Two-Year Results After AAV2-Mediated Gene Therapy for Choroideremia: The Alberta Experience von Dimopoulos, Ioannis S., Hoang, Stephanie C., Radziwon, Alina, Binczyk, Natalia M., Seabra, Miguel C., MacLaren, Robert E., Somani, Rizwan, Tennant, Matthew T.S., MacDonald, Ian M.

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Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling von Havrylov, Serhiy, Chrystal, Paul, van Baarle, Suey, French, Curtis R., MacDonald, Ian M., Avasarala, Jagannadha, Rogers, R. Curtis, Berry, Fred B., Kume, Tsutomu, Waskiewicz, Andrew J., Lehmann, Ordan J.

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Zebrafish Models of Photoreceptor Dysfunction and Degeneration von Noel, Nicole C L, MacDonald, Ian M, Allison, W Ted

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Ocular Gene Therapy with Adeno-associated Virus Vectors: Current Outlook for Patients and Researchers von Casey, Geoffrey A, Papp, Kimberly M, MacDonald, Ian M

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Choroideremia: New Findings from Ocular Pathology and Review of Recent Literature von MacDonald, Ian M., MD, CM, Russell, Laurie, MD, Chan, Chi-Chao, MD

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Visual Field Progression in Retinitis Pigmentosa von Xu, Manlong, Zhai, Yi, MacDonald, Ian M

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Loss-of-function mutations in Rab escort protein 1 (REP-1) affect intracellular transport in fibroblasts and monocytes of choroideremia patients von Strunnikova, Natalia V, Barb, Jennifer, Sergeev, Yuri V, Thiagarajasubramanian, Ashwin, Silvin, Christopher, Munson, Peter J, Macdonald, Ian M

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Progressive Photoreceptor Dysfunction and Age-Related Macular Degeneration-Like Features in rp1l1 Mutant Zebrafish von Noel, Nicole C. L., Nadolski, Nathan J., Hocking, Jennifer C., MacDonald, Ian M., Allison, W. Ted

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Genetic variants in PIKFYVE: A review of ocular phenotypes von Misaghi, Ehsan, Kannu, Peter, MacDonald, Ian M., Benson, Matthew D.

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Improved electroretinographic responses following dietary intervention in a patient with Refsum disease von Benson, Matthew D., MacDonald, Ian M., Sheehan, Melissa, Jain, Shailly

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High-throughput retina-array for screening 93 genes involved in inherited retinal dystrophy von Song, Jin, Smaoui, Nizar, Ayyagari, Radha, Stiles, David, Benhamed, Sonia, MacDonald, Ian M, Daiger, Stephen P, Tumminia, Santa J, Hejtmancik, Fielding, Wang, Xinjing

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Upward saccadic intrusions as the presenting feature for incomplete congenital stationary night blindness von Aghazadeh, Helya, MacDonald, Ian M., Jivraj, Imran

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OCT Changes in 4-Year-Old Choroideremia Patient von Zhai, Yi, MacDonald, Ian M.

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A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness von Riazuddin, S. Amer, Shahzadi, Amber, Zeitz, Christina, Ahmed, Zubair M., Ayyagari, Radha, Chavali, Venkata R.M., Ponferrada, Virgilio G., Audo, Isabelle, Michiels, Christelle, Lancelot, Marie-Elise, Nasir, Idrees A., Zafar, Ahmad U., Khan, Shaheen N., Husnain, Tayyab, Jiao, Xiaodong, MacDonald, Ian M., Riazuddin, Sheikh, Sieving, Paul A., Katsanis, Nicholas, Hejtmancik, J. Fielding

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RP1L1 and inherited photoreceptor disease: A review von Noel, Nicole C.L., MacDonald, Ian M.

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Microperimetry as an Outcome Measure in Choroideremia Trials: Reproducibility and Beyond von Dimopoulos, Ioannis S, Tseng, Calvin, MacDonald, Ian M

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Iris Flocculi Investigated for Familial Thoracic Aortic Aneurysms and Dissections von MacDonald, Ian M., Modeste, Deborah, MacPherson, Melissa J.

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Breaking bad news in ophthalmology: a pilot skills workshop for residents von Papp, Kimberly M., MacDonald, Ian M.

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Breaking Bad News in Eye Care von PAPP, KIMBERLY M., GRACIE, SARA K., MACDONALD, IAN M.

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The Need for Standardization of Antiretinal Antibody Detection and Measurement von Forooghian, Farzin, MacDonald, Ian M, Heckenlively, John R, Héon, Elise, Gordon, Lynn K, Hooks, John J, Detrick, Barbara, Nussenblatt, Robert B

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