Literature DB >> 6052813

[Progressive nuclear ophthalmoplegia and hereditary spinal cerebellar degeneration. Study of 1 anatomo-clinical case].

S Brion, J De Recondo.   

Abstract

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Year:  1967        PMID： 6052813

Source DB:  PubMed          Journal:  Rev Neurol (Paris)        ISSN： 0035-3787            Impact factor:   2.607


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  3 in total

1.  Hereditary spastic ataxia with congenital miosis: four cases in one family.

Authors:  D J Dick; P K Newman; P G Cleland
Journal:  Br J Ophthalmol       Date:  1983-02       Impact factor: 4.638

2.  Genetic aspects of autosomal dominant late onset cerebellar ataxia.

Authors:  A E Harding
Journal:  J Med Genet       Date:  1981-12       Impact factor: 6.318

3.  Autosomal recessive late onset multisystem disorder with cerebellar cortical atrophy at necropsy: report of a family.

Authors:  A E Harding; J V Diengdoh; A J Lees
Journal:  J Neurol Neurosurg Psychiatry       Date:  1984-08       Impact factor: 10.154
  3 in total

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