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American Journal of Human Genetics|August 14, 2010
Nonsense mutations in FAM161A cause RP28-associated recessive retinitis pigmentosaThomas Langmann, Silvio Alessandro Di Gioia, Isabella Rau, et al.
Human Molecular Genetics|June 1, 1997
Mouse choroideremia gene mutation causes photoreceptor cell degeneration and is not transmitted through the female germlineJ A van den Hurk, W Hendriks, D J van de Pol, et al.
JAMA Ophthalmology|May 26, 2018
Olfactory Dysfunction in Patients With CNGB1-Associated Retinitis PigmentosaPeter Charbel Issa, Peggy Reuter, Laura Kühlewein, et al.
American Journal of Ophthalmology|June 12, 2018
Longitudinal Changes of Fixation Location and Stability Within 12 Months in Stargardt Disease: ProgStar Report No. 12Etienne M Schönbach, Rupert W Strauss, Xiangrong Kong, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|July 4, 2019
Full-field electroretinography, visual acuity and visual fields in Usher syndrome: a multicentre European studyKatarina Stingl, Anne Kurtenbach, Gesa Hahn, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 25, 2010
Restoration of useful vision up to letter recognition capabilities using subretinal microphotodiodesHeval Benav, Karl U Bartz-Schmidt, Dorothea Besch, et al.
Investigative Ophthalmology & Visual Science|May 8, 2012
Positioning of electronic subretinal implants in blind retinitis pigmentosa patients through multimodal assessment of retinal structuresAkos Kusnyerik, Udo Greppmaier, Robert Wilke, et al.
Plos One|November 14, 2014
Identification of a common non-apoptotic cell death mechanism in hereditary retinal degenerationBlanca Arango-Gonzalez, Dragana Trifunović, Ayse Sahaboglu, et al.
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