Literature DB >> 13357958

Retinal degeneration in hereditary ataxia.

A BJORK, U LINDBLOM, L WADENSTEN.   

Abstract

Entities:  

Keywords:  DEGENERATION; HEREDITARY SPINAL SCLEROSIS; RETINA/diseases

Mesh：

Year:  1956        PMID： 13357958      PMCID： PMC497204          DOI： 10.1136/jnnp.19.3.186

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  2 in total

1.  Flicker electroretinography in some cases of total colour-blindness.

Authors:  L WADENSTEN
Journal:  Acta Ophthalmol (Copenh)       Date:  1954

2.  The use of flicker electroretinography in the human eye; observations on some normal and pathological retinae.

Authors:  E DODT; L WADENSTEN
Journal:  Acta Ophthalmol (Copenh)       Date:  1954
  2 in total
  9 in total

1.  Abiotrophic ophthalmoplegia externa.

Authors:  S I DAVIDSON
Journal:  Br J Ophthalmol       Date:  1960-10       Impact factor: 4.638

2.  Cone and cone-rod dystrophies.

Authors:  A T Moore
Journal:  J Med Genet       Date:  1992-05       Impact factor: 6.318

3.  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

Review 4.  The cone degenerations.

Authors:  A E Krill; A F Deutman; M Fishman
Journal:  Doc Ophthalmol       Date:  1973-04-16       Impact factor: 2.379

5.  Psychosocial genetics: an emerging scientific discipline.

Authors:  P S Harper
Journal:  J Med Genet       Date:  1993-07       Impact factor: 6.318

6.  Temporal aspects of the electroretinogram in cone-rod dystrophy.

Authors:  M Horiguchi; Y Miyake; K Yagasaki; K Ichikawa
Journal:  Doc Ophthalmol       Date:  1985-08-30       Impact factor: 2.379

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

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

Review 8.  Retinitis pigmentosa, pigmentary retinopathies, and neurologic diseases.

Authors:  M Tariq Bhatti
Journal:  Curr Neurol Neurosci Rep       Date:  2006-09       Impact factor: 5.081

9.  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
  9 in total

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