Literature DB >> 14026621

Inherited retinal detachment.

W V DELANEY, W PODEDWORNY, W H HAVENER.   

Abstract

Entities:  

Keywords:  RETINAL DETACHMENT

Mesh：

Year:  1963        PMID： 14026621     DOI： 10.1001/archopht.1963.00960040050010

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


× No keyword cloud information.
  10 in total

1.  Stickler's syndrome and neovascular glaucoma.

Authors:  N J Young; R A Hitchings; K Sehmi; A C Bird
Journal:  Br J Ophthalmol       Date:  1979-12       Impact factor: 4.638

2.  Exclusion of COL2A1 as a candidate gene in a family with Wagner-Stickler syndrome.

Authors:  A E Fryer; M Upadhyaya; M Littler; P Bacon; D Watkins; P Tsipouras; P S Harper
Journal:  J Med Genet       Date:  1990-02       Impact factor: 6.318

3.  Wagner's syndrome.

Authors:  A Pinckers; L M Jansen
Journal:  Doc Ophthalmol       Date:  1974-11       Impact factor: 2.379

4.  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

Review 5.  The Wagner-Stickler syndrome complex.

Authors:  V Godel; P Nemet; M Lazar
Journal:  Doc Ophthalmol       Date:  1981-12-16       Impact factor: 2.379

6.  The Wagner syndrome versus hereditary arthroophthalmopathy.

Authors:  I H Maumenee; H U Stoll; M B Mets
Journal:  Trans Am Ophthalmol Soc       Date:  1982

7.  Syndromes of genetic juvenile retinal detachment.

Authors:  R J Gorlin; W H Knobloch
Journal:  Z Kinderheilkd       Date:  1972

8.  Retinal detachment in median cleft-face syndrome.

Authors:  V Feiler-Ofry; V Godel; P Nemet; M Lazar
Journal:  Br J Ophthalmol       Date:  1980-02       Impact factor: 4.638

9.  Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)

Authors:  J Körkkö; P Ritvaniemi; L Haataja; H Kääriäinen; K I Kivirikko; D J Prockop; L Ala-Kokko
Journal:  Am J Hum Genet       Date:  1993-07       Impact factor: 11.025

10.  Chorioretinal dysplasia in young subjects with Wagner's hereditary vitreoretinal degeneration.

Authors:  C E Van Nouhuys
Journal:  Int Ophthalmol       Date:  1981-03       Impact factor: 2.031
  10 in total

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