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Ophthalmic Genetics|October 21, 2003
Electrophysiology and ocular blood flow in a family with dominant optic nerve atrophy and a mutation in the OPA1 geneLotta Gränse, Ingar Bergstrand, Dawn Thiselton, et al.Journal of Medicinal Chemistry|November 12, 2020
Discovery of Novel 2-Aniline-1,4-naphthoquinones as Potential New Drug Treatment for Leber's Hereditary Optic Neuropathy (LHON)Carmine Varricchio, Kathy Beirne, Pascale Aeschlimann, et al.Investigative Ophthalmology & Visual Science|May 3, 2019
The Relationship Between the Photopic Negative Response and Retinal Ganglion Cell TopographyEnyam Komla A Morny, Kishan Patel, Marcela Votruba, et al.Brain : a Journal of Neurology|February 4, 2012
Opa1 is essential for retinal ganglion cell synaptic architecture and connectivityPete A Williams, Malgorzata Piechota, Christopher von Ruhland, et al.Acta Neuropathologica|October 4, 2016
A neurodegenerative perspective on mitochondrial optic neuropathiesPatrick Yu-Wai-Man, Marcela Votruba, Florence Burté, et al.Acta Ophthalmologica|November 19, 2016
OPA1 analysis in an international series of probands with bilateral optic atrophyPetra Liskova, Marketa Tesarova, Lubica Dudakova, et al.Acta Ophthalmologica|February 8, 2013
Novel OPA1 missense mutation in a family with optic atrophy and severe widespread neurological disorderPetra Liskova, Olga Ulmanova, Petr Tesina, et al.Investigative Ophthalmology & Visual Science|May 16, 2009
Secondary mtDNA defects do not cause optic nerve dysfunction in a mouse model of dominant optic atrophyPatrick Yu-Wai-Man, Vanessa J Davies, Malgorzata J Piechota, et al.Acta Ophthalmologica|September 28, 2018
Peripapillary microcirculation in Leber hereditary optic neuropathyBohdan Kousal, Hana Kolarova, Martin Meliska, et al.Plos One|February 15, 2013
Non-image-forming light driven functions are preserved in a mouse model of autosomal dominant optic atrophyGeorgia Perganta, Alun R Barnard, Christiana Katti, et al.Pageof 6