The natural history of spinocerebellar ataxia type 1, 2, 3, and 6

Authors :: Jacobi, H.
Bauer, P.
Giunti, P.
Labrum, R.
Sweeney, M.G.
Charles, P.
Dürr, A.
Marelli, C.
Globas, C.
Linnemann, C.
Schöls, L.
Rakowicz, M.
Rola, R.
Zdzienicka, E.
Schmitz-Hübsch, T.
Fancellu, R.
Mariotti, C.
Tomasello, C.
Baliko, L.
Melegh, B.
Filla, A.
Rinaldi, C.
van de Warrenburg, B.P.
Verstappen, C.C.P.
Szymanski, S.
Berciano, J.
Infante, J.
Timmann, D.
Boesch, S.
Hering, S.
Depondt, C.
Pandolfo, M.
Kang, J.-S.
Ratzka, S.
Schulz, J.
Tezenas du Montcel, S.
Klockgether, T.
Source :: Neurology (Ovid); September 2011, Vol. 77 Issue: 11 p1035-1041, 7p
Publication Year :: 2011
Abstract: 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.

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