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Ophthalmic Genetics|August 4, 2011
Phenotype and genotype of patients with autosomal recessive bestrophinopathyIan M MacDonald, H V Gudiseva, Adda Villanueva, et al.
American Journal of Ophthalmology Case Reports|August 22, 2018
A diagnosis of Stevens-Johnson Syndrome (SJS) in a patient presenting with superficial keratitisForson Chan, Matthew D Benson, David J A Plemel, et al.
Ophthalmic Plastic and Reconstructive Surgery|December 14, 2020
Nonosseous Periocular Manifestations of Langerhans Cell Histiocytosis: A Case Report and Systematic ReviewDavid J A Plemel, Matthew D Benson, C Maya Tong, et al.
Investigative Ophthalmology & Visual Science|March 20, 2012
Dietary docosahexaenoic acid supplementation prevents age-related functional losses and A2E accumulation in the retinaBlake Dornstauder, Miyoung Suh, Sharee Kuny, et al.
Cells|October 3, 2020
Progressive Photoreceptor Dysfunction and Age-Related Macular Degeneration-Like Features in rp1l1 Mutant ZebrafishNicole C L Noel, Nathan J Nadolski, Jennifer C Hocking, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|March 1, 2003
Autosomal dominant macular dystrophy in a large Canadian familyLarry A Donoso, Gregory Hageman, Arcilee Frost, et al.
American Journal of Medical Genetics. Part A|February 19, 2026
Identification of Two Novel Mutations in the CHM Gene Causing ChoroideremiaFarshad Niri, Alina Radziwon, Rachel Mah, et al.
Translational Vision Science & Technology|July 28, 2020
Perspectives on Gene Therapy: Choroideremia Represents a Challenging Model for the Treatment of Other Inherited Retinal DegenerationsIan M MacDonald, Christopher Moen, Jacque L Duncan, et al.
Human Mutation|August 31, 2002
Mutational analysis of patients with the diagnosis of choroideremiaKerry E McTaggart, Mai Tran, Dean Y Mah, et al.
Ophthalmic Genetics|November 8, 2005
A new case of oculoectodermal syndromeThomas K M Lee, Royce L C Johnson, Ian M MacDonald, et al.
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