein, D. B., Van Bogaert, P., & Depondt, C. (2013). Mutations in TNK2 in severe autosomal recessive infantile-onset epilepsy. Annals of neurology, 74(3), 496-501. doi:10.1002/ana.23934
  6. 73. Chinthapalli, K., Bartolini, E., Novy, J., Suttie, M., Marini, C., Falchi, M., Fox, Z., Clayton, L. M. S., Sander, J. W., Guerrini, R., Depondt, C., Hennekam, R., Hammond, P., & Sisodiya, S. M. (2012). Atypical face shape and genomic structural variants in epilepsy. Brain, 135(Pt 10), 3101-3114. doi:10.1093/brain/aws232
  7. 74. Pandolfo, M., Depondt, C., & Huppke, P. (2012). Periventricular heterotopia: Identifying homogeneity among heterogeneity. Neurology. doi:10.1212/WNL.0b013e31826aad7d
  8. 75. Heinzen, E., Depondt, C., Cavalleri, G. L., Ruzzo, E. K., Walley, N. M., Need, A. C., Ge, D., He, M., Cirulli, E. T., Zhao, Q., Cronin, K. D., Gumbs, C. E., Campbell, C. R., Hong, L. K., Maia, J. M., Shianna, K. V., McCormack, M., Radtke, R. A., O'Conner, G. D., Mikati, M. A., Gallentine, W. B., Husain, A. M., Sinha, S. R., Chinthapalli, K., Puranam, R. S., McNamara, J. O., Ottman, R., Sisodiya, S. M., Delanty, N., & Goldstein, D. B. (2012). Exome sequencing followed by large-scale genotyping fails to identify single rare variants of large effect in idiopathic generalized epilepsy. American journal of human genetics, 91(2), 293-302. doi:10.1016/j.ajhg.2012.06.016
  9. 76. Stein, J. L., Pandolfo, M., Depondt, C., et al. (2012). Identification of common variants associated with human hippocampal and intracranial volumes. Nature genetics, 44, 552–561. doi:10.1038/ng.2250
  10. 77. McCormack, M., Urban, T. J., Shianna, K. V., Walley, N., Pandolfo, M., Depondt, C., Chaila, E., O'Conner, G. D., Kasperavičiūtė, D., Radtke, R. A., Heinzen, E., Sisodiya, S. M., Delanty, N., & Cavalleri, G. L. (2012). Genome-wide mapping for clinically relevant predictors of lamotrigine- and phenytoin-induced hypersensitivity reactions. Pharmacogenomics, 13(4), 399-405. doi:10.2217/pgs.11.165
  11. 78. Naeije, G., Gaspard, N., Depondt, C., Pepersack, T., & Legros, B. (2012). Acute confusional state of unknown cause in the elderly: a study with continuous EEG monitoring. Epilepsy & behavior, 23(3), 330-334. doi:10.1016/j.yebeh.2012.01.023
  12. 79. Cirulli, E. T., Urban, T. J., Marino, S. E., Linney, K. N., Birnbaum, A. K., Depondt, C., Attix, D. K., Radtke, R. A., & Goldstein, D. B. (2012). Genetic and environmental correlates of topiramate-induced cognitive impairment. Epilepsia, 53(1), e5-e8. doi:10.1111/j.1528-1167.2011.03322.x
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