Choroidal vascularity index in hereditary optic neuropathies
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
https://www.nature.com/articles/s41433-023-02383-5.pdf
Reference33 articles.
1. Theodorou-Kanakari A, Karampitianis S, Karageorgou V, Kampourelli E, Kapasakis E, Theodossiadis P, et al. Current and emerging treatment modalities for Leber’s hereditary optic neuropathy: A review of the literature. Adv Ther. 2018;35:1510–8.
2. Yu-Wai-Man P, Griffiths PG, Brown DT, Howell N, Turnbull DM, Chinnery PF. The epidemiology of Leber hereditary optic neuropathy in the North East of England. Am J Hum Genet. 2003;72:333–9. Erratum in: Am J Hum Genet. 2016;98:1271.
3. Wallace DC, Singh G, Lott MT, Hodge JA, Schurr TG, Lezza AM, et al. Mitochondrial DNA mutation associated with Leber’s hereditary optic neuropathy. Science. 1988;242:1427–30.
4. Yu-Wai-Man P, Griffiths PG, Burke A, Sellar PW, Clarke MP, Gnanaraj L, et al. The prevalence and natural history of dominant optic atrophy due to OPA1 mutations. Ophthalmology. 2010;117:1538–46.
5. Moster SJ, Moster ML, Bryan MS, Sergott RC. Retinal ganglion cell and inner plexiform layer loss correlate with visual acuity loss in LHON: A longitudinal, segmentation OCT analysis. Investig Ophthalmol Vis Sci. 2016. https://doi.org/10.1167/iovs.15-17328.
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1. Factors affecting choroidal circulation parameters in 4–14-year-old Chinese children measured by SS-OCT/OCTA;Photodiagnosis and Photodynamic Therapy;2024-08
2. Choriocapillaris and choroidal thickness in all Leber hereditary optic neuropathy stages using swept source technology;Acta Ophthalmologica;2023-11-20
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