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Neringa Jurkute

Showing results (1-10 of 35) with videos related to

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Handbook of Clinical Neurology|April 9, 2021
Electrophysiology in neuro-ophthalmologyNeringa Jurkute, Anthony G Robson
Current Opinion in Ophthalmology|June 27, 2017
Leber hereditary optic neuropathy: bridging the translational gapNeringa Jurkute, Patrick Yu-Wai-Man
Brain Sciences|November 24, 2022
The Role of the Inner Nuclear Layer for Perception of Persisting Tiling Inside a Monocular ScotomaRishikesh Gandhewar, Neringa Jurkute, Axel Petzold
Current Opinion in Neurology|December 6, 2018
Treatment strategies for Leber hereditary optic neuropathyNeringa Jurkute, Joshua Harvey, Patrick Yu-Wai-Man
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|July 16, 2018
Leber Hereditary Optic Neuropathy-Light at the End of the Tunnel?Ungsoo Samuel Kim, Neringa Jurkute, Patrick Yu-Wai-Man
Eye (London, England)|June 11, 2024
Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmologyAntonio Calcagni, Magella M Neveu, Neringa Jurkute, et al.
Cureus|March 13, 2026
Leber Hereditary Optic Neuropathy Caused by the Rare MT-ND1 m.3394T>C Mutation: A Case With Favorable Visual Prognosis and a Literature ReviewPaulina Mikulenaite, Alvita Vilkeviciute, Almina Stramkauskaite, et al.
Eye (London, England)|May 15, 2023
Mitochondria and the eye-manifestations of mitochondrial diseases and their managementBenson S Chen, Joshua P Harvey, Michael J Gilhooley, et al.
Orphanet Journal of Rare Diseases|October 10, 2025
Neuroretinal structure changes in infantile nephropathic cystinosisLeonie Franziska Keidel, Neringa Jurkute, Benedikt Schworm, et al.
Medicina (Kaunas, Lithuania)|March 3, 2021
A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.11253T>C</i>) and Literature ReviewRasa Liutkeviciene, Agne Sidaraite, Lina Kuliaviene, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Handbook of Clinical Neurology|April 9, 2021
Electrophysiology in neuro-ophthalmologyNeringa Jurkute, Anthony G Robson
Current Opinion in Ophthalmology|June 27, 2017
Leber hereditary optic neuropathy: bridging the translational gapNeringa Jurkute, Patrick Yu-Wai-Man
Brain Sciences|November 24, 2022
The Role of the Inner Nuclear Layer for Perception of Persisting Tiling Inside a Monocular ScotomaRishikesh Gandhewar, Neringa Jurkute, Axel Petzold
Current Opinion in Neurology|December 6, 2018
Treatment strategies for Leber hereditary optic neuropathyNeringa Jurkute, Joshua Harvey, Patrick Yu-Wai-Man
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|July 16, 2018
Leber Hereditary Optic Neuropathy-Light at the End of the Tunnel?Ungsoo Samuel Kim, Neringa Jurkute, Patrick Yu-Wai-Man
Eye (London, England)|June 11, 2024
Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmologyAntonio Calcagni, Magella M Neveu, Neringa Jurkute, et al.
Cureus|March 13, 2026
Leber Hereditary Optic Neuropathy Caused by the Rare MT-ND1 m.3394T>C Mutation: A Case With Favorable Visual Prognosis and a Literature ReviewPaulina Mikulenaite, Alvita Vilkeviciute, Almina Stramkauskaite, et al.
Eye (London, England)|May 15, 2023
Mitochondria and the eye-manifestations of mitochondrial diseases and their managementBenson S Chen, Joshua P Harvey, Michael J Gilhooley, et al.
Orphanet Journal of Rare Diseases|October 10, 2025
Neuroretinal structure changes in infantile nephropathic cystinosisLeonie Franziska Keidel, Neringa Jurkute, Benedikt Schworm, et al.
Medicina (Kaunas, Lithuania)|March 3, 2021
A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in <i>MT-ND4</i> Gene (<i>m.11253T>C</i>) and Literature ReviewRasa Liutkeviciene, Agne Sidaraite, Lina Kuliaviene, et al.
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