Articles dans des revues avec comité de lecture (263)
  1. 181. Van Bogaert, P., Aeby, A., Hennart, H., Pandolfo, M., & Verheulpen, D. (2004). Electro-clinical study of infantile seizures in a family with hemiplegic migraine and epilepsy. Epilepsia, 45(Supplément S3), 192. doi:10.1111/j.1528-1157.2004.tb04927.x
  2. 182. Hu, S., Labuda, M., Pandolfo, M., Goss, G. G., McDermid, H. E., & Ali, D. W. (2003). Variants of the KCNMB3 regulatory subunit of maxi BK channels affect channel inactivation. Physiological genomics (Print), 15(3), 191-198. doi:10.1152/physiolgenomics.00110.2003
  3. 183. Wiener, V., Honnorat, J., Pandolfo, M., Kentos, A., & Manto, M. (2003). Myorhythmia associated with Hodgkin's lymphoma. Journal of neurology, 250(11), 1382-1384. doi:10.1007/s00415-003-0203-4
  4. 184. Pandolfo, M. (2003). Friedreich ataxia. Seminars in pediatric neurology, 10(3), 163-172.
  5. 185. Bertelli, M., Gallo, S., Cecchin, S., Garofalo, P. G., & Pandolfo, M. (2003). Ricerca di mutazione nel gene CLCN2 (canale del cloro 2) in 130 pazienti con epilessia idiopatica focale e generalizzata. Bollettino - Lega italiana contro l'epilessia,(121-122), 125-130.
  6. 186. Manto, M., Pandolfo, M., & Moore, J. (2003). Bilateral high-frequency synchronous discharges: a new form of tremor in humans. Archives of neurology, 60(3), 416-422.
  7. 187. Santos, M. M., Miranda, C., Levy, J. E., Montross, L. K., Cossée, M., Sequeiros, J., Andrews, N., Koenig, M., & Pandolfo, M. (2003). Iron metabolism in mice with partial frataxin deficiency. Cerebellum, 2(2), 146-153. doi:10.1080/14734220309408
  8. 188. Pandolfo, M. (2002). Frataxin deficiency and mitochondrial dysfunction. Mitochondrion, 2(1-2), 87-93.
  9. 189. Gallagher, C. L., Waclawik, A. J., Beinlich, B. R., Harding, C. O., Pauli, R. M., Poirer, J., Pandolfo, M., & Salamat, M. S. (2002). Friedreich's ataxia associated with mitochondrial myopathy: clinicopathologic report. Journal of child neurology, 17(6), 453-456.
  10. 190. Silveira, I., Miranda, C., Guimarães, L., Moreira, M.-C., Alonso, I., Mendonça, P., Ferro, A., Pinto-Basto, J., Coelho, J., Ferreirinha, F., Poirier, J., Parreira, E., Vale, J., Januário, C., Barbot, C., Tuna, A., Barros, J., Koide, R., Tsuji, S., Holmes, S. E., Margolis, R. L., Jardim, L., Pandolfo, M., Coutinho, P., & Sequeiros, J. (2002). Trinucleotide repeats in 202 families with ataxia: a small expanded (CAG)n allele at the SCA17 locus. Archives of neurology, 59(4), 623-629.
  11. 191. Vokaer, M., Bier, J. C., Elincx, S., Claes, T., Paquier, P., Goldman, S., Bartholomé, E., & Pandolfo, M. (2002). The cerebellum may be directly involved in cognitive functions. Neurology, 58(6), 967-970.
  12. 192. Matsuura, T., Ranum, L. P. W., Volpini, V., Pandolfo, M., Sasaki, H., Tashiro, K., Watase, K., Zoghbi, H. Y., & Ashizawa, T. (2002). Spinocerebellar ataxia type 10 is rare in populations other than Mexicans. Neurology, 58(6), 983-984.
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