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Patrick Yu

Showing results (171-180 of 183) with videos related to

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Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Neurology|December 16, 2016
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutationsChunyan Liao, Neil Ashley, Alan Diot, et al.
Nature Medicine|September 15, 2022
A digital mask to safeguard patient privacyYahan Yang, Junfeng Lyu, Ruixin Wang, et al.
Brain : a Journal of Neurology|December 27, 2013
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathyCarla Giordano, Luisa Iommarini, Luca Giordano, et al.
Investigative Ophthalmology & Visual Science|February 23, 2021
Associations Between Regional Environment and Cornea-Related Morphology of the Eye in Young Adults: A Large-Scale Multicenter Cross-Sectional StudyJiaonan Ma, Lanqin Zhao, Yahan Yang, et al.
Brain : a Journal of Neurology|April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenanceGerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
The New England Journal of Medicine|April 15, 2020
Artificial Intelligence to Detect Papilledema from Ocular Fundus PhotographsDan Milea, Raymond P Najjar, Jiang Zhubo, et al.
Brain Communications|September 1, 2021
Pathogenic <i>NR2F1</i> variants cause a developmental ocular phenotype recapitulated in a mutant mouse modelNeringa Jurkute, Michele Bertacchi, Gavin Arno, et al.
Brain : a Journal of Neurology|November 14, 2025
Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophyClaudio Fiorini, Neringa Jurkute, Alessandra Torraco, et al.
Nature Medicine|January 26, 2023
Early detection of visual impairment in young children using a smartphone-based deep learning systemWenben Chen, Ruiyang Li, Qinji Yu, et al.
Pageof 19

Showing results (171-180 of 183) with videos related to

Sort By:
Pageof 19
Brain Communications|May 31, 2021
Dominant <i>ACO2</i> mutations are a frequent cause of isolated optic atrophyMajida Charif, Naïg Gueguen, Marc Ferré, et al.
Neurology|December 16, 2016
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutationsChunyan Liao, Neil Ashley, Alan Diot, et al.
Nature Medicine|September 15, 2022
A digital mask to safeguard patient privacyYahan Yang, Junfeng Lyu, Ruixin Wang, et al.
Brain : a Journal of Neurology|December 27, 2013
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathyCarla Giordano, Luisa Iommarini, Luca Giordano, et al.
Investigative Ophthalmology & Visual Science|February 23, 2021
Associations Between Regional Environment and Cornea-Related Morphology of the Eye in Young Adults: A Large-Scale Multicenter Cross-Sectional StudyJiaonan Ma, Lanqin Zhao, Yahan Yang, et al.
Brain : a Journal of Neurology|April 15, 2014
Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenanceGerald Pfeffer, Gráinne S Gorman, Helen Griffin, et al.
The New England Journal of Medicine|April 15, 2020
Artificial Intelligence to Detect Papilledema from Ocular Fundus PhotographsDan Milea, Raymond P Najjar, Jiang Zhubo, et al.
Brain Communications|September 1, 2021
Pathogenic <i>NR2F1</i> variants cause a developmental ocular phenotype recapitulated in a mutant mouse modelNeringa Jurkute, Michele Bertacchi, Gavin Arno, et al.
Brain : a Journal of Neurology|November 14, 2025
Recessive variants in mitochondrial Complex I nuclear subunits are an underrated cause of optic atrophyClaudio Fiorini, Neringa Jurkute, Alessandra Torraco, et al.
Nature Medicine|January 26, 2023
Early detection of visual impairment in young children using a smartphone-based deep learning systemWenben Chen, Ruiyang Li, Qinji Yu, et al.
Pageof 19