Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options

Por Tanna, Preena, Strauss, Rupert W, Fujinami, Kaoru, Michaelides, Michel
Publicado no Br J Ophthalmol (2017)

Assessment of estimated retinal atrophy progression in Stargardt macular dystrophy using spectral-domain optical coherence tomography

Por Strauss, Rupert W, Muñoz, Beatriz, Wolfson, Yulia, Sophie, Raafay, Fletcher, Emily, Bittencourt, Millena G, Scholl, Hendrik P N
Publicado no Br J Ophthalmol (2016)

Cross-Sectional and Longitudinal Assessment of Retinal Sensitivity in Patients With Childhood-Onset Stargardt Disease

Por Tanna, Preena, Georgiou, Michalis, Aboshiha, Jonathan, Strauss, Rupert W., Kumaran, Neruban, Kalitzeos, Angelos, Weleber, Richard G., Michaelides, Michel
Publicado no Transl Vis Sci Technol (2018)

Is There Excess Oxidative Stress and Damage in Eyes of Patients with Retinitis Pigmentosa?

Por Campochiaro, Peter A., Strauss, Rupert W., Lu, Lili, Hafiz, Gulnar, Wolfson, Yulia, Shah, Syed M., Sophie, Raafay, Mir, Tahreem A., Scholl, Hendrik P.
Publicado no Antioxid Redox Signal (2015)

Retinal Architecture in ​RGS9- and ​R9AP-Associated Retinal Dysfunction (Bradyopsia)

Por Strauss, Rupert W., Dubis, Adam M., Cooper, Robert F., Ba-Abbad, Rola, Moore, Anthony T., Webster, Andrew R., Dubra, Alfredo, Carroll, Joseph, Michaelides, Michel
Publicado no Am J Ophthalmol (2015)

Unilateral BEST1-Associated Retinopathy

Por Arora, Rashi, Khan, Kamron, Kasilian, Melissa L., Strauss, Rupert W., Holder, Graham E., Robson, Anthony G., Thompson, Dorothy A., Moore, Anthony T., Michaelides, Michel
Publicado no Am J Ophthalmol (2016)

Comparison of Short-Wavelength Reduced-Illuminance and Conventional Autofluorescence Imaging in Stargardt Macular Dystrophy

Por Strauss, Rupert W., Muñoz, Beatriz, Jha, Anamika, Ho, Alexander, Cideciyan, Artur V., Kasilian, Melissa L., Wolfson, Yulia, Sadda, SriniVas, West, Sheila, Scholl, Hendrik P.N., Michaelides, Michel
Publicado no Am J Ophthalmol (2016)

Visual Acuity Change Over 24 Months and Its Association With Foveal Phenotype and Genotype in Individuals With Stargardt Disease: ProgStar Study Report No. 10

Por Kong, Xiangrong, Fujinami, Kaoru, Strauss, Rupert W., Munoz, Beatriz, West, Sheila K., Cideciyan, Artur V., Michaelides, Michel, Ahmed, Mohamed, Ervin, Ann-Margret, Schönbach, Etienne, Cheetham, Janet K., Scholl, Hendrik P. N.
Publicado no JAMA Ophthalmol (2018)

Incidence of Atrophic Lesions in Stargardt Disease in the Progression of Atrophy Secondary to Stargardt Disease (ProgStar) Study: Report No. 5

Por Strauss, Rupert W., Muñoz, Beatriz, Ho, Alex, Jha, Anamika, Michaelides, Michel, Mohand-Said, Saddek, Cideciyan, Artur V., Birch, David, Hariri, Amir H., Nittala, Muneeswar G., Sadda, SriniVas, Scholl, Hendrik P. N.
Publicado no JAMA Ophthalmol (2017)

Progression of Stargardt Disease as Determined by Fundus Autofluorescence in the Retrospective Progression of Stargardt Disease Study (ProgStar Report No. 9)

Por Strauss, Rupert W., Muñoz, Beatriz, Ho, Alexander, Jha, Anamika, Michaelides, Michel, Cideciyan, Artur V., Audo, Isabelle, Birch, David G., Hariri, Amir H., Nittala, Muneeswar G., Sadda, SriniVas, West, Sheila, Scholl, Hendrik P. N.
Publicado no JAMA Ophthalmol (2017)