Articles dans des revues avec comité de lecture (263)
  1. 193. Miranda, C., Santos, M. M., Ohshima, K., Smith, J. F., Li, L., Bunting, M., Cossée, M., Koenig, M., Sequeiros, J., Kaplan, J., & Pandolfo, M. (2002). Frataxin knockin mouse. FEBS letters, 512(1-3), 291-297.
  2. 194. Pandolfo, M., Manto, M., & Lubicz, B. (2002). Cerebellar atrophy with hypercupremia: a new recessive ataxia. Neurology, 58(3), 36.
  3. 195. Pandolfo, M. (2002). Iron metabolism and mitochondrial abnormalities in Friedreich ataxia. Blood cells, molecules, & diseases, 29(3), 536-47; discussion 548-52.
  4. 196. Pandolfo, M., Blecic, S., Mavroudakis, N., Van Bogaert, P., Paquier, P., Manto, M., & Zegers De Beyl, D. (2002). Le Service de Neurologie. Revue médicale de Bruxelles, 23 Suppl 2, 127-130.
  5. 197. Jiralerspong, S., Ge, B., Hudson, T. J., & Pandolfo, M. (2001). Manganese superoxide dismutase induction by iron is impaired in Friedreich ataxia cells. FEBS letters, 509(1), 101-105.
  6. 198. Pandolfo, M. (2001). Molecular basis of Friedreich ataxia. Movement disorders, 16(5), 815-821. doi:10.1002/mds.1162
  7. 199. Mazarib, A., Xiong, L., Neufeld, M. Y., Birnbaum, M., Korczyn, A. D., Pandolfo, M., & Berkovic, S. F. (2001). Unverricht-Lundborg disease in a five-generation Arab family: instability of dodecamer repeats. Neurology, 57(6), 1050-1054.
  8. 200. Santos, M. M., Ohshima, K., & Pandolfo, M. (2001). Frataxin deficiency enhances apoptosis in cells differentiating into neuroectoderm. Human molecular genetics, 10(18), 1935-1944.
  9. 201. Sakamoto, N., Larson, J. E., Iyer, R. R., Montermini, L., Pandolfo, M., & Wells, R. D. (2001). GGA*TCC-interrupted triplets in long GAA*TTC repeats inhibit the formation of triplex and sticky DNA structures, alleviate transcription inhibition, and reduce genetic instabilities. The Journal of biological chemistry, 276(29), 27178-27187. doi:10.1074/jbc.M101852200
  10. 202. Sakamoto, N., Ohshima, K., Montermini, L., Pandolfo, M., & Wells, R. D. (2001). Sticky DNA, a self-associated complex formed at long GAA*TTC repeats in intron 1 of the frataxin gene, inhibits transcription. The Journal of biological chemistry, 276(29), 27171-27177. doi:10.1074/jbc.M101879200
  11. 203. Emond, M., Lepage, G., Vanasse, M., & Pandolfo, M. (2000). Increased levels of plasma malondialdehyde in Friedreich ataxia. Neurology, 55(11), 1752-1753.
  12. 204. Pandolfo, M. (2000). The molecular basis of Friedreich ataxia. Neurología, 15(8), 325-329.
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