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Human Molecular Genetics
|
October 4, 2017
A mutation in IFT43 causes non-syndromic recessive retinal degeneration
Pooja Biswas, Jacque L Duncan, Muhammad Ali, et al.
Investigative Ophthalmology & Visual Science
|
August 12, 2025
Progression of Dark-Adapted Visual Fields Over 3 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) Study
David G Birch, Jacque L Duncan, Lassana Samarakoon, et al.
Experimental Eye Research
|
November 11, 2017
Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration
Matthew M LaVail, Shimpei Nishikawa, Roy H Steinberg, et al.
Molecular Vision
|
December 10, 2013
Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa
Sara J Bowne, Lori S Sullivan, Cheryl E Avery, et al.
Experimental Eye Research
|
March 24, 2025
Assessing structure - Function relationships in non-neovascular age-related macular degeneration
Emily Y Chew, Catherine Cukras, Jacque L Duncan, et al.
Clinical & Experimental Optometry
|
August 26, 2016
Improvements in vision-related quality of life in blind patients implanted with the Argus II Epiretinal Prosthesis
Jacque L Duncan, Thomas P Richards, Aries Arditi, et al.
Investigative Ophthalmology & Visual Science
|
December 7, 2007
Intraocular CNTF reduces vision in normal rats in a dose-dependent manner
Trevor J McGill, Glen T Prusky, Robert M Douglas, et al.
Clinical & Experimental Ophthalmology
|
August 7, 2016
Performance of real-world functional vision tasks by blind subjects improves after implantation with the Argus® II retinal prosthesis system
Gislin Dagnelie, Punita Christopher, Aries Arditi, et al.
Journal of Medical Genetics
|
May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population
Gail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Experimental Eye Research
|
May 17, 2002
Macular pigment and lutein supplementation in choroideremia
Jacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Page
of 17
Search research articles
Search
Showing results (121-130 of 170) with videos related to
Sort By:
Page
of 17
Human Molecular Genetics
|
October 4, 2017
A mutation in IFT43 causes non-syndromic recessive retinal degeneration
Pooja Biswas, Jacque L Duncan, Muhammad Ali, et al.
Investigative Ophthalmology & Visual Science
|
August 12, 2025
Progression of Dark-Adapted Visual Fields Over 3 Years in the Rate of Progression in USH2A-Related Retinal Degeneration (RUSH2A) Study
David G Birch, Jacque L Duncan, Lassana Samarakoon, et al.
Experimental Eye Research
|
November 11, 2017
Phenotypic characterization of P23H and S334ter rhodopsin transgenic rat models of inherited retinal degeneration
Matthew M LaVail, Shimpei Nishikawa, Roy H Steinberg, et al.
Molecular Vision
|
December 10, 2013
Mutations in the small nuclear riboprotein 200 kDa gene (SNRNP200) cause 1.6% of autosomal dominant retinitis pigmentosa
Sara J Bowne, Lori S Sullivan, Cheryl E Avery, et al.
Experimental Eye Research
|
March 24, 2025
Assessing structure - Function relationships in non-neovascular age-related macular degeneration
Emily Y Chew, Catherine Cukras, Jacque L Duncan, et al.
Clinical & Experimental Optometry
|
August 26, 2016
Improvements in vision-related quality of life in blind patients implanted with the Argus II Epiretinal Prosthesis
Jacque L Duncan, Thomas P Richards, Aries Arditi, et al.
Investigative Ophthalmology & Visual Science
|
December 7, 2007
Intraocular CNTF reduces vision in normal rats in a dose-dependent manner
Trevor J McGill, Glen T Prusky, Robert M Douglas, et al.
Clinical & Experimental Ophthalmology
|
August 7, 2016
Performance of real-world functional vision tasks by blind subjects improves after implantation with the Argus® II retinal prosthesis system
Gislin Dagnelie, Punita Christopher, Aries Arditi, et al.
Journal of Medical Genetics
|
May 18, 2010
Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population
Gail Billingsley, Jenea Bin, Karen J Fieggen, et al.
Experimental Eye Research
|
May 17, 2002
Macular pigment and lutein supplementation in choroideremia
Jacque L Duncan, Tomas S Aleman, Leigh M Gardner, et al.
Page
of 17