Articles dans des revues avec comité de lecture (263)
  1. 109. Rai, M., Soragni, E., Chou, C. J., Barnes, G., Jones, S., Rusche, J. R., Gottesfeld, J. M., & Pandolfo, M. (2010). Two new pimelic diphenylamide HDAC inhibitors induce sustained frataxin upregulation in cells from Friedreich's ataxia patients and in a mouse model. PloS one, 5(1), e8825. doi:10.1371/journal.pone.0008825
  2. 110. Marmolino, D., Manto, M., Acquaviva, F., Vergara, P., Ravella, A. B., Monticelli, A., & Pandolfo, M. (2010). PGC-1alpha down-regulation affects the antioxidant response in Friedreich's ataxia. PloS one, 5(4), e10025. doi:10.1371/journal.pone.0010025
  3. 111. Anesi, L., De Gemmis, P., Pandolfo, M., & Hladnik, U. (2010). Two Novel Homozygous SACS Mutations in Unrelated Patients Including the First Reported Case of Paternal UPD as an Etiologic Cause of ARSACS. Journal of molecular neuroscience, 43, 346-349. doi:10.1007/s12031-010-9448-4
  4. 112. Chintawar, S., Hourez, R., Ravella, A. B., Gall, D., Orduz Perez, D., Rai, M., Bishop, D. P., Geuna, S., Schiffmann, S. N., & Pandolfo, M. (2009). Grafting neural precursor cells promotes functional recovery in an SCA1 mouse model. The Journal of neuroscience, 29(42), 13126-13135. doi:10.1523/JNEUROSCI.0647-09.2009
  5. 113. Lemmens, R., Abboud, S., Robberecht, W., Vanhees, L., Pandolfo, M., Thijs, V., & Goris, A. (2009). Variant on 9p21 strongly associates with coronary heart disease, but lacks association with common stroke. European journal of human genetics, 17(10), 1287-1293. doi:10.1038/ejhg.2009.42
  6. 114. Chintawar, S., Hourez, R., Ravella, A. B., Gall, D., Orduz Perez, D., Rai, M., Bishop, D. P., Geuna, S., Schiffmann, S. N., & Pandolfo, M. (2009). Grafting neural precursor cells promotes functional recovery in an SCA1 mouse model. The Journal of neuroscience, 29(42), 13126-13135. doi:10.1523/JNEUROSCI.0647-09.2009
  7. 115. Del Bo, R., Ghezzi, S., Corti, S., Pandolfo, M., Ranieri, M., Santoro, D., Ghione, I., Prelle, A., Orsetti, V., Mancuso, M., Sorarù, G., Briani, C., Angelini, C., Siciliano, G., Bresolin, N., & Comi, G. P. (2009). TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations. European journal of neurology, 16(6), 727-732. doi:10.1111/j.1468-1331.2009.02574.x
  8. 116. Schulz, J. B., Boesch, S., Bürk, K., Dürr, A., Giunti, P., Mariotti, C., Pousset, F., Schöls, L., Vankan, P., & Pandolfo, M. (2009). Diagnosis and treatment of Friedreich ataxia: a European perspective. Nature reviews. Neurology, 5(4), 222-234. doi:10.1038/nrneurol.2009.26
  9. 117. Chintawar, S., Cayrol, R., Antel, J., Pandolfo, M., & Prats, A. C. (2009). Blood-brain barrier promotes differentiation of human fetal neural precursor cells. Stem cells, 27(4), 838-846. doi:10.1002/stem.25
  10. 118. Pandolfo, M., & Pastore, A. (2009). The pathogenesis of Friedreich ataxia and the structure and function of frataxin. Journal of neurology, 256 Suppl 1, 9-17. doi:10.1007/s00415-009-1003-2
  11. 119. Pandolfo, M. (2009). Friedreich ataxia: the clinical picture. Journal of neurology, 256 Suppl 1, 3-8. doi:10.1007/s00415-009-1002-3
  12. 120. Kearney, M., Orrell, R. W., Fahey, M., & Pandolfo, M. (2009). Antioxidants and other pharmacological treatments for Friedreich ataxia. Cochrane database of systematic reviews (Online),(4), CD007791. doi:10.1002/14651858.CD007791.pub2
    13. << Précédent 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 Suivant >>