Articles dans des revues avec comité de lecture (263)
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van de Warrenburg, B. P., van Gaalen, J., Boesch, S., Burgunder, J.-M., Dürr, A., Giunti, P., Klockgether, T., Mariotti, C., Pandolfo, M., & Riess, O. (2014). EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood. European journal of neurology. doi:10.1111/ene.1234164.
Béjot, Y., Aboa-Eboulé, C., Debette, S., Pezzini, A., Tatlisumak, T., Engelter, S., Grond-Ginsbach, C., Touzé, E., Sessa, M., Metso, T., Metso, A., Kloss, M., Caso, V., Dallongeville, J., Lyrer, P., Leys, D., Giroud, M., Pandolfo, M., Abboud, S., & CADISP Group, (2014). Characteristics and outcomes of patients with multiple cervical artery dissection. Stroke, 45(1), 37-41. doi:10.1161/STROKEAHA.113.00165465.
Matilla-Dueñas, A., Ashizawa, T., Brice, A., Magri, S., McFarland, K. N., Pandolfo, M., Pulst, S. M., Riess, O., Rubinsztein, D. C., Schmidt, J., Schmidt, T. H., Scoles, D. R., Stevanin, G., Taroni, F., Underwood, B. R., & Sánchez, I. (2013). Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias. Cerebellum. doi:10.1007/s12311-013-0539-y66.
Grond-Ginsbach, C., Giossi, A., Aksay, S. S., Engelter, S., Lyrer, P., Metso, T., Metso, A., Tatlisumak, T., Debette, S., Leys, D., Thijs, V., Bersano, A., Abboud, S., Kloss, M., Lichy, C., Grau, A. A., Pezzini, A., Touzé, E., Pandolfo, M., Thijs, V., Metso, T., Metso, A., Bodenant, M., Debette, S., Ossou, P., Louillet, F., Mas, J.-L., Leder, S., Léger, A., Deltour, S., Crozier, S., Méresse, I., & Samson, Y. (2013). Elevated peripheral leukocyte counts in acute cervical artery dissection. European journal of neurology, 20(10), 1405-1410. doi:10.1111/ene.1220168.
Chahine, L., Abou-Khalil, B., Siren, A., Andermann, F., Hedera, P., Ge, Q., Andermann, E., & Pandolfo, M. (2013). A new locus for familial temporal lobe epilepsy on chromosome 3q. Epilepsy research, 106(3), 338-344. doi:10.1016/j.eplepsyres.2013.07.00769.
Sánchez, I., Piñol, P., Corral-Juan, M., Pandolfo, M., & Matilla-Dueñas, A. (2013). A novel function of Ataxin-1 in the modulation of PP2A activity is dysregulated in the spinocerebellar ataxia type 1. Human molecular genetics, 22(17), 3425-3437. doi:10.1093/hmg/ddt197