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Molecular Vision|November 9, 2011
RDH12 retinopathy: novel mutations and phenotypic descriptionDonna S Mackay, Arundhati Dev Borman, Phillip Moradi, et al.
Investigative Ophthalmology & Visual Science|May 10, 2012
Early onset retinal dystrophy due to mutations in LRAT: molecular analysis and detailed phenotypic studyArundhati Dev Borman, Louise A Ocaka, Donna S Mackay, et al.
Progress in Retinal and Eye Research|March 16, 2025
Gene Therapy-Associated Uveitis (GTAU): Understanding and mitigating the adverse immune response in retinal gene therapyRyan Purdy, Molly John, Alissa Bray, et al.
American Journal of Ophthalmology|August 29, 2024
Optic Nerve Head Morphological Variation in Craniosynostosis: A Cohort StudySohaib R Rufai, Mervyn G Thomas, Oliver R Marmoy, et al.
Human Mutation|October 3, 2017
Missense variants in the X-linked gene PRPS1 cause retinal degeneration in femalesAlessia Fiorentino, Kaoru Fujinami, Gavin Arno, et al.
American Journal of Ophthalmology|May 12, 2023
First-in-Human Gene Therapy Trial of AAV8-hCARp.hCNGB3 in Adults and Children With CNGB3-associated AchromatopsiaMichel Michaelides, Nashila Hirji, Sui Chien Wong, et al.
Human Mutation|November 30, 2020
New variants and in silico analyses in GRK1 associated Oguchi diseaseJames A Poulter, Molly S C Gravett, Rachel L Taylor, et al.
Ophthalmology. Retina|November 25, 2020
Traumatic Retinal Detachment in Patients with Self-Injurious Behavior: An International Multicenter StudyElizabeth J Rossin, Irena Tsui, Sui Chien Wong, et al.
Ophthalmology|May 26, 2016
Immediate Sequential Bilateral Pediatric Vitreoretinal Surgery: An International Multicenter StudyYoshihiro Yonekawa, Wei-Chi Wu, Shunji Kusaka, et al.
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