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Familial olivopontocerebellar atrophy with neonatal onset: a recessively inherited syndrome with systemic and biochemical abnormalities.

  • Published:1988-03-01 Issue:3 Volume:51 Page:385-390
  • ISSN:0022-3050
  • Container-title:Journal of Neurology, Neurosurgery & Psychiatry
  • language:en
  • Short-container-title:Journal of Neurology, Neurosurgery & Psychiatry

Author:

Harding B N,Dunger D B,Grant D B,Erdohazi M

Publisher

BMJ

Subject

Psychiatry and Mental health,Clinical Neurology,Surgery

Reference19 articles.

1. L'atrophie olivo-pontocerebelleuse;J, I.Dejerine; A, Thomas;Nouv Iconogr Salpet

2. Beitrag zur Kenntnis der hereditaren Ataxien und Kleinhirnatrophie;Menzel, P.;Arch Psychiatr Nervenkr

3. The oliovopontocerebellar atrophies: A review;Konigsmark, B.W.; Weiner, L.P.;Medicine,1970

4. Glutamate dehydrogenase deficiency in 3 patients with spinocerebellar syndrome;Plaitakis, A.; Nicklas, W.J.; Desnick, R.J.;Ann Neurol,1980

5. Pathology of olivopontocerebellar atrophy with glutamate dehydrogenase deficiency;Chouroverty, S.; Khedekar, R.; Derby, B.;Neurology,1984

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4. Congenital Disorders of Glycosylation with Emphasis on Cerebellar Involvement;Seminars in Neurology;2014-09-05

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