Articles dans des revues avec comité de lecture (263)
  1. 205. Ross, B. M., Eder, K., Moszczynska, A., Mamalias, N., Lamarche, J., Ang, L., Pandolfo, M., Rouleau, G., Kirchgessner, M., & Kish, S. J. (2000). Abnormal activity of membrane phospholipid synthetic enzymes in the brain of patients with Friedreich's ataxia and spinocerebellar atrophy type-1. Movement disorders, 15(2), 294-300. doi:10.1002/1531-8257(200003)15:2<294::AID-MDS1013>3.0.CO;2-D
  2. 206. Xiong, L., Labuda, M., Li, D. S., Hudson, T. J., Desbiens, R., Patry, G., Verret, S., Langevin, P., Mercho, S., Seni, M. H., Scheffer, I. E., Dubeau, F., Berkovic, S. F., Andermann, F., Andermann, E., & Pandolfo, M. (1999). Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12. American journal of human genetics, 65(6), 1698-1710. doi:10.1086/302649
  3. 207. 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.
  4. 208. Pandolfo, M. (1999). Molecular pathogenesis of Friedreich ataxia. Archives of neurology, 56(10), 1201-1208.
  5. 209. 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.
  6. 210. 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.
  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. 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
  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. 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
  11. 215. 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.
  12. 216. 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.
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