Assessment of corneal topographic, tomographic, densitometric, and biomechanical properties of Fabry patients with ocular manifestations-Reference-Cited by-同舟云学术

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Assessment of corneal topographic, tomographic, densitometric, and biomechanical properties of Fabry patients with ocular manifestations

Published:2020-01-08 Issue:5 Volume:258 Page:1057-1064
ISSN:0721-832X
Container-title:Graefe's Archive for Clinical and Experimental Ophthalmology
language:en
Short-container-title:Graefes Arch Clin Exp Ophthalmol

Author:

Cankurtaran Veysel,Tekin Kemal,Cakmak Ayse Idil,Inanc Merve,Turgut Faruk Hilmi

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Link

http://link.springer.com/content/pdf/10.1007/s00417-019-04593-8.pdf

Reference38 articles.

1. Germain DP (2010) Fabry disease. Orphanet J Rare Dis 5:30

2. Poorthuis BJ, Wevers RA, Kleijer WJ, Groener JE, de Jong JG, van Weely S et al (1999) The frequency of lysosomal storage diseases in the Netherlands. Hum Genet 105:151–156

3. Spada M, Pagliardini S, Yasuda M, Tukel T, Thiagarajan G, Sakuraba H et al (2006) High incidence of later onset Fabry disease revealed by newborn screening. Am J Hum Genet 79:31–40

4. San Roman I, Rodriguez ME, Caporossi O, Zoppetti C, Sodi A, Mecocci A et al (2017) Computer assisted retinal vessel tortuosity evaluation in novel mutation Fabry disease: towards new prognostic markers. Retina 37:592–603

5. Sodi A, Ioannidis AS, Mehta A, Davey C, Beck M, Pitz S (2007) Ocular manifestations of Fabry’s disease: data from the Fabry Outcome Survey. Br J Ophthalmol 91:210–214

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