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American Journal of Ophthalmology Case Reports
|
August 9, 2021
Syphilitic interstitial keratitis treated with topical tacrolimus
Jacob Martin, Laura Kopplin, Deborah Costakos
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
July 24, 2012
Bilateral central retinal artery occlusions in an infant with hyperhomocysteinemia
Peter Karth, Ravi Singh, Judy Kim, et al.
Progress in Retinal and Eye Research
|
August 3, 2024
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms
Linda M Reis, Sarah E Seese, Deborah Costakos, et al.
BMC Medical Genetics
|
September 10, 2016
Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
Hannah Happ, Eric Weh, Deborah Costakos, et al.
Clinical Genetics
|
December 14, 2020
Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia
Linda M Reis, Deborah Costakos, Patricia G Wheeler, et al.
Human Genetics
|
March 20, 2013
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes
Linda M Reis, Rebecca C Tyler, Sanaa Muheisen, et al.
Investigative Ophthalmology & Visual Science
|
March 5, 2024
Quantitative Foveal Structural Metrics as Predictors of Visual Acuity in Human Albinism
Erica N Woertz, Gelique D Ayala, Niamh Wynne, et al.
Molecular Vision
|
October 26, 2016
Analysis of <i>CYP1B1</i> in pediatric and adult glaucoma and other ocular phenotypes
Linda M Reis, Rebecca C Tyler, Eric Weh, et al.
Translational Vision Science & Technology
|
June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure
Katie M Litts, Erica N Woertz, Niamh Wynne, et al.
European Journal of Human Genetics : EJHG
|
April 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlations
Solomon S Merepa, Linda M Reis, Alejandra Damián, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
American Journal of Ophthalmology Case Reports
|
August 9, 2021
Syphilitic interstitial keratitis treated with topical tacrolimus
Jacob Martin, Laura Kopplin, Deborah Costakos
Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus
|
July 24, 2012
Bilateral central retinal artery occlusions in an infant with hyperhomocysteinemia
Peter Karth, Ravi Singh, Judy Kim, et al.
Progress in Retinal and Eye Research
|
August 3, 2024
Congenital anterior segment ocular disorders: Genotype-phenotype correlations and emerging novel mechanisms
Linda M Reis, Sarah E Seese, Deborah Costakos, et al.
BMC Medical Genetics
|
September 10, 2016
Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract
Hannah Happ, Eric Weh, Deborah Costakos, et al.
Clinical Genetics
|
December 14, 2020
Dominant variants in PRR12 result in unilateral or bilateral complex microphthalmia
Linda M Reis, Deborah Costakos, Patricia G Wheeler, et al.
Human Genetics
|
March 20, 2013
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes
Linda M Reis, Rebecca C Tyler, Sanaa Muheisen, et al.
Investigative Ophthalmology & Visual Science
|
March 5, 2024
Quantitative Foveal Structural Metrics as Predictors of Visual Acuity in Human Albinism
Erica N Woertz, Gelique D Ayala, Niamh Wynne, et al.
Molecular Vision
|
October 26, 2016
Analysis of <i>CYP1B1</i> in pediatric and adult glaucoma and other ocular phenotypes
Linda M Reis, Rebecca C Tyler, Eric Weh, et al.
Translational Vision Science & Technology
|
June 10, 2021
Examining Whether AOSLO-Based Foveal Cone Metrics in Achromatopsia and Albinism Are Representative of Foveal Cone Structure
Katie M Litts, Erica N Woertz, Niamh Wynne, et al.
European Journal of Human Genetics : EJHG
|
April 29, 2025
GJA8-associated developmental eye disorders: a new multicentre study highlights mutational hotspots and genotype-phenotype correlations
Solomon S Merepa, Linda M Reis, Alejandra Damián, et al.
Page
of 2