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  1. 41
    “…BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited blinding disorder, which in over 90% of cases is due to one of three primary mitochondrial DNA (mtDNA) point mutations (m.11778G>A, m.3460G>A and m.14484T>C, respectively in MT-ND4, MT-ND1 and MT-ND6 genes). …”
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    Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy
  2. 42
    “…BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disease that typically causes bilateral blindness in young men. …”
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    Leber’s hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patients
  3. 43
    “…Leber’s hereditary optic neuropathy (LHON) is a mitochondrially inherited disease leading to blindness. …”
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    Efficacy and Safety of rAAV2-ND4 Treatment for Leber’s Hereditary Optic Neuropathy
  4. 44
    “…The objective of this study is to investigate the characteristics and the evolution of visual field damage caused by Leber’s hereditary optic neuropathy (LHON) and to provide clinical data for the diagnosis of LHON. …”
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    A retrospective analysis of characteristics of visual field damage in patients with Leber’s hereditary optic neuropathy
  5. 45
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    Psychological morbidity in Leber’s hereditary optic neuropathy depends on phenotypic, social, economic, and genetic factors
  6. 46
    “…Leber’s hereditary optic neuropathy (LHON) is one of the most common mitochondrial diseases caused by point mutations in mitochondrial DNA (mtDNA). …”
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    Testosterone increases apoptotic cell death and decreases mitophagy in Leber’s hereditary optic neuropathy cells
  7. 47
    “…BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited mitochondrial disease, characterized by acute or subacute, painless, bilateral visual loss. …”
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    Leber’s hereditary optic neuropathy following unilateral painful optic neuritis: a case report
  8. 48
    “…Leber’s hereditary optic neuropathy (LHON) is one of the mitochondrial diseases that causes loss of central vision, progressive impairment and subsequent degeneration of retinal ganglion cells (RGCs). …”
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    Neuroanatomical Changes in Leber’s Hereditary Optic Neuropathy: Clinical Application of 7T MRI Submillimeter Morphometry
  9. 49
    “…BACKGROUND: Leber’s hereditary optic neuropathy (LHON) is a common form of mitochondrial disease. …”
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    Magnetic resonance imaging negative myelopathy in Leber’s hereditary optic neuropathy: a case report
  10. 50
    Libro
    Labor economics and labor relations /
  11. 51
    “…Leber’s hereditary optic neuropathy (LHON) is a disease that affects the optical nerve, causing visual loss. …”
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    Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber’s Hereditary Optic Neuropathy (LHON) Subjects
  12. 52
    “…Background: Leber’s hereditary optic neuropathy (LHON) is a rare disease. …”
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    Leber’s Hereditary Optic Neuropathy (LHON): Clinical Experience and Outcomes after Long-Term Idebenone Treatment
  13. 53
    “…BACKGROUND: During the first few trials of gene therapy for Leber’s hereditary optic neuropathy performed by our group, the visual acuity of the patients increased gradually over several months, or even years. …”
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    Three Cases of Leber’s Hereditary Optic Neuropathy with Rapid Increase in Visual Acuity After Gene Therapy
  14. 54
    por Jonak, Kamil
    Publicado 2020
    “…Leber’s hereditary optic neuropathy (LHON) is a rare, maternally inherited genetic disease caused by a mutation of mitochondrial DNA. …”
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    Widespread Reductions of Spontaneous Neurophysiological Activity in Leber’s Disease—An Application of EEG Source Current Density Reconstruction
  15. 55
    “…BACKGROUND: Limited studies have identified the changes in peripapillary retinal nerve fibre layer (pRNFL) thickness in patients with chronic Leber’s hereditary optic neuropathy (LHON) at different stages of the disease. …”
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    Characterisation of thickness changes in the peripapillary retinal nerve fibre layer in patients with Leber’s hereditary optic neuropathy
  16. 56
    “…BACKGROUIND: Leber’s hereditary optic neuropathy (LHON) is a mitochondrial disease characterized by bilateral severe subacute central vision loss and a mutation in the mitochondrial DNA (mtDNA). …”
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    Leber’s hereditary optic neuropathy with diffuse white matter changes mimicking gliomatosis cerebri: illustrative case
  17. 57
    “…BACKGROUND: In Leber’s hereditary optic neuropathy (LHON), mtDNA mutations mediate mitochondrial dysfunction and apoptosis of retinal ganglion cells. …”
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    Superoxide dismutase 2 ameliorates mitochondrial dysfunction in skin fibroblasts of Leber’s hereditary optic neuropathy patients
  18. 58
    “…Background and Objectives: To evaluate the association of relative leukocyte telomere length (RLTL) and telomerase complex regulatory markers with Leber’s hereditary optic neuropathy (LHON). Material and Methods: A case-control study was performed in patients with LHON (≥18 years) and healthy subjects. …”
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    Relative Leukocyte Telomere Length and Telomerase Complex Regulatory Markers Association with Leber’s Hereditary Optic Neuropathy
  19. 59
    “…Leber’s Hereditary Optic Neuropathy (LHON) is the most common primary mitochondrial DNA disorder. …”
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    Solutions to a Radical Problem: Overview of Current and Future Treatment Strategies in Leber’s Hereditary Opic Neuropathy
  20. 60
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    Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
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