Literature DB >> 5309737

Hereditary retinoschisis and early hemeralopia. A report of two cases.

J E MacVicar, H R Wilbrandt.   

Abstract

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Year:  1970        PMID： 5309737     DOI： 10.1001/archopht.1970.00990030629020

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


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  5 in total

1.  Diagnostic features of the Favre-Goldmann syndrome.

Authors:  G A Fishman; L M Jampol; M F Goldberg
Journal:  Br J Ophthalmol       Date:  1976-05       Impact factor: 4.638

2.  An Arg311Gln NR2E3 mutation in a family with classic Goldmann-Favre syndrome.

Authors:  S H Chavala; A Sari; H Lewis; G J T Pauer; E Simpson; S A Hagstrom; E I Traboulsi
Journal:  Br J Ophthalmol       Date:  2005-08       Impact factor: 4.638

3.  [Multimodal imaging in Goldmann-Favre syndrome].

Authors:  D Valler; M Ulbig; C P Lohmann; M Maier
Journal:  Ophthalmologe       Date:  2018-10       Impact factor: 1.059

4.  Retinitis pigmentosa: clinical observations and correlations.

Authors:  R C Pruett
Journal:  Trans Am Ophthalmol Soc       Date:  1983

5.  Goldmann-Favre syndrome in a four-year-old-girl.

Authors:  K Izumi; M Matsuhashi
Journal:  Doc Ophthalmol       Date:  1987-06       Impact factor: 2.379
  5 in total

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