Articles dans des revues avec comité de lecture (263)
  1. 97. 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. 98. Hourez, R., Servais, L., Orduz Perez, D., Gall, D., Millard, I., de Kerchove d'Exaerde, A., Chéron, G., Orr, H. T., Pandolfo, M., & Schiffmann, S. N. (2011). Aminopyridines Correct Early Dysfunction and Delay Neurodegeneration in a Mouse Model of Spinocerebellar Ataxia Type 1. The Journal of neuroscience, 31(33), 11795-11807. doi:10.1523/​JNEUROSCI.0905-11.2011
  3. 99. 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. 100. 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
  5. 101. 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
  6. 102. Fonteyn, E. M. R., Schmitz-Hübsch, T., Verstappen, C. C., Baliko, L., Bloem, B. R., Boesch, S., Bunn, L., Charles, P., Dürr, A., Filla, A., Giunti, P., Globas, C., Klockgether, T., Melegh, B., Pandolfo, M., De Rosa, A., Schöls, L., Timmann, D., Munneke, M., Kremer, B., & van de Warrenburg, B. P. (2010). Falls in spinocerebellar ataxias: Results of the EuroSCA Fall Study. Cerebellum, 9(2), 232-239. doi:10.1007/s12311-010-0155-z
  7. 103. 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. 104. Schulz, J. B., Borkert, J., Wolf, S., Schmitz-Hübsch, T., Klockgether, T., Rakowicz, M., Mariotti, C., Schöls, L., Timmann, D., van de Warrenburg, B. P. C., Dürr, A., Pandolfo, M., Kang, J. S., Mandly, A. G., Nägele, T., Hauser, T.-K., Grisoli, M., Boguslawska, R., & Bauer, P. (2010). Corrigendum to "Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6" [NeuroImage 49 (2010) 158-168] (DOI:10.1016/j.neuroimage.2009.07.027). NeuroImage, 50(4), 1712. doi:10.1016/j.neuroimage.2010.01.066
  9. 105. 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
  10. 106. Jäderstad, J., Jäderstad, L. M., Li, J., Chintawar, S., Salto, C., Pandolfo, M., Ourednik, V., Teng, Y. D., Sidman, R. L., Arenas, E., Snyder, E. Y., & Herlenius, E. (2010). Communication via gap junctions underlies early functional and beneficial interactions between grafted neural stem cells and the host. Proceedings of the National Academy of Sciences of the United States of America, 107(11), 5184-5189. doi:10.1073/pnas.0915134107
  11. 107. Schulz, J. B., Borkert, J., Wolf, S., Schmitz-Hübsch, T., Rakowicz, M., Mariotti, C., Schoels, L., Timmann, D., van de Warrenburg, B. P., Dürr, A., Pandolfo, M., Kang, J.-S., Mandly, A. G., Nägele, T., Grisoli, M., Boguslawska, R., Bauer, P., Klockgether, T., & Hauser, T.-K. (2010). Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6. NeuroImage, 49(1), 158-168. doi:10.1016/j.neuroimage.2009.07.027
  12. 108. Sirén, A., Polvi, A., Chahine, L., Labuda, M., Bourgoin, S., Anttonen, A.-K., Kousi, M., Hirvonen, K., Simola, K. O. J., Andermann, E., Laiho, A., Soini, J., Koivikko, M., Laaksonen, R., Pandolfo, M., & Lehesjoki, A.-E. (2010). Suggestive evidence for a new locus for epilepsy with heterogeneous phenotypes on chromosome 17q. Epilepsy research, 88(1), 65-75. doi:10.1016/j.eplepsyres.2009.09.022
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