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Showing results (261-270 of 293) with videos related to

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Investigative Ophthalmology & Visual Science|July 2, 2026
Archetypal Visual Field Analysis of Patients With Chronic Leber Hereditary Optic Neuropathy in Relation to Visual RecoveryCatarina P Coutinho, Ferdinando Zanchetta, Michele Carbonelli, et al.
Plos One|July 15, 2020
Correction: Retinal nerve fiber layer thickness predicts CSF amyloid/tau before cognitive declineSamuel Asanad, Michele Fantini, William Sultan, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|August 20, 2021
Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE StudyValérie Biousse, Nancy J Newman, Patrick Yu-Wai-Man, et al.
JAMA Ophthalmology|December 19, 2024
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic NeuropathyPatrick Yu-Wai-Man, Nancy J Newman, Valérie Biousse, et al.
Plos One|May 30, 2020
Retinal nerve fiber layer thickness predicts CSF amyloid/tau before cognitive declineSamuel Asanad, Michele Fantini, William Sultan, et al.
Mitochondrion|June 11, 2013
Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal lossFred N Ross-Cisneros, Billy X Pan, Ruwan A Silva, et al.
American Journal of Human Genetics|March 15, 2006
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigreesValerio Carelli, Alessandro Achilli, Maria Lucia Valentino, et al.
Mitochondrion|August 14, 2021
The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypesVeria Vacchiano, Leonardo Caporali, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 10, 2017
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic NeuropathyValerio Carelli, Michele Carbonelli, Irenaeus F de Coo, et al.
Pageof 30

Showing results (261-270 of 293) with videos related to

Sort By:
Pageof 30
Investigative Ophthalmology & Visual Science|July 2, 2026
Archetypal Visual Field Analysis of Patients With Chronic Leber Hereditary Optic Neuropathy in Relation to Visual RecoveryCatarina P Coutinho, Ferdinando Zanchetta, Michele Carbonelli, et al.
Plos One|July 15, 2020
Correction: Retinal nerve fiber layer thickness predicts CSF amyloid/tau before cognitive declineSamuel Asanad, Michele Fantini, William Sultan, et al.
Investigative Ophthalmology & Visual Science|June 6, 2013
The pupil light reflex in Leber's hereditary optic neuropathy: evidence for preservation of melanopsin-expressing retinal ganglion cellsAna Laura A Moura, Balázs V Nagy, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|August 20, 2021
Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE StudyValérie Biousse, Nancy J Newman, Patrick Yu-Wai-Man, et al.
JAMA Ophthalmology|December 19, 2024
Five-Year Outcomes of Lenadogene Nolparvovec Gene Therapy in Leber Hereditary Optic NeuropathyPatrick Yu-Wai-Man, Nancy J Newman, Valérie Biousse, et al.
Plos One|May 30, 2020
Retinal nerve fiber layer thickness predicts CSF amyloid/tau before cognitive declineSamuel Asanad, Michele Fantini, William Sultan, et al.
Mitochondrion|June 11, 2013
Optic nerve histopathology in a case of Wolfram Syndrome: a mitochondrial pattern of axonal lossFred N Ross-Cisneros, Billy X Pan, Ruwan A Silva, et al.
American Journal of Human Genetics|March 15, 2006
Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigreesValerio Carelli, Alessandro Achilli, Maria Lucia Valentino, et al.
Mitochondrion|August 14, 2021
The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypesVeria Vacchiano, Leonardo Caporali, Chiara La Morgia, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|October 10, 2017
International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic NeuropathyValerio Carelli, Michele Carbonelli, Irenaeus F de Coo, et al.
Pageof 30