CareLit · DOI-Nachweis · Aktuelle Neurologie
Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6
DOI 10.1055/s-0028-1086589
Bibliografische Angaben
Nachweis in CareLit
Autor:innenL Schöls, C Globas, T Schmitz-Hübsch, D Timmann, S Szymanski, A Dürr, C Dupont, B Melegh, C Mariotti, S Boesch, B van de Warrenburg, A Filla, M Rakowicz, T Klockgether, S Tezenas du Montcel, P Bauer
ZeitschriftAktuelle Neurologie
Ausgabe09/2008
Jahrgang / SeitenNicht angegeben
Kernaussage aus der Literatur
Abstract-Vorschau
Onset of genetically determined neurodegenerative diseases is difficult to specify due to the insidious and slowly progressive nature of these disorders. This is especially true for spinocerebellar ataxia (SCA) because of varying affection of many parts of the nervous system and huge variability of symptoms. We investigated early symptoms in 287 patients with SCA1, SCA2, SCA3 or SCA6 and calculated the influence of…
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Zitierempfehlung
L Schöls, C Globas, T Schmitz-Hübsch, D Timmann, S Szymanski, A Dürr, C Dupont, B Melegh, C Mariotti, S Boesch, B van de Warrenburg, A Filla, M Rakowicz, T Klockgether, S Tezenas du Montcel, P Bauer (2008) Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6. Aktuelle Neurologie (09). https://doi.org/10.1055/s-0028-1086589
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