Literature DB >> 6821680

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

D J Dick, P K Newman, P G Cleland.   

Abstract

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Year:  1983        PMID: 6821680      PMCID: PMC1039974          DOI: 10.1136/bjo.67.2.97

Source DB:  PubMed          Journal:  Br J Ophthalmol        ISSN: 0007-1161            Impact factor:   4.638


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  21 in total

1.  Hereditary spastic ataxia with central retinal degeneration and vestibular impairment. A clinical report on a family.

Authors:  M BERGSTEDT; S JOHANSSON; R MULLER
Journal:  Neurology       Date:  1962-02       Impact factor: 9.910

2.  Ophthalmoplegia and retinal degeneration associated with spinocerebellar ataxia.

Authors:  R S JAMPEL; H OKAZAKI; H BERNSTEIN
Journal:  Arch Ophthalmol       Date:  1961-08

3.  A sex-linked recessive form of spastic paraplegia.

Authors:  A W JOHNSTON; V A McKUSICK
Journal:  Am J Hum Genet       Date:  1962-03       Impact factor: 11.025

4.  Familial spastic paraplegia; its relation to mental and cardiac abnormalities.

Authors:  J M SUTHERLAND
Journal:  Lancet       Date:  1957-07-27       Impact factor: 79.321

5.  Hereditary cerebellar ataxia; olivopontocerebellar type.

Authors:  J H CHANDLER; J BEBIN
Journal:  Neurology       Date:  1956-03       Impact factor: 9.910

6.  Hereditary ataxia with optic atrophy of the retrobulbar neuritis type, and latent pallido-luysian degeneration.

Authors:  M ANDRE-VAN LEEUWEN; L VAN BOGAERT
Journal:  Brain       Date:  1949-09       Impact factor: 13.501

7.  Familial spastic paraplegia with retinal degeneration.

Authors:  M Mahloudji; P O Chuke
Journal:  Johns Hopkins Med J       Date:  1968-09

8.  Oculocerebrorenal syndrome of Lowe. A case report.

Authors:  N F Fisher; J Hallett; G Carpenter
Journal:  Arch Ophthalmol       Date:  1967-05

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

Authors:  L P Weiner; B W Konigsmark; J Stoll; J W Magladery
Journal:  Arch Neurol       Date:  1967-04

10.  The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.

Authors:  A E Harding
Journal:  Brain       Date:  1982-03       Impact factor: 13.501

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  3 in total

1.  [A refractory pupil].

Authors:  M Koch; S Lindner; A Langmann
Journal:  Ophthalmologe       Date:  2006-08       Impact factor: 1.059

2.  Megalocornea. Clinical and genetic aspects.

Authors:  F M Meire
Journal:  Doc Ophthalmol       Date:  1994       Impact factor: 2.379

3.  Ultrabiomicroscopic-histopathologic correlations in individuals with autosomal dominant congenital microcoria: three-generation family report.

Authors:  Arturo Ramirez-Miranda; Juan M Paulin-Huerta; Eduardo Chavez-Mondragón; Gilberto Islas-de la Vega; Abelardo Rodriguez-Reyes
Journal:  Case Rep Ophthalmol       Date:  2011-05-13
  3 in total

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