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Molecular Genetics and Metabolism|April 3, 2004
Cofactor treatment improves ATP synthetic capacity in patients with oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M Macdonald, et al.
Molecular Vision|May 3, 2014
Molecular genetic diagnostic techniques in choroideremiaMira J B Furgoch, Jacqueline Mewes-Arès, Alina Radziwon, et al.
Analytical Biochemistry|February 11, 2003
The use of lymphocytes to screen for oxidative phosphorylation disordersBarbara J Marriage, M Thomas Clandinin, Ian M MacDonald, et al.
Investigative Ophthalmology & Visual Science|September 8, 2018
Crystals and Fatty Acid Abnormalities Are Not Present in Circulating Cells From Choroideremia PatientsAlina Radziwon, Woo Jung Cho, Artur Szkotak, et al.
Ophthalmic Genetics|January 13, 2025
Inferior sectoral chorioretinopathy in two patients with novel heterozygous KIF11 mutationsAmit V Mishra, Rosanna Martens, Carolin Aizouki, et al.
Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|April 28, 2022
Ten-year analysis of traumatic open-globe injuries in Edmonton, Canada, from 2009-2018Stephen M Carrell, Scott Anderson, Matthew D Benson, et al.
Plastic Surgery (Oakville, Ont.)|September 2, 2025
Acquired Brown Syndrome as a Postoperative Complication of Orbital Wall Fracture Repair with Metallic MeshJustin J Lee, Nikhil Patil, Trent Schimmel, et al.
Progress in Retinal and Eye Research|July 10, 2022
Zebrafish and inherited photoreceptor disease: Models and insightsNicole C L Noel, W Ted Allison, Ian M MacDonald, et al.
Documenta Ophthalmologica. Advances in Ophthalmology|March 3, 2007
Choroideremia carriers maintain a normal electro-oculogram (EOG)Ryan J Yau, Christina A Sereda, Kerry E McTaggart, et al.
Retinal Cases & Brief Reports|November 13, 2014
De novo mutation in a choroideremia carrierSimge Bozbeyoglu, Gerald A Fishman, Edwin M Stone, et al.
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