Literature DB >> 2698359

Duke-Elder lecture. Prevention and perspective in retinal detachment.

J D Scott1.   

Abstract

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Year:  1989        PMID： 2698359     DOI： 10.1038/eye.1989.82

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN： 0950-222X            Impact factor:   3.775


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  11 in total

1.  Vitreous phenotype: genotype correlation in Stickler syndrome.

Authors:  David McLeod; Graeme C M Black; Paul N Bishop
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2002-01       Impact factor: 3.117

2.  Autosomal dominant rhegmatogenous retinal detachment--clinical appearance and surgical outcome.

Authors:  Thomas Theelen; Sioe Lie Go; Maurits A D Tilanus; B Jeroen Klevering; August F Deutman; Frans P M Cremers; Carel B Hoyng
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2004-04-02       Impact factor: 3.117

Review 3.  Subretinal membranes of proliferative vitreoretinopathy.

Authors:  P Hiscott; I Grierson
Journal:  Br J Ophthalmol       Date:  1991-01       Impact factor: 4.638

4.  The pseudo-posterior limiting layer syndrome: a vitreoretinal heredodegeneration with autosomal dominant transmission. Graefe's Arch Clin Exp Ophthalmol (1994) 232:16-24.

Authors:  M P Snead; D K Newmann; A Poulson; J D Scott
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  1995-12       Impact factor: 3.117

Review 5.  Clinical and Molecular genetics of Stickler syndrome.

Authors:  M P Snead; J R Yates
Journal:  J Med Genet       Date:  1999-05       Impact factor: 6.318

Review 6.  Stickler syndrome, ocular-only variants and a key diagnostic role for the ophthalmologist.

Authors:  M P Snead; A M McNinch; A V Poulson; P Bearcroft; B Silverman; P Gomersall; V Parfect; A J Richards
Journal:  Eye (Lond)       Date:  2011-09-16       Impact factor: 3.775

Review 7.  Proliferative vitreoretinopathy.

Authors:  P K Leaver
Journal:  Br J Ophthalmol       Date:  1995-10       Impact factor: 4.638

8.  COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromes.

Authors:  A J Richards; S Martin; J R Yates; J D Scott; D M Baguley; F M Pope; M P Snead
Journal:  Br J Ophthalmol       Date:  2000-04       Impact factor: 4.638

9.  Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix.

Authors:  A J Richards; D M Baguley; J R Yates; C Lane; M Nicol; P S Harper; J D Scott; M P Snead
Journal:  Am J Hum Genet       Date:  2000-09-25       Impact factor: 11.025

10.  Mutation in collagen II alpha 1 isoforms delineates Stickler and Wagner syndrome phenotypes.

Authors:  Khanh-Nhat Tran-Viet; Vincent Soler; Valencia Quiette; Caldwell Powell; Tammy Yanovitch; Ravikanth Metlapally; Xiaoyan Luo; Nicholas Katsanis; Erica Nading; Terri L Young
Journal:  Mol Vis       Date:  2013-04-05       Impact factor: 2.367
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