Articles dans des revues avec comité de lecture (110)

  1. 56. Depondt, C. (2016). Copy number variants in absence epilepsy. Neurology: Genetics, 2(2), e67. doi:10.1212/NXG.0000000000000067
  2. 57. 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
  3. 58. 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
  4. 59. 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
  5. 60. 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
  6. 61. 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
  7. 62. 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
  8. 63. 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
  9. 64. 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
  10. 65. 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
  11. 66. 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
  12. 67. 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

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