Corneal endothelial dysfunction in Pearson syndrome-Reference-Cited by-同舟云学术

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Corneal endothelial dysfunction in Pearson syndrome

Published:2011-09-21 Issue:1-2 Volume:34 Page:55-57
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Kasbekar Shivani A.,Gonzalez-Martin Jose A.,Shafiq Ayad E.,Chandna Arvind,Willoughby Colin E.

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816810.2011.610862

Reference18 articles.

1. Kearns-Sayre's syndrome developing in a boy who survived Pearson's syndrome caused by mitochondrial DNA deletion

2. Pearson syndrome: Altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities

3. Fuchs' endothelial dystrophy of the cornea

4. Age-related changes of the corneal endothelium and stroma as seen in vivo by specular microscopy

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1. Inherited mitochondrial dysfunction triggered by OPA1 mutation impacts the sensory innervation fibre identity, functionality and regenerative potential in the cornea;Scientific Reports;2024-08-13

2. Inherited mitochondrial dysfunction triggered by OPA1 mutation impacts the sensory innervation fibre identity, functionality and regenerative potential in the cornea;2024-04-22

3. Mitochondria and Eye;Mutagenesis [Working Title];2021-03-15

4. Fuchs endothelial corneal dystrophy: The vicious cycle of Fuchs pathogenesis;Progress in Retinal and Eye Research;2021-01

5. Corneal Abnormalities Are Novel Clinical Feature in Wolfram Syndrome;American Journal of Ophthalmology;2020-09

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