Spinocerebellar ataxia

Citations 1-4 of 4 total displayed.

Most recent content (11 Sep 2007):

ARTICLES
Eye movement abnormalities in spinocerebellar ataxia type 17 (SCA17)

J. Hübner, A. Sprenger, C. Klein, J. Hagenah, H. Rambold, C. Zühlke, D. Kömpf, A. Rolfs, H. Kimmig, and C. Helmchen
Neurology 2007; 69: 1160-1168. [Abstract] [Full text] [PDF]  

Past content (since Mar 2003):

CLINICAL/SCIENTIFIC NOTES
LIMBIC ENCEPHALITIS AS PRESENTATION OF A SAP DEFICIENCY

H. Verhelst, R. Van Coster, N. Bockaert, G. Laureys, S. Latour, A. Fischer, and F. Haerynck
Neurology 2007; 69: 218-219. [Full text] [PDF]  

ARTICLES
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

B. P.C. van de Warrenburg, D. S. Verbeek, S. J. Piersma, F. A.M. Hennekam, P. L. Pearson, N. V.A.M. Knoers, H. P.H. Kremer, and R. J. Sinke
Neurology 2003; 61: 1760-1765. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Phenotypic variability of aprataxin gene mutations

C. Tranchant, M. Fleury, M. C. Moreira, M. Koenig, and J. M. Warter
Neurology 2003; 60: 868-870. [Abstract] [Full text] [PDF]