Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Genes|March 29, 2023
Evaluation of Genetic Testing in a Cohort of Diverse Pediatric Patients in the United States with Congenital CataractsJennifer L Rossen, Brenda L Bohnsack, Kevin X Zhang, et al.
BMC Ophthalmology|October 21, 2024
Evaluation of parameters for early detection of pediatric keratoconusSharon H Zhao, Carla Berkowitz, Hantamalala Ralay Ranaivo, et al.
Journal of Pediatric Ophthalmology and Strabismus|May 25, 2023
Leukemic Optic Neuropathy in Pediatric Patients: A Case SeriesGina M Johnson, Jennifer L Rossen, Shira S Simon, et al.
Ophthalmic Genetics|January 7, 2025
Genetic testing results of retinal dystrophies in a diverse population: impact of race and ethnicityCharles Miller, Brenda L Bohnsack, Andy Drackley, et al.
Archives of Physical Medicine and Rehabilitation|July 7, 2024
Risk Factors for Falls Among Hospitalized Medical Patients - A Systematic Review and Meta-analysisJeannelle Heinzmann, Michael L Rossen, Orestis Efthimiou, et al.
Genes|January 21, 2023
Diagnostic Yield of Genetic Testing for Ocular and Oculocutaneous Albinism in a Diverse United States Pediatric PopulationKyle S Chan, Brenda L Bohnsack, Alexander Ing, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|December 1, 2021
Long-term retinal vasculature abnormalities following intravitreal bevacizumab for retinopathy of prematurityAmir Sternfeld, Safa Rahmani, Jennifer L Rossen, et al.
Annals of Surgical Oncology|February 28, 2024
Assessment of Social Vulnerabilities of Care and Prognosis in Adult Ocular Melanomas in the USJoshua A Mensah, David J Fei-Zhang, Jennifer L Rossen, et al.
Ophthalmology. Retina|December 15, 2024
Ophthalmic Manifestations in a Diverse Pediatric Population with Type I and Type II Stickler SyndromeAndy Drackley, Hantamalala Ralay Ranaivo, Valerie Allegretti, et al.
American Journal of Medical Genetics. Part A|April 10, 2024
Ocular manifestations of CHARGE syndrome in a pediatric cohort with genotype/phenotype analysisKunal Kanwar, Saffiya Bashey, Brenda L Bohnsack, et al.
Pageof 5