Literature DB >> 6021917

Hereditary olivopontocerebellar atrophy with retinal degeneration. Report of a family through six generations.

L P Weiner, B W Konigsmark, J Stoll, J W Magladery.   

Abstract

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Year:  1967        PMID： 6021917     DOI： 10.1001/archneur.1967.00470220028004

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


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

Authors:  B N Harding; D B Dunger; D B Grant; M Erdohazi
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-03       Impact factor: 10.154

3.  On an autosomal dominant form of retinal-cerebellar degeneration: an autopsy study of five patients in one family.

Authors:  J J Martin; N Van Regemorter; L Krols; J M Brucher; T de Barsy; H Szliwowski; P Evrard; C Ceuterick; M J Tassignon; H Smet-Dieleman
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

4.  Retinitis pigmentosa, ataxia, and peripheral neuropathy.

Authors:  R R Tuck; J G McLeod
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-03       Impact factor: 10.154
  4 in total

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