Literature DB >> 29270096

A 48-year-old man presents with bilateral corneal deposits.

Shaminder S Bhullar1, Gerami D Seitzman1.   

Abstract

Entities:  

Year:  2009        PMID： 29270096      PMCID： PMC5734906          DOI： 10.5693/djo.03.2009.009

Source DB:  PubMed          Journal:  Digit J Ophthalmol        ISSN： 1542-8958


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  5 in total

1.  De novo mutation in the BIGH3/TGFB1 gene causing granular corneal dystrophy.

Authors:  E N Hilton; G C M Black; F D C Manson; D F Schorderet; F L Munier
Journal:  Br J Ophthalmol       Date:  2007-08       Impact factor: 4.638

2.  Mutation hot spots in 5q31-linked corneal dystrophies.

Authors:  E Korvatska; F L Munier; A Djemaï; M X Wang; B Frueh; A G Chiou; S Uffer; E Ballestrazzi; R E Braunstein; R K Forster; W W Culbertson; H Boman; L Zografos; D F Schorderet
Journal:  Am J Hum Genet       Date:  1998-02       Impact factor: 11.025

3.  Phenotypic non-penetrance in granular corneal dystrophy type II.

Authors:  Jung-Wan Kim; Hyo-Myung Kim; Jong-Suk Song
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2008-05-06       Impact factor: 3.117

4.  An unusual clinical phenotype of Avellino corneal dystrophy associated with an Arg124His beta iG-H3 mutation in an African-American woman.

Authors:  Mario A Meallet; John A Affeldt; Trevor J McFarland; Binoy Appukuttan; Rusell Read; J Timothy Stout; Narsing A Rao
Journal:  Am J Ophthalmol       Date:  2004-04       Impact factor: 5.258

5.  Deep anterior lamellar keratoplasty with melles technique for granular corneal dystrophy.

Authors:  Ramin Salouti; Hamid Hosseini; Masoomeh Eghtedari; Mohammad R Khalili
Journal:  Cornea       Date:  2009-02       Impact factor: 2.651
  5 in total

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