Literature DB >> 14303336

UNILATERAL RETINAL DYSPLASIA.

W S HUNTER, L E ZIMMERMAN.   

Abstract

Entities:  

Keywords:  ABNORMALITIES; DIAGNOSIS; EYE DISEASES; GENETICS, HUMAN; NOMENCLATURE; PATHOLOGY; RETINA

Mesh：

Year:  1965        PMID： 14303336     DOI： 10.1001/archopht.1965.00970040025006

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


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  10 in total

1.  Linkage analysis of Norrie disease with X-chromosomal ornithine aminotransferase.

Authors:  J B Bateman
Journal:  Trans Am Ophthalmol Soc       Date:  1992

2.  Light and electron microscopic study of dysplastic rosette-like structures occurring in the disorganized mature retina.

Authors:  M Lahav; D M Albert; J L Craft
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1975

3.  [Congenital toxoplasmosis with atypical detachment and necrosis of the retina, persistence of the primary vitreous body, additional abnormalities and extensive intraocular ectopic hematopoiesis].

Authors:  B Gloor; R Haller
Journal:  Albrecht Von Graefes Arch Klin Exp Ophthalmol       Date:  1968

4.  In vitro model of retinal photoreceptor differentiation.

Authors:  M Lahav
Journal:  Trans Am Ophthalmol Soc       Date:  1987

5.  Dominantly inherited unilateral retinal dysplasia.

Authors:  I C Lloyd; A Colley; A B Tullo; R Bonshek
Journal:  Br J Ophthalmol       Date:  1993-06       Impact factor: 4.638

6.  Dominant exudative vitreoretinopathy and other vascular developmental disorders of the peripheral retina.

Authors:  C E van Nouhuys
Journal:  Doc Ophthalmol       Date:  1982-09-23       Impact factor: 2.379

7.  Non-oxygen induced retinitis proliferans and retinal detachment in full-term infants.

Authors:  F H Stefani; H Ehalt
Journal:  Br J Ophthalmol       Date:  1974-05       Impact factor: 4.638

8.  Unilateral sporadic retinal dysplasia: results of histopathologic, immunohistochemical, chromosomal, genetic, and VEGF-A analyses.

Authors:  Frederick A Jakobiec; Fouad R Zakka; Robert D'Amato; Margaret M Deangelis; David S Walton; Rajesh C Rao
Journal:  J AAPOS       Date:  2011-12       Impact factor: 1.220

9.  Retinal dysplasia.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-07-15       Impact factor: 2.379

10.  Probably Norrie's disease due to mutation. Two sporadic sibships of two males each, a necropsy of one case, and, given Norrie's disease, a calculation of the gene mutation frequency.

Authors:  C I Phillips; M Newton; J Duvall; S Holloway; A M Levy
Journal:  Br J Ophthalmol       Date:  1986-04       Impact factor: 4.638
  10 in total

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