Showing results (71-80 of 213) with videos related to
Sort By:
Pageof 22
Journal of Neurosurgery|January 1, 2003
Treatment of an anterior communicating artery aneurysm through an anomalous anastomosis from the cavernous internal carotid arteryVirany Huynh Hillard, Kiran Musunuru, Chiedozie Nwagwu, et al.Cureus|February 22, 2024
An Adolescent Boy With Hypoxia, Microscopic Hematuria, and HypertensionMelissa S Zhou, Clement D Lee, Benjamin J Lerman, et al.Annals of Neurology|July 22, 2014
Targeted treatment of migrating partial seizures of infancy with quinidineDavid Bearden, Alanna Strong, Jessica Ehnot, et al.Seminars in Ophthalmology|April 22, 2024
Punctal Atresia As a Clinical Indicator of Systemic Genetic AnomaliesDaphna Landau-Prat, Rayna Marshall, Alanna Strong, et al.European Heart Journal|July 2, 2025
Gene therapy and genome editing for lipoprotein disordersChen Gurevitz, Archna Bajaj, Amit V Khera, et al.American Journal of Human Genetics|November 4, 2023
Efficient in vivo prime editing corrects the most frequent phenylketonuria variant, associated with high unmet medical needDominique L Brooks, Madelynn N Whittaker, Ping Qu, et al.Ophthalmic Plastic and Reconstructive Surgery|December 26, 2024
Ocular and Systemic Abnormalities in Punctal AgenesisRayna F Marshall, Daphna Landau-Prat, Alanna Strong, et al.Journal of Crohn'S & Colitis|February 17, 2025
The ulcerative colitis risk gene adenylyl cyclase 7 restrains the T-helper 2 phenotype and Class II antigen presentationChristopher J Cardinale, Yichuan Liu, Aayush Kevadia, et al.Clinical & Experimental Ophthalmology|April 21, 2021
"Blepharophimosis-plus" syndromes: Frequency of systemic genetic disorders that also include blepharophimosisDaphna Landau Prat, Brian J Nguyen, Alanna Strong, et al.Nature Genetics|November 25, 2025
Measurement and clinical interpretation of CRISPR off-targetsAriella Angelini Stewart, Rebecca C Ahrens-Nicklas, Shengdar Q Tsai, et al.Pageof 22