Articles dans des revues avec comité de lecture (110)
  1. 80. Jacobi, H., Bauer, P., Giunti, P., Labrum, R., Sweeney, M. G., Charles, P., Dürr, A., Marelli, C., Globas, C., Linnemann, C., Schöls, L., Rakowicz, M., Rola, R., Zdzienicka, E., Schmitz-Hübsch, T., Fancellu, R., Mariotti, C., Tomasello, C., Baliko, L., Melegh, B., Filla, A., Rinaldi, C., van de Warrenburg, B. P., Verstappen, C. C., Szymanski, S., Berciano, J., Infante, J., Timmann, D., Boesch, S., Hering, S., Depondt, C., Pandolfo, M., Kang, J.-S., Ratzka, S., Schulz, J. B., Tezenas du Montcel, S., & Klockgether, T. (2011). The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study. Neurology, 77(11), 1035-1041. doi:10.1212/WNL.0b013e31822e7ca0
  2. 81. Catarino, C. B., Kasperavičiūtė, D., Thom, M., Cavalleri, G. L., Martinian, L., Heinzen, E., Dorn, T., Grunwald, T., Chaila, E., Depondt, C., Krämer, G., Delanty, N., Goldstein, D. B., & Sisodiya, S. M. (2011). Genomic microdeletions associated with epilepsy: not a contraindication to resective surgery. Epilepsia, 52(8), 1388-1392. doi:10.1111/j.1528-1167.2011.03087.x
  3. 82. Jacobi, H., Hauser, T.-K., Giunti, P., Globas, C., Bauer, P., Schmitz-Hübsch, T., Balikó, L., Filla, A., Mariotti, C., Rakowicz, M., Charles, P., Ribaï, P., Szymanski, S., Infante, J., van de Warrenburg, B. P., Dürr, A., Timmann, D., Boesch, S., Fancellu, R., Rola, R., Depondt, C., Schöls, L., Zdzienicka, E., Kang, J.-S., Ratzka, S., Kremer, B., Stephenson, D. A., Melegh, B., Pandolfo, M., du Montcel, S. T., Borkert, J., Schulz, J. B., & Klockgether, T. (2011). Spinocerebellar Ataxia Types 1, 2, 3 and 6: the Clinical Spectrum of Ataxia and Morphometric Brainstem and Cerebellar Findings. Cerebellum. doi:10.1007/s12311-011-0292-z
  4. 83. Schmitz-Hübsch, T., Coudert, M., Tezenas du Montcel, S., Giunti, P., Labrum, R., Dürr, A., Ribaï, P., Charles, P., Linnemann, C., Schöls, L., Rakowicz, M., Rola, R., Zdzienicka, E., Fancellu, R., Mariotti, C., Balikó, L., Melegh, B., Filla, A., Salvatore, E., van de Warrenburg, B. P., Szymanski, S., Infante, J., Timmann, D., Boesch, S., Depondt, C., Kang, J.-S., Schulz, J. B., Klopstock, T., Lossnitzer, N., Löwe, B., Frick, C., Rottländer, D., Schlaepfer, T. E., & Klockgether, T. (2011). Depression comorbidity in spinocerebellar ataxia. Movement disorders, 26(5), 870-876. doi:10.1002/mds.23698
  5. 84. McCormack, M., Alfirevic, A., Bourgeois, S., Farrell, J., Kasperavičiūtė, D., Carrington, M., Sills, G., Marson, T., Jia, X., de Bakker, P., Chinthapalli, K., Molokhia, M., Johnson, M., O’Connor, G., Chaila, E., Alhusaini, S., Shianna, K., Radtke, R., Heinzen, E. L., Walley, N., Pandolfo, M., Pichler, W., Park, B., Depondt, C., Sisodiya, S. M., Goldstein, D. B., Deloukas, P., Delanty, N., Cavalleri, G. L., Pirmohamed, M., et al. (2011). HLA-A*3101 and Carbamazepine-Induced Hypersensitivity Reactions in Europeans. The New England journal of medicine, 364(12), 1134-1143. doi:10.1056/NEJMoa1013297
  6. 85. Kasperavičiūtė, D., Catarino, C. B., Heinzen, E., Depondt, C., Cavalleri, G. L., Caboclo, L. O., Tate, S. K., Jamnadas-Khoda, J., Chinthapalli, K., Clayton, L. M. S., Shianna, K. V., Radtke, R. A., Mikati, M. A., Gallentine, W. B., Husain, A. M., Alhusaini, S., Leppert, D., Middleton, L. T., Gibson, R. A., Johnson, M. R., Matthews, P. M., Hosford, D., Heuser, K., Amos, L., Ortega, M., Zumsteg, D., Wieser, H.-G., Steinhoff, B. J., Kramer, G., Hansen, J., Dorn, T., Kantanen, A.-M., Gjerstad, L., Peuralinna, T., Hernandez, D. G., Eriksson, K., Kalviainen, R., Doherty, C. P., Wood, N. W., Pandolfo, M., Duncan, J. S., Sander, J. W., Delanty, N., Goldstein, D. B., & Sisodiya, S. M. (2010). Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. Brain. doi:10.1093/brain/awq130
  7. 86. Naeije, G., de Hemptinne, Q., Depondt, C., Pandolfo, M., & Legros, B. (2010). Acute behavioural change in a young woman evolving towards cerebellar syndrome. Clinical neurology and neurosurgery, 112(6), 509-511. doi:10.1016/j.clineuro.2010.03.002
  8. 87. Heinzen, E., Radtke, R. A., Urban, T. J., Cavalleri, G. L., Depondt, C., Need, A. C., Walley, N., Nicoletti, P., Ge, D., Catarino, C. B., Duncan, J. S., Kasperavičiūtė, D., Tate, S. K., Caboclo, L. O., Sander, J. W., Clayton, L. M. S., Linney, K. N., Shianna, K. V., Gumbs, C., Smith, J., Cronin, K. D., Maia, J. M., Doherty, C. P., Pandolfo, M., Leppert, D., Middleton, L. T., Gibson, R. A., Johnson, M. R., Matthews, P. M., Hosford, D., Kalviainen, R., Eriksson, K., Kantanen, A.-M., Dorn, T., Hansen, J., Kramer, G., Steinhoff, B. J., Wieser, H.-G., Zumsteg, D., Ortega, M., Wood, N. W., Huxley-Jones, J., Mikati, M. A., Gallentine, W. B., Husain, A. M., Buckley, P. G., Stallings, R. L., Podgoreanu, M. V., Delanty, N., Sisodiya, S. M., & Goldstein, D. B. (2010). Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes. American journal of human genetics, 86(5), 707-718. doi:10.1016/j.ajhg.2010.03.018
  9. 88. Schmitz-Hübsch, T., Coudert, M., Giunti, P., Globas, C., Balikó, L., Fancellu, R., Mariotti, C., Filla, A., Rakowicz, M., Charles, P., Ribaï, P., Szymanski, S., Infante, J., van de Warrenburg, B. P., Dürr, A., Timmann, D., Boesch, S., Rola, R., Depondt, C., Schöls, L., Zdzienicka, E., Kang, J.-S., Ratzka, S., Kremer, B., Schulz, J. B., Klopstock, T., Melegh, B., du Montcel, S. T., & Klockgether, T. (2010). Self-rated health status in spinocerebellar ataxia--results from a European multicenter study. Movement disorders, 25(5), 587-595. doi:10.1002/mds.22740
  10. 89. Schmitz-Hübsch, T., Fimmers, R., Rakowicz, M., Rola, R., Zdzienicka, E., Fancellu, R., Mariotti, C., Linnemann, C., Schöls, L., Timmann, D., Filla, A., Salvatore, E., Infante, J., Giunti, P., Labrum, R., Kremer, B., van de Warrenburg, B. P., Balikó, L., Melegh, B., Depondt, C., Schulz, J. B., du Montcel, S. T., & Klockgether, T. (2010). Responsiveness of different rating instruments in spinocerebellar ataxia patients. Neurology, 74(8), 678-684. doi:10.1212/WNL.0b013e3181d1a6c9
  11. 90. Lynch, J. M., Tate, S. K., Kinirons, P., Weale, M. E., Cavalleri, G. L., Depondt, C., Murphy, K., O'Rourke, D., Doherty, C. P., Shianna, K. V., Wood, N. W., Sander, J. W., Delanty, N., Goldstein, D. B., & Sisodiya, S. M. (2009). No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy. Epilepsy research, 83(1), 44-51. doi:10.1016/j.eplepsyres.2008.09.003
  12. 91. Globas, C., du Montcel, S. T., Balikó, L., Boesch, S., Depondt, C., Didonato, S., Dürr, A., Filla, A., Klockgether, T., Mariotti, C., Melegh, B., Rakowicz, M., Ribaï, P., Rola, R., Schmitz-Hübsch, T., Szymanski, S., Timmann, D., van de Warrenburg, B. P., Bauer, P., & Schöls, L. (2008). Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Movement disorders, 23(15), 2232-2238. doi:10.1002/mds.22288
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