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Title | Description | Subject | Collection |
1 |
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Atypical Leber Hereditary Optic Neuropathy: 18 Year Interval Between Eyes | | Biomedical Research; Databases, Factual; Eye Diseases; Humans; Neurology; Ophthalmology; Registries | Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu |
2 |
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Late-Onset Lebers Hereditary Optic Neuropathy | | Older people; DNA Mutational Analysis; Humans; Male; Optic Atrophies, Hereditary/diagnosis; Optic Atrophies, Hereditary/genetics; Point Mutation; Vision Disorders/diagnosis; Vision Disorders/genetics; Visual Acuity; Visual Fields | |
3 |
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Magnetic Resonance Findings in the Pregeniculate Visual Pathways in Leber Hereditary Optic Neuropathy | | Autonomic Fibers, Preganglionic; Genetic Predisposition to Disease; Humans; Magnetic Resonance Imaging; Male; Middle Older people; Optic Atrophy, Hereditary, Leber; Optic Nerve; Visual Pathways; Young Adult | |
4 |
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Leber Hereditary Optic Neuropathy- Some New Observations | | Autonomic Fibers, Preganglionic; Brachial Plexus Neuropathies; Brachial Plexus Neuropathies; Female; Humans; Magnetic Resonance Imaging; Male; Optic Atrophy, Hereditary, Leber; Optic Nerve; Peripheral Nervous System Diseases; Visual Pathways | |
5 |
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Vision Loss and Symmetric Basal Ganglia Lesions in Leber Hereditary Optic Neuropathy | | Adult; Basal Ganglia; Blindness; Disease Progression; Female; Humans; Magnetic Resonance Imaging; Optic Atrophy, Hereditary, Leber; Optic Chiasm; Optic Nerve; Visual Acuity | |
6 |
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Optic Nerve Enhancement on Orbital Magnetic Resonance Imaging in Lebers Hereditary Optic Neuropathy | | Adolescent; Humans; Male; Optic Atrophies, Hereditary/diagnosis; Optic Nerve/pathology; Orbit/pathology | |
7 |
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A Tale of Progressive Painless Vision Loss in a 64-Year-Old Man Due to Leber Hereditary Optic Neuropathy | | DNA, Mitochondrial / genetics; Humans; Male; Middle Aged; Optic Atrophy, Hereditary, Leber* / complications; Optic Atrophy, Hereditary, Leber* / diagnosis; Optic Atrophy, Hereditary, Leber* / genetics; Optic Nerve; Steroids; Tomography, Optical Coherence; Vision Disorders | |
8 |
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Leber Hereditary Optic Neuropathy Possibly Triggered by Exposure to Tire Fire | | Adult; Air Pollutants, adverse effects; Carbon, adverse effects; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial, genetics; Female; Genetic Predisposition to Disease, genetics; Humans; Male; Mutation, genetics; Optic Atrophy, Hereditary, Leber, diagnosis; Optic Atrophy, Heredita... | |
9 |
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Letters to the Editor | | | |
10 |
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Is Leber Hereditary Optic Neuropathy Treatable- Encouraging Results With Idebenone in Prospective and Retrospective Trials | | Optic Atrophy, Hereditary, Leber; Idebenone | |
11 |
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Is Leber Hereditary Optic Neuropathy Treatable- Encouraging Results With Idebenone in Prospective and Retrospective Trials | | Optic Atrophy, Hereditary, Leber; Idebenone | |
12 |
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Peripapillary Fluorescein Leakage in 11778 Lebers Optic Neuropathy | | Adolescent; Adult; Capillary Permeability; DNA, Mitochondrial/genetics; Female; Fluorescein; Fluorescein Angiography; Fluoresceins/metabolism; Fundus Oculi; Humans; Male; Optic Atrophies, Hereditary/diagnosis; Optic Atrophies, Hereditary/genetics; Optic Atrophies, Hereditary/physiopathology; Optic D... | |
13 |
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MRI of the Optic Nerves and Chiasm in Patients With Leber Hereditary Optic Neuropathy | | | |
14 |
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Mitochondrial DNA Hplogroup Distribution in Pedigrees of Southeast Asian G11778A Leber Hereditary Optic Neuropathy | | China, ethnology; DNA Mutational Analysis; DNA, Mitochondrial, genetics; Gene Frequency; Genetic Predisposition to Disease, genetics; Genetic Screening; Haplotypes; Humans; India, ethnology; Mutation, genetics; Optic Atrophy, Hereditary, Leber, ethnology; Optic Atrophy, Hereditary, Leber, genetics; ... | |
15 |
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International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy | | Antioxidants; Congresses as Topic; Consensus; Disease Management; Humans; International Cooperation; Ophthalmology; Optic Atrophy, Hereditary, Leber; Societies, Medical; Ubiquinone | |
16 |
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Reactive Oxygen Species in Mitochondrial Optic Neuropathies: Response | | Humans; Optic Chiasm; Optic Nerve Diseases; Scotoma; Superoxides | Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu |
17 |
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Cardiac Disorders in Patients With Leber Hereditary Optic Neuropathy | | | |
18 |
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Visual Outcomes in Leber Hereditary Optic Neuropathy Patients With the m.11778GA MTND4 Mitochondrial DNA Mutation | | | |
19 |
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A Family with Lebers Heredity Optic Neuropathy with Mitochondrial DNA Heteroplasmy Related to Disease Expression | | Adult; Older people; Older people, 80 and over; DNA/analysis; DNA Mutational Analysis; DNA Primers/chemistry; DNA, Mitochondrial/genetics; Female; Humans; Male; Middle Older people; Optic Atrophies, Hereditary/genetics; Optic Atrophies, Hereditary/physiopathology; Pedigree; Point Mutation; Polymeras... | |
20 |
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Do Idebenone and Vitamin Therapy Shorten the Time to Achieve Visual Recovery in Leber Hereditary Optic Neuropathy | | Adolescent; Adult; Age of Onset; Antioxidants/therapeutic use; Ascorbic Acid/therapeutic use; Benzoquinones/therapeutic use; Drug Therapy, Combination; Female; Follow-Up Studies; Humans; Male; Middle Older people; Mutation; Optic Atrophies, Hereditary/complications; Optic Atrophies, Hereditary/drug ... | |
21 |
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Energy Charge Is Not Decreased in Lymphocytes of Patients with Lebers Hereditary Optic Neuropathy with the 11778 Mutation | | Adenosine Diphosphate/metabolism; Adenosine Monophosphate/metabolism; Adenosine Triphosphate/metabolism; Chromatography, High Pressure Liquid; DNA, Mitochondrial/genetics; DNA, Mitochondrial/metabolism; Humans; Lymphocytes/metabolism; Optic Atrophies, Hereditary/genetics; Optic Atrophies, Hereditary... | |
22 |
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Are We There Yet? Is Neuro-Ophthalmology at the Cuspof a Paradigm Shift? Lessons From Leber Hereditary Optic Neuropathy | | Humans; Mitochondria; Neurology; Ophthalmology; Optic Atrophy, Hereditary, Leber; Optic Nerve; Reactive Oxygen Species | |
23 |
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Leber Hereditary Optic Neuropathy in a Mother and Daughter Associated With m.10197G>A Mutation | | | |
24 |
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Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations | | | |
25 |
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Clinical Features of Chinese Sporadic Leber Hereditary Optic Neuropathy Caused by Rare Primary mtDNA Mutations | | | |