Analysis of Retinal Flecks in Fundus Flavimaculatus Using High-Definition Spectral-Domain Optical Coherence Tomography

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

F. P. M. Cremers · Human Molecular Genetics · 1998 · 552 citations

Adaptive-optics optical coherence tomography for high-resolution and high-speed 3D retinal in vivo imaging

Robert J. Zawadzki, Steven M. Jones, Scot S. Olivier et al. · Optics Express · 2005 · 429 citations · Full text

Vivo Imaging, Engineering, Microscopy +22

Phenotypic Subtypes of Stargardt Macular Dystrophy–Fundus Flavimaculatus

Noemi Lois · Archives of Ophthalmology · 2001 · 320 citations

High-Resolution Spectral Domain-OCT Imaging in Geographic Atrophy Associated with Age-Related Macular Degeneration

Monika Fleckenstein, Peter Charbel Issa, Hans‐Martin Helb et al. · Investigative Ophthalmology & Visual Science · 2008 · 281 citations

Mutations in ABCA4 result in accumulation of lipofuscin before slowing of the retinoid cycle: a reappraisal of the human disease sequence

Artur V. Cideciyan, Tomás S. Alemán, Małgorzata Świder et al. · Human Molecular Genetics · 2004 · 264 citations · Full text

Ocular Disease, Signal Transduction, Retinoid Cycle +14