Articles dans des revues avec comité de lecture (109)
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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.x81.
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-z82.
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.2369883.
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/NEJMoa101329784.
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/awq13085.
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.2010.03.00286.
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.2010.03.01887.
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.2274088.
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.0b013e3181d1a6c989.
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.2008.09.00390.
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.2228891.
Schmitz-Hübsch, T., Coudert, M., Bauer, P., Giunti, P., Globas, C., Baliko, L., Filla, A., Mariotti, C., Rakowicz, M., Charles, P., Ribai, P., Szymanski, S., Infante, J., van de Warrenburg, B. P., Dürr, A., Timmann, D., Boesch, S., Fancellu, R., Rola, R., Depondt, C., Schöls, L., Zdienicka, E., Kang, J.-S., Döhlinger, S., Kremer, B., Stephenson, D. A., Melegh, B., Pandolfo, M., di Donato, S., du Montcel, S. T., & Klockgether, T. (2008). Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms. Neurology, 71(13), 982-989. doi:10.1212/01.wnl.0000325057.33666.72