Accelerated Accumulation of Lipofuscin Pigments in the RPE of a Mouse Model for ABCA4-Mediated Retinal Dystrophies following Vitamin A Supplementation
Radu, Roxana A., Yuan, Quan, Hu, Jane, Peng, Jennifer H., Lloyd, Marcia, Nusinowitz, Steven, Bok, Dean, Travis, Gabriel H.·2008·Investigative Opthalmology & Visual Science
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- Morbus Stargardt: Genetik, molekulare Mechanismen, mögliche Lebensstilinterventionen und PharmakotherapieTheresa Lipsky, Sophia Dithmar, Georg Ansari, Virginie Peter, Hanno J. Bolz, Tobias Duncker, Monika Fleckenstein, Peter Charbel Issa, Christina Gerth‐Kahlert, Moreno Menghini et al. · 2026 · Die Ophthalmologie
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- The value of genetic testing for inherited retinal disease caused by mutations in the ABCA4 gene in South AfricansLisa J. Roberts, Stephni Hardie, Taahira Goolam Hoosen, Raj Ramesar, Leslie S. Greenberg · 2013 · South African Medical Journal
- Gene Therapy, Diet and Drug Approaches to Treating Inherited Retinal DiseaseMatthew P. Simunovic, Heather Gwen Mack, Lauren N. Ayton, Mark Hassall · 2021 · Elsevier eBooks
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- Genetic Etiology and Clinical Consequences of Cone DisordersAlberta A. H. J. Thiadens · 2011 · RePub (Erasmus University Rotterdam)
- Recherche de gènes impliqués dans des rétinopathies canines comme modèles de rétinites pigmentaires humainesMorgane Bunel · 2017
- Characterization of RPE65 and RDH12, two enzymes associated with retinal dystrophy and retinoid processingJared D. Chrispell · 2010 · Deep Blue (University of Michigan)
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- Genetics of inherited retinal degenerationEmily I. Schindler · 2011
- Primary Photoreceptor Degenerations: TerminologyMark Edward Pennesi, Peter James Francis, Richard G. Weleber · 2010 · Elsevier eBooks
- Retinoic Acid Receptor Beta in Pathophysiology of Age-Related Macular Degeneration.Tavakolifar Saeed, Sina Lasemi, Sajad Mohammadgholiha, Zahra‐Soheila Soheili · 2015 · Europe PMC (PubMed Central)
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- LETTER TO THE EDITOR: RETINOIC ACID RECEPTOR BETA IN PATHOPHYSIOLOGY OF AGE-RELATED MACULAR DEGENERATIONTavakolifar Saeed, Sina Lasemi, Sajad Mohammadgholiha, Soheili Zahra Soheila · 2015
- called 'Quick 7' (which provides a genetic diagnosis, i.e. identification of both mutations, in 40% of Afrikaner patients with STGDLisa J. Roberts, Shannon L. Hardie, Taahira Goolam Hoosen, Raj Ramesar, Leslie S. Greenberg · 2013
- Macular disease genetics and supplementation: the evidence for choosing wiselyAndrea Louise Vincent, Alex P. Hunyor · 2016 · Clinical and Experimental Ophthalmology
- Effectiveness of new techniques of intraocular stem cells transplantation in the treatment of retinitis pigmentosaВ М Шелудченко, Maria V. Budzinskaya, И А Ронзина, Smirnova Tv · 2019 · Russian Annals of Ophthalmology
- Animal and Human Models of Retinal DiseasesErica Lucy Fletcher, Alice Pébay, Matt Rutar, Kiana Kakavand, Anna Y. Wang, Kirstan A. Vessey, Andrew Ian Jobling, Ursula Greferath · 2020 · Elsevier eBooks
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- Update on the Management of ABCA4 Retinopathy (Stargardt Disease)Deepika C. Parameswarappa, Dhanashree Ratra, Goura Chattannavar, Srikanta Kumar Padhy · 2026 · Ophthalmology and Therapy
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