Articles dans des revues avec comité de lecture (262)
  1. 157. Lapucci, C., Montin, D. P., Pandolfo, M., & Bertelli, M. (2006). Real-time PCR and linkage studies to identify carriers presenting HPRT deleted gene. Molecular medicine, 12(9-10), 246-251. doi:10.2119/2005-00046.Lapucci
  2. 158. Pandolfo, M. (2006). Iron and Friedreich ataxia. Journal of neural transmission. Supplementum,(70), 143-146.
  3. 159. Pandolfo, M. (2006). Friedreich ataxia: Detection of GAA repeat expansions and frataxin point mutations. Methods in molecular medicine, 126, 197-216.
  4. 160. Oulad Ben Taib, N., Nordeyn, O. B. T., Manto, M., Mario, M., Pandolfo, M., Massimo, P., & Brotchi, J. (2005). Hemicerebellectomy blocks the enhancement of cortical motor output associated with repetitive somatosensory stimulation in the rat. Journal of physiology, 567(Pt 1), 293-300. doi:10.1113/jphysiol.2005.088229
  5. 161. Dagonnier, M., Laute, M.-A., Pandolfo, M., & Manto, M. (2005). Effects of levetiracetam on the production of nitric oxide--an in vivo study. Journal of neurology, 252(6), 727-730. doi:10.1007/s00415-005-0726-y
  6. 162. Pandolfo, M., & van de Warrenburg, B. P. (2005). Spinocerebellar ataxia type 14: opening a new door in dominant ataxia research? Neurology, 64(7), 1113-1114. doi:10.1212/01.WNL.0000160013.10806.53
  7. 163. Berkovic, S. F., Mazarib, A., Walid, S., Neufeld, M. Y., Manelis, J., Nevo, Y., Korczyn, A. D., Yin, J., Xiong, L., Pandolfo, M., Mulley, J. C., & Wallace, R. H. (2005). A new clinical and molecular form of Unverricht-Lundborg disease localized by homozygosity mapping. Brain, 128(Pt 3), 652-658. doi:10.1093/brain/awh377
  8. 164. Manto, M., Laute, M.-A., & Pandolfo, M. (2005). Depression of extra-cellular GABA and increase of NMDA-induced nitric oxide following acute intra-nuclear administration of alcohol in the cerebellar nuclei of the rat. Cerebellum, 4(4), 230-238. doi:10.1080/14734220500243835
  9. 165. Debray, C., Vereecken, P., Belot, N., Teillard, P., Brion, J. P., Pandolfo, M., & Pochet, R. (2004). Multifaceted role of galectin-3 on human glioblastoma cell motility. Biochemical and biophysical research communications, 325(4), 1393-1398. doi:10.1016/j.bbrc.2004.10.181
  10. 166. Badhwar, A., Jansen, A., Andermann, F., Pandolfo, M., & Andermann, E. (2004). Striking intrafamilial phenotypic variability and spastic paraplegia in the presence of similar homozygous expansions of the FRDA1 gene. Movement disorders, 19(12), 1424-1431. doi:10.1002/mds.20264
  11. 167. Lee, H.-Y., Xu, Y., Huang, Y., Ahn, A. H., Auburger, G. W. J., Pandolfo, M., Kwiecinski, H., Grimes, D. A., Lang, A. E., Nielsen, J. E., Averyanov, Y., Servidei, S., Friedman, A., Van Bogaert, P., Abramowicz, M., Bruno, M., Sorensen, B. F., Tang, L., Fu, Y.-H., & Ptácek, L. J. (2004). The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway. Human molecular genetics, 13(24), 3161-3170. doi:10.1093/hmg/ddh330
  12. 168. D'Agostino, D., Bertelli, M., Gallo, S., Cecchin, S., Albiero, E., Garofalo, P. G., Gambardella, A., St Hilaire, J.-M., Kwiecinski, H., Andermann, E., & Pandolfo, M. (2004). Mutations and polymorphisms of the CLCN2 gene in idiopathic epilepsy. Neurology, 63(8), 1500-1502.
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