Reply Publication: Journal Article Lambert, Scott, Deborah VanderVeen, Vinay Aakalu, and Stephen Kim. 2020. “Reply”. Ophthalmology 127 (1): e8-e9.
Reply Publication: Journal Article Lambert, Scott, Deborah VanderVeen, and Stephen Kim. 2020. “Reply”. Ophthalmology 127 (1): e6-e7.
AAV-Mediated Gene Augmentation Therapy Restores Critical Functions in Mutant PRPF31 iPSC-Derived RPE Cells Publication: Journal Article Brydon, Elizabeth, Revital Bronstein, Adriana Buskin, Majlinda Lako, Eric Pierce, and Rosario Fernandez-Godino. 2019. “AAV-Mediated Gene Augmentation Therapy Restores Critical Functions in Mutant PRPF31 IPSC-Derived RPE Cells”. Mol Ther Methods Clin Dev 15: 392-402.
Loss of NQO1 generates genotoxic estrogen-DNA adducts in Fuchs Endothelial Corneal Dystrophy Publication: Journal Article Miyajima, Taiga, Geetha Melangath, Shan Zhu, Neha Deshpande, Shivakumar Vasanth, Bodhisattwa Mondal, Varun Kumar, et al. 2020. “Loss of NQO1 Generates Genotoxic Estrogen-DNA Adducts in Fuchs Endothelial Corneal Dystrophy”. Free Radic Biol Med 147: 69-79.
Evaluation and Management of V pattern Strabismus in Craniosynostosis Publication: Journal Article Elhusseiny, Abdelrahman, Elisah Huynh, and Linda Dagi. 2019. “Evaluation and Management of V Pattern Strabismus in Craniosynostosis”. J Binocul Vis Ocul Motil, 1-6.
Ultraviolet A light induces DNA damage and estrogen-DNA adducts in Fuchs endothelial corneal dystrophy causing females to be more affected Publication: Journal Article Liu, Cailing, Taiga Miyajima, Geetha Melangath, Takashi Miyai, Shivakumar Vasanth, Neha Deshpande, Varun Kumar, et al. 2020. “Ultraviolet A Light Induces DNA Damage and Estrogen-DNA Adducts in Fuchs Endothelial Corneal Dystrophy Causing Females to Be More Affected”. Proc Natl Acad Sci U S A 117 (1): 573-83.
Pediatric Idiopathic Intracranial Hypertension Publication: Journal Article Gaier, Eric, and Gena Heidary. 2019. “Pediatric Idiopathic Intracranial Hypertension”. Semin Neurol 39 (6): 704-10.
Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss Publication: Journal Article Gauthier, Angela, and Janey Wiggs. 2020. “Childhood Glaucoma Genes and Phenotypes: Focus on FOXC1 Mutations Causing Anterior Segment Dysgenesis and Hearing Loss”. Exp Eye Res 190: 107893.
A new patient-centered approach to ocular surface discomfort Publication: Journal Article Modjtahedi, Bobeck, Deborah Jacobs, and Donald Fong. 2020. “A New Patient-Centered Approach to Ocular Surface Discomfort”. Ocul Surf 18 (2): 196-98.
New observations and emerging ideas in diagnosis and management of non-infectious uveitis: A review Publication: Journal Article Rosenbaum, James, Bahram Bodaghi, Cristobal Couto, Manfred Zierhut, Nisha Acharya, Carlos Pavesio, Mei-Ling Tay-Kearney, et al. 2019. “New Observations and Emerging Ideas in Diagnosis and Management of Non-Infectious Uveitis: A Review”. Semin Arthritis Rheum 49 (3): 438-45.