Literature DB >> 13410569

Familial, central, areolar, choroidal atrophy of autosomal dominant inheritance.

K SANDVIG.   

Abstract

Entities:  

Keywords:  CHOROID/diseases

Mesh：

Year:  1955        PMID： 13410569     DOI： 10.1111/j.1755-3768.1955.tb05111.x

Source DB:  PubMed          Journal:  Acta Ophthalmol (Copenh)        ISSN： 0001-639X


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  6 in total

1.  Electroretinograms and pattern visually evoked cortical potentials in central areolar choroidal dystrophy.

Authors:  E Adachi-Usami; K Murayama; Y Yamamoto
Journal:  Doc Ophthalmol       Date:  1990-08       Impact factor: 2.379

2.  Bibliography of human genetics.

Authors:  R H POST
Journal:  Am J Hum Genet       Date:  1958-06       Impact factor: 11.025

3.  The development of central areolar choroidal dystrophy.

Authors:  C B Hoyng; A F Deutman
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1996-02       Impact factor: 3.117

4.  Choroidal atrophy. Clinical and genetic types.

Authors:  K Sandvig
Journal:  J Med Genet       Date:  1970-09       Impact factor: 6.318

5.  Polymorphous presentations in vitelliform macular dystrophy: subretinal neovascularisation and central choroidal atrophy.

Authors:  K G Noble; B M Scher; R E Carr
Journal:  Br J Ophthalmol       Date:  1978-08       Impact factor: 4.638

6.  Fluorescein angiography of the hereditary choroidal dystrophies.

Authors:  K G Noble; R E Carr; I M Siegel
Journal:  Br J Ophthalmol       Date:  1977-01       Impact factor: 4.638
  6 in total

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