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Familial olivopontocerebellar atrophy with macular degeneration: a separate entity among the olivopontocerebellar atrophies

  • Published:2009-01-29 Issue:2 Volume:73 Page:180-190
  • ISSN:0001-6314
  • Container-title:Acta Neurologica Scandinavica
  • language:en
  • Short-container-title:

Author:

Anttinen A.,Nikoskelainen E.,Marttila R. J.,Grenman R.,Falck B.,Aarnisalo E.,Kalimo H.

Publisher

Wiley

Subject

Neurology (clinical),Neurology,General Medicine

Reference27 articles.

1. The olivopontocerebellar atrophies;Plaitakis;Semin Neurol,1982

2. The olivopontocerebellar atrophies: a review;Konigsmark;Medicine (Baltimore),1970

3. Classification of the hereditary ataxias and paraplegias;Harding;Lancet,1983

4. Do visual evoked potentials give relevant information to the neuro-ophthalmological examination in optic nerve lesions;Nikoskelainen;Acta Neurol Scand,1982

5. AEEGS' clinical evoked potential guidelines. Recommended standards for short-latency auditory evoked potentials;Coats;J Clin Neurophysiol,1984

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3. Spinocerebellar ataxia type 7 (SCA7) – correlations between phenotype and genotype in one large Belgian family;Journal of the Neurological Sciences;1999-09

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