par Jacobi, Heike;Bauer, Peter;Giunti, P;Labrum, R;Sweeney, M G;Charles, P;Dürr, A;Marelli, C;Globas, C;Linnemann, C;Schöls, Lüdger;Rakowicz, M;Rola, R;Zdzienicka, E;Schmitz-Hübsch, T;Fancellu, Roberto;Mariotti, Christian;Tomasello, C;Baliko, L;Melegh, Bela;Filla, A;Rinaldi, Carlo;van de Warrenburg, B P;Verstappen, Carla C;Szymanski, S;Berciano, J;Infante, J;Timmann, D;Boesch, S;Hering, S;Depondt, Chantal ;Pandolfo, Massimo ;Kang, J-S;Ratzka, Susanne;Schulz, Jörg Bernhard;Tezenas du Montcel, Sophie;Klockgether, T
Référence Neurology, 77, 11, page (1035-1041)
Publication Publié, 2011-09
Référence Neurology, 77, 11, page (1035-1041)
Publication Publié, 2011-09
Article révisé par les pairs
Résumé : | To obtain quantitative data on the progression of the most common spinocerebellar ataxias (SCAs) and identify factors that influence their progression, we initiated the EUROSCA natural history study, a multicentric longitudinal cohort study of 526 patients with SCA1, SCA2, SCA3, or SCA6. We report the results of the 1- and 2-year follow-up visits. |