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Molecular Vision|April 26, 2006
A large deletion in the adRP gene PRPF31: evidence that haploinsufficiency is the cause of diseaseLeen Abu-Safieh, Eranga N Vithana, Irmela Mantel, et al.Molecular Vision|November 23, 2013
Clinical characteristics of early retinal disease due to CDHR1 mutationRola Ba-Abbad, Panagiotis I Sergouniotis, Vincent Plagnol, et al.The British Journal of Ophthalmology|January 30, 2016
The ophthalmic presentation of Hermansky-Pudlak syndrome 6Sarah Hull, Gavin Arno, Graham E Holder, et al.Journal of Vision|March 6, 2008
The loss of the PDE6 deactivating enzyme, RGS9, results in precocious light adaptation at low light levelsAndrew Stockman, Hannah E Smithson, Andrew R Webster, et al.Retina (Philadelphia, Pa.)|March 12, 2011
Serial imaging and structure-function correlates of high-density rings of fundus autofluorescence in retinitis pigmentosaAnthony G Robson, Adnan Tufail, Fred Fitzke, et al.Acta Ophthalmologica|January 8, 2013
Phenotypic findings in C1QTNF5 retinopathy (late-onset retinal degeneration)Vasileios Soumplis, Panagiotis I Sergouniotis, Anthony G Robson, et al.Eye (London, England)|February 1, 2014
A detailed phenotypic description of autosomal dominant cone dystrophy due to a de novo mutation in the GUCY2D geneR Mukherjee, A G Robson, G E Holder, et al.Acta Ophthalmologica|October 20, 2011
A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 genePanagiotis I Sergouniotis, Anthony G Robson, Zheng Li, et al.Investigative Ophthalmology & Visual Science|August 18, 2012
Comparison of fundus autofluorescence with photopic and scotopic fine matrix mapping in patients with retinitis pigmentosa: 4- to 8-year follow-upAnthony G Robson, Eva Lenassi, Zubin Saihan, et al.Eye (London, England)|June 4, 2026
Robust and reproducible population receptive field mapping in patients with retinal pathologiesMaximilian Pawloff, David Linhardt, Michael Woletz, et al.Pageof 36