Clinical classification of Stargardt disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Link
https://link.springer.com/content/pdf/10.1007/s00417-023-06292-x.pdf
Reference5 articles.
1. Kim LS, Fishman GA (2006) Comparison of visual acuity loss in patients with different stages of Stargardt's disease. Ophthalmology 113:1748–1751. https://doi.org/10.1016/j.ophtha.2006.04.027
2. van Driel MA, Maugeri A, Klevering BJ, Hoyng CB, Cremers FPM (1998) ABCR unites what ophthalmologists divide(s). Ophthalmic Genetics 19:117–122. https://doi.org/10.1076/opge.19.3.117.2187
3. Lois N, Holder GE, Bunce C, Fitzke FW, Bird AC (2001) Phenotypic subtypes of stargardt macular dystrophy. Arch Ophthalmol:359–369
4. Lambertus S, van Huet RA, Bax NM, Hoefsloot LH, Cremers FP, Boon CJ, Klevering BJ, Hoyng CB (2015) Early-onset stargardt disease: phenotypic and genotypic characteristics. Ophthalmology 122:335–344. https://doi.org/10.1016/j.ophtha.2014.08.032
5. Li CHZ, Pas J, Corradi Z, Hitti-Malin RJ, Hoogstede A, Runhart EH, Dhooge PPA, Collin RWJ, Cremers FPM, Hoyng CB (2023) Study of late-onset Stargardt type 1 disease: characteristics, genetics and progression. Ophthalmology. https://doi.org/10.1016/j.ophtha.2023.08.011
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