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The British Journal of Ophthalmology
|
November 27, 2020
Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophy
Razek G Coussa, Elaine M Binkley, Mark E Wilkinson, et al.
American Journal of Ophthalmology
|
March 21, 2007
Familial cavitary optic disk anomalies: identification of a novel genetic locus
John H Fingert, Robert A Honkanen, Suma P Shankar, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 2016
Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular Degeneration
Allison E Songstad, Luke A Wiley, Khahn Duong, et al.
The Journal of Clinical Investigation
|
August 9, 2011
Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma
Gulab S Zode, Markus H Kuehn, Darryl Y Nishimura, et al.
JAMA Ophthalmology
|
December 19, 2014
Comparison of retinal and choriocapillaris thicknesses following sitting to supine transition in healthy individuals and patients with age-related macular degeneration
David R P Almeida, Li Zhang, Eric K Chin, et al.
Ophthalmic Genetics
|
February 22, 2014
Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR Locus
Jonathan H Tzu, Tania Arguello, Audina M Berrocal, et al.
Investigative Ophthalmology & Visual Science
|
October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial Transcriptomics
Andrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Investigative Ophthalmology & Visual Science
|
December 6, 2024
Elevation of Granulocyte Colony Stimulating Factor in Human AMD Donor RPE-Choroid
Kelly Mulfaul, Adnan H Khan, Samantha G Schwarte, et al.
JAMA Ophthalmology
|
August 17, 2023
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery
Erin A Boese, Arlene V Drack, Benjamin R Roos, et al.
Human Molecular Genetics
|
July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
Samuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Page
of 39
Search research articles
Search
Showing results (271-280 of 384) with videos related to
Sort By:
Page
of 39
The British Journal of Ophthalmology
|
November 27, 2020
Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophy
Razek G Coussa, Elaine M Binkley, Mark E Wilkinson, et al.
American Journal of Ophthalmology
|
March 21, 2007
Familial cavitary optic disk anomalies: identification of a novel genetic locus
John H Fingert, Robert A Honkanen, Suma P Shankar, et al.
Investigative Ophthalmology & Visual Science
|
January 1, 2016
Generating iPSC-Derived Choroidal Endothelial Cells to Study Age-Related Macular Degeneration
Allison E Songstad, Luke A Wiley, Khahn Duong, et al.
The Journal of Clinical Investigation
|
August 9, 2011
Reduction of ER stress via a chemical chaperone prevents disease phenotypes in a mouse model of primary open angle glaucoma
Gulab S Zode, Markus H Kuehn, Darryl Y Nishimura, et al.
JAMA Ophthalmology
|
December 19, 2014
Comparison of retinal and choriocapillaris thicknesses following sitting to supine transition in healthy individuals and patients with age-related macular degeneration
David R P Almeida, Li Zhang, Eric K Chin, et al.
Ophthalmic Genetics
|
February 22, 2014
Clinical and Electrophysiologic Characteristics of a Large Kindred with X-Linked Retinitis Pigmentosa Associated with the RPGR Locus
Jonathan H Tzu, Tania Arguello, Audina M Berrocal, et al.
Investigative Ophthalmology & Visual Science
|
October 25, 2023
Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial Transcriptomics
Andrew P Voigt, Nathaniel K Mullin, Emma M Navratil, et al.
Investigative Ophthalmology & Visual Science
|
December 6, 2024
Elevation of Granulocyte Colony Stimulating Factor in Human AMD Donor RPE-Choroid
Kelly Mulfaul, Adnan H Khan, Samantha G Schwarte, et al.
JAMA Ophthalmology
|
August 17, 2023
GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery
Erin A Boese, Arlene V Drack, Benjamin R Roos, et al.
Human Molecular Genetics
|
July 2, 2004
Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration
Samuel G Jacobson, Alexander Sumaroka, Tomas S Aleman, et al.
Page
of 39