Articles dans des revues avec comité de lecture (262)
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  2. 206. Ohshima, K., Sakamoto, N., Labuda, M., Poirier, J., Moseley, M. L., Montermini, L., Ranum, L. P. W., Wells, R. D., & Pandolfo, M. (1999). A nonpathogenic GAAGGA repeat in the Friedreich gene: implications for pathogenesis. Neurology, 53(8), 1854-1857.
  3. 207. Pandolfo, M. (1999). Molecular pathogenesis of Friedreich ataxia. Archives of neurology, 56(10), 1201-1208.
  4. 208. Li, D. S., Ohshima, K., Jiralerspong, S., Bojanowski, M. W., & Pandolfo, M. (1999). Knock-out of the cyaY gene in Escherichia coli does not affect cellular iron content and sensitivity to oxidants. FEBS letters, 456(1), 13-16.
  5. 209. Sakamoto, N., Chastain, P. D., Parniewski, P., Ohshima, K., Pandolfo, M., Griffith, J. D., & Wells, R. D. (1999). Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxia. Molecular cell, 3(4), 465-475.
  6. 210. Kish, S. J., Mastrogiacomo, F., Guttman, M., Furukawa, Y., Taanman, J. W., Dozić, S., Pandolfo, M., Lamarche, J., DiStefano, L., & Chang, L. J. (1999). Decreased brain protein levels of cytochrome oxidase subunits in Alzheimer's disease and in hereditary spinocerebellar ataxia disorders: A nonspecific change? Journal of neurochemistry, 72(2), 700-707. doi:10.1046/j.1471-4159.1999.0720700.x
  7. 211. Cossée, M., Dürr, A., Schmitt, M., Dahl, N., Trouillas, P., Allinson, P., Kostrzewa, M., Nivelon-Chevallier, A., Gustavson, K. H., Kohlschütter, A., Müller, U., Mandel, J. L., Brice, A., Koenig, M., Cavalcanti, F., Tammaro, A., De Michele, G., Filla, A., Cocozza, S., Labuda, M., Montermini, L., Poirier, J., & Pandolfo, M. (1999). Friedreich's ataxia: Point mutations and clinical presentation of compound heterozygotes. Annals of neurology, 45(2), 200-206. doi:10.1002/1531-8249(199902)45:2<200::AID-ANA10>3.0.CO;2-U
  8. 212. Poirier, J., Ohshima, K., & Pandolfo, M. (1999). Heteroduplexes may confuse the interpretation of PCR-based molecular tests for the Friedreich ataxia GAA triplet repeat. Human mutation, 13(4), 328-330. doi:10.1002/(SICI)1098-1004(1999)13:4<328::AID-HUMU10>3.0.CO;2-J
  9. 213. Pandolfo, M. (1999). Friedreich's ataxia: clinical aspects and pathogenesis. Seminars in neurology, 19(3), 311-321. doi:10.1055/s-2008-1040847
  10. 214. Moseley, M. L., Benzow, K. A., Schut, L. J., Bird, T. D., Gomez, C. M., Barkhaus, P. E., Blindauer, K. A., Labuda, M., Pandolfo, M., Koob, M. D., & Ranum, L. P. W. (1998). Incidence of dominant spinocerebellar and Friedreich triplet repeats among 361 ataxia families. Neurology, 51(6), 1666-1671.
  11. 215. Kish, S. J., Lopes-Cendes, I., Guttman, M., Furukawa, Y., Pandolfo, M., Rouleau, G. A., Ross, B. M., Nance, M., Schut, L., Ang, L., & DiStefano, L. (1998). Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders. Archives of neurology, 55(10), 1299-1304.
  12. 216. Zara, F., Labuda, M., Garofalo, P. G., Durisotti, C., Bianchi, A., Castellotti, B., Patel, P. I., Avanzini, G., & Pandolfo, M. (1998). Unusual EEG pattern linked to chromosome 3p in a family with idiopathic generalized epilepsy. Neurology, 51(2), 493-498.
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