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Translational Vision Science & Technology|September 17, 2025
Stargardt's Connected Research Network Inaugural Meeting: Landscape Review and Horizon Scanning of Stargardt DiseaseAlexis Ceecee Britten-Jones, Saoud Al-Khuzaei, Matteo Rizzi, et al.
American Journal of Ophthalmology|August 25, 2022
Baseline Microperimetry and OCT in the RUSH2A Study: Structure-Function Association and Correlation With Disease SeverityEleonora M Lad, Jacque L Duncan, Wendi Liang, et al.
American Journal of Human Genetics|January 11, 2016
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2Alice E Davidson, Petra Liskova, Cerys J Evans, et al.
Investigative Ophthalmology & Visual Science|February 5, 2025
Characterizing the Genetic Basis for Inherited Retinal Disease: Lessons Learned From the Foundation Fighting Blindness Clinical Consortium's Gene PollKari Branham, Lassana Samarakoon, Isabelle Audo, et al.
American Journal of Human Genetics|January 31, 2012
X-linked megalocornea caused by mutations in CHRDL1 identifies an essential role for ventroptin in anterior segment developmentTom R Webb, Mar Matarin, Jessica C Gardner, et al.
Translational Vision Science & Technology|October 9, 2024
Endpoints and Design for Clinical Trials in USH2A-Related Retinal Degeneration: Results and Recommendations From the RUSH2A Natural History StudyMaureen G Maguire, David G Birch, Jacque L Duncan, et al.
JAMA|December 14, 2011
ADHD medications and risk of serious cardiovascular events in young and middle-aged adultsLaurel A Habel, William O Cooper, Colin M Sox, et al.
Pharmacoepidemiology and Drug Safety|September 15, 2020
Validity of diagnosis and procedure codes for identifying neural tube defects in infantsT Craig Cheetham, Sascha Dublin, Gaia Pocobelli, et al.
Molecular Cell|June 25, 2019
LINE-1 Evasion of Epigenetic Repression in HumansFrancisco J Sanchez-Luque, Marie-Jeanne H C Kempen, Patricia Gerdes, et al.
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