Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.

@article{Abele1997AutosomalDC,
  title={Autosomal dominant cerebellar ataxia type I. Nerve conduction and evoked potential studies in families with SCA1, SCA2 and SCA3.},
  author={M. Abele and Katrin Buerk and Frank Andres and Helge Roland Topka and Franco Laccone and Sylvia M. Boesch and Alexis Brice and G{\'e}raldine Cancel and Johannes Dichgans and Thomas Klockgether},
  journal={Brain : a journal of neurology},
  year={1997},
  volume={120 ( Pt 12)},
  pages={2141-8}
}
Forty-one patients suffering from autosomal dominant cerebellar ataxia type I (ADCA-I) were subjected to a genotype-phenotype correlation analysis using molecular genetic assignment to the spinocerebellar ataxia type 1, 2 or 3 (SCA1, -2 or -3) genetic locus, clinical examination and nerve conduction as well as evoked potential studies. Pyramidal tract signs, pale discs, and dysphagia were more frequent in SCA1 compared with SCA2 and SCA3 patients, while double vision occurred less frequently… CONTINUE READING