Articles dans des revues avec comité de lecture (112)
  1. 56. Bellante, F., Legros, B., Depondt, C., Creteur, J., Taccone, F., & Gaspard, N. (2016). Midazolam and thiopental for the treatment of refractory status epilepticus: a retrospective comparison of efficacy and safety. Journal of neurology, 263(4), 799-806. doi:10.1007/s00415-016-8074-7
  2. 57. Depondt, C. (2016). Copy number variants in absence epilepsy. Neurology: Genetics, 2(2), e67. doi:10.1212/NXG.0000000000000067
  3. 58. Linnemann, C., Rola, R., Klockgether, T., García, A., Mutlu, G., Schöls, L., Tezenas du Montcel, S., Rakowicz, M., Schmitz-Hübsch, T., Szymanski, S., Berciano, J., van de Warrenburg, B. P. C., Pedersen, K., & Depondt, C. (2016). Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6. Cerebellum, 15(2), 165-173. doi:10.1007/s12311-015-0684-6
  4. 59. Lamartine Sabido Monteiro, M., Taccone, F., Depondt, C., Lamanna, I., Gaspard, N., Ligot, N., Mavroudakis, N., Naeije, G., Vincent, J. L., & Legros, B. (2016). The Prognostic Value of 48-h Continuous EEG During Therapeutic Hypothermia After Cardiac Arrest. Neurocritical care, 24(2), 153-162. doi:10.1007/s12028-015-0215-9
  5. 60. Franke, B., Depondt, C., & Pandolfo, M. (2016). Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept. Nature neuroscience, 19(3), 420-431. doi:10.1038/nn.4228
  6. 61. Depondt, C., Donatello, S., Rai, M., Wang, F. C., Manto, M., Simonis, N., & Pandolfo, M. (2016). MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43). Neurology: Genetics, 2(5), e94. doi:10.1212/NXG.0000000000000094
  7. 62. Hibar, D. D., Depondt, C., Pandolfo, M., et al. (2015). Common genetic variants influence human subcortical brain structures. Nature (London), 520(7546), 224-229. doi:10.1038/nature14101
  8. 63. Reetz, K., Dogan, I., Costa, A. S., Dafotakis, M., Fedosov, K., Schulz, J. B., Giunti, P., Parkinson, M. M., Sweeney, M. M., Mariotti, C., Panzeri, M., Nanetti, L., Arpa, J., Sanz-Gallego, I., Dürr, A., Charles, P., Boesch, S., Nachbauer, W., Klopstock, T., Karin, I., Depondt, C., Pandolfo, M., vom Hagen, J. M., Schöls, L., Giordano, I. A., Klockgether, T., & Bürk, K. (2015). Biological and clinical characteristics of the European Friedreich's Ataxia Consortium for Translational Studies (EFACTS) cohort: A cross-sectional analysis of baseline data. Lancet neurology, 14(2), 174-182. doi:10.1016/S1474-4422(14)70321-7
  9. 64. Depondt, C., Donatello, S., Simonis, N., Rai, M., Van Heurck, R., Abramowicz, M., D'Hooghe, M., & Pandolfo, M. (2014). Autosomal recessive cerebellar ataxia of adult onset due to STUB1 mutations. Neurology. doi:10.1212/WNL.0000000000000416
  10. 65. Thompson, P. M., Depondt, C., Pandolfo, M., et al. (2014). The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data. Brain Imaging and Behavior, 8(2), 153-182. doi:10.1007/s11682-013-9269-5
  11. 66. du Montcel, S. T., Dufaure-Garé, I., Golmard, J. L., Dürr, A., Charles, P., Forlani, S., Marelli, C., Stevanin, G., Brice, A., Rakowicz, M., Nanetti, L., Mariotti, C., Sulek, A., Rola, R., Schöls, L., Bauer, P., Jacobi, H., Schmitz-Hübsch, T., Filla, A., Timmann, D., van de Warrenburg, B. P. C., Kang, J. S., Giunti, P., Cook, A., Baliko, L., Melegh, B., Boesch, S., Szymanski, S., Berciano, J., Infante, J., Buerk, K., Masciullo, M., Di Fabio, R., Depondt, C., Ratka, S., & Klockgether, T. (2014). Prediction of the age at onset in spinocerebellar ataxia type 1, 2, 3 and 6. Journal of medical genetics, 51(7), 479-486. doi:10.1136/jmedgenet-2013-102200
  12. 67. Naeije, G., Depondt, C., Meeus, C., Korpak, K., Pepersack, T., & Legros, B. (2014). EEG patterns compatible with nonconvulsive status epilepticus are common in elderly patients with delirium: A prospective study with continuous EEG monitoring. Epilepsy & behavior, 36, 18-21. doi:10.1016/j.yebeh.2014.04.012
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