Literature DB >> 5832261

Ultrastructural lesions in rabbit hereditary ataxia.

J L O'Leary, A B Harris, R R Fox, J M Smith, M Tidwell.   

Abstract

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Year:  1965        PMID: 5832261     DOI: 10.1001/archneur.1965.00470030018002

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


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  5 in total

1.  Enzyme changes in the hereditary ataxic rabbit.

Authors:  N Robinson
Journal:  Acta Neuropathol       Date:  1970       Impact factor: 17.088

2.  Familial ataxia of the rabbit Sawin-Anders type. Ultrastructural analysis of degeneration of the cochlear nuclei.

Authors:  J L O'Leary; R R Fox; J M Smith; J Inukai
Journal:  Acta Neuropathol       Date:  1974       Impact factor: 17.088

3.  Cerebellar degeneration in thiamine-deficient rats.

Authors:  G H Collins; W K Converse
Journal:  Am J Pathol       Date:  1970-02       Impact factor: 4.307

4.  Status spongiosus of CNS and hepatic changes induced by cuprizone (biscyclohexanone oxalyldihydrazone).

Authors:  K Suzuki; Y Kikkawa
Journal:  Am J Pathol       Date:  1969-02       Impact factor: 4.307

5.  [New hereditary disease of the laboratory rabbit].

Authors:  E Osetowska
Journal:  Acta Neuropathol       Date:  1967-07-05       Impact factor: 17.088

  5 in total

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