Literature DB >> 13789353

Ophthalmoplegia and retinal degeneration associated with spinocerebellar ataxia.

R S JAMPEL, H OKAZAKI, H BERNSTEIN.   

Abstract

Entities:  

Keywords:  ATAXIA/complications; OCULOMOTOR PARALYSIS/etiology; RETINA/diseases

Mesh：

Year:  1961        PMID： 13789353     DOI： 10.1001/archopht.1961.00960010249017

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


× No keyword cloud information.
  12 in total

1.  Plasma vitamin A and beta-carotene in retinitis pigmentosa.

Authors:  W H Massoud; A C Bird; E S Perkins
Journal:  Br J Ophthalmol       Date:  1975-04       Impact factor: 4.638

2.  A family with sex linked optic atrophy : Ophthalmological and neurological aspects.

Authors:  H J Völker-Dieben; G H Van Lith; L N Went; J W Klawer; A Staal; E C De Vries-De Mol
Journal:  Doc Ophthalmol       Date:  1974-11       Impact factor: 2.379

3.  Chronic progressive external ophthalmoplegia and pigmentary degeneration of the retina.

Authors:  P V Mills; D I Bowen; D S Thomson
Journal:  Br J Ophthalmol       Date:  1971-05       Impact factor: 4.638

4.  Saccadic velocity measurements in strabismus.

Authors:  H S Metz
Journal:  Trans Am Ophthalmol Soc       Date:  1983

5.  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

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

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

7.  [Typical retinitis pigmentosa with chronic progressive external ophthalmoplegia (author's transl)].

Authors:  F Körner; I Probst
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1975-06-06

8.  Spastic paraplegia, optic atrophy, microcephaly with normal intelligence, and XY sex reversal: a new autosomal recessive syndrome?

Authors:  A S Teebi; S Miller; H Ostrer; P Eydoux; C Colomb-Brockmann; K Oudjhane; G Watters
Journal:  J Med Genet       Date:  1998-09       Impact factor: 6.318

9.  A syndrome of congenital retinal dystrophy and saccade palsy--a subset of Leber's amaurosis.

Authors:  A T Moore; D S Taylor
Journal:  Br J Ophthalmol       Date:  1984-06       Impact factor: 4.638

10.  [Investigations of peripheral and central somatosensory pathways in peroneal muscular atrophy and Friedreich's heredoataxia (author's transl)].

Authors:  M Sauer
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1980
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.