REFERENCES
- Stargardt K. Uber familiare, progressive degeneration in der makulagegend des auges. Albrecht Von Graefes Arch Ophthalmol 1909;71:534–550.
- Burke TR, Tsang SH. Allelic and phenotypic heterogeneity in ABCA4 mutations. Ophthalmic Genet 2011;32:165–174.
- Fishman GA. Fundus flavimaculatus. A clinical classification. Arch Ophthalmol 1976;94:2061–2067.
- Chen Y, Roorda A, Duncan JL. Advances in imaging of Stargardt disease. Adv Exp Med Biol 2010;664:333–340.
- Gomes NL, Greenstein VC, Carlson JN, et al. A comparison of fundus autofluorescence and retinal structure in patients with Stargardt disease. Invest Ophthalmol Vis Sci 2009;50:3953–3959.
- Lois N, Holder GE, Bunce C, et al. Phenotypic subtypes of Stargardt macular dystrophy-fundus flavimaculatus. Arch Ophthalmol 2001;119:359–369.
- Querques G, Prato R, Iaculli C, et al. Correlation of visual function impairment and OCT findings in patients with Stargardt disease and fundus flavimaculatus. Eur J Ophthalmol 2008;18:239–247.
- Wirtitsch MG, Ergun E, Hermann B, et al. Ultrahigh resolution optical coherence tomography in macular dystrophy. Am J Ophthalmol 2005;140:976–983.
- Zawadzki RJ, Jones SM, Olivier SS, et al. Adaptive-optics optical coherence tomography for high-resolution and high-speed 3D retinal in vivo imaging. Opt Express 2005;13:8532–8546.
- Cideciyan AV, Aleman TS, Swider M, et al. Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence. Hum Mol Genet 2004;13:525–534.
- Ergun E, Hermann B, Wirtitsch M, et al. Assessment of central visual function in Stargardt’s disease/fundus flavimaculatus with ultrahigh-resolution optical coherence tomography. Invest Ophthalmol Vis Sci 2005;46:310–316.
- Rodriguez-Marco NA, Andonegui-Navarro J, Compains-Silva E, et al. Optical coherence tomography and macular phototoxicity. Arch Soc Esp Oftalmol 2008;83:267–271.
- Fryczkowski P, Jedruch A, Kmera-Muszynska M. Spontaneous RPE tear in high myopia. Klin Oczna 2006;108:327–331.
- Marcus DM, Rustgi AK, Defoe D, et al. Retinal pigment epithelium abnormalities in mice with adenomatous polyposis coli gene disruption. Arch Ophthalmol 1997;115:645–650.