Disease: Leber Hereditary Optic Neuropathy
- <em>DNAJC30</em> Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients
- A challenging differential diagnosis - Leber's Hereditary Optic Neuropathy
- A Japanese Case of Leber's Hereditary Optic Neuropathy with the m.13051G>A Pathogenic Variant
- A Japanese Case of Leber's Hereditary Optic Neuropathy with the m.13051G>A Pathogenic Variant
- A rare, likely pathogenic variant causing Leber's hereditary optic neuropathy in three-generation females of an African-American family
- Alstrom's Syndrome, Leber's Hereditary Optic Neuropathy, or Retinitis Pigmentosa? A Case of Misdiagnosis
- An atypical presentation of Leber's hereditary optic neuropathy in childhood
- Approaches to the epidemiology of NOHL in the region of Madrid: Survey of neuro-ophthalmologists
- Autosomal Recessive Leber Hereditary Optic Neuropathy in a Patient With a Novel NDUFAF2 Compound Heterozygous Mutation
- Autosomal Recessive Leber Hereditary Optic Neuropathy Triggered by Superior Mesenteric Artery Syndrome
- Autosomal recessive Leber's hereditary optic neuropathy caused by a homozygous variant in DNAJC30 gene
- Bench to Bedside: Rapid Leber Hereditary Optic Neuropathy Diagnosis
- Case report: Mutations in <em>DNAJC30</em> causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals
- Case report: Mutations in DNAJC30 causing autosomal recessive Leber hereditary optic neuropathy are common amongst Eastern European individuals
- Choriocapillaris and choroidal thickness in all Leber hereditary optic neuropathy stages using swept source technology
- Clinical Characteristics of m.11778G>A Leber Hereditary Optic Neuropathy with Favorable Outcomes
- Clinical Profile of Patients with Leber Hereditary Optic Neuropathy-An Ambispective Study in Cohort from Northern Part of India
- Clinically Diagnosed Occult Macular Dystrophy Habouring an m.14502T>C Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy: Case Report and Literature Review
- Clinically Diagnosed Occult Macular Dystrophy Habouring an m.14502T>C Mitochondrial DNA Mutation Associated with Leber's Hereditary Optic Neuropathy: Case Report and Literature Review
- Coenzyme Q10 trapping in mitochondrial complex I underlies Leber's hereditary optic neuropathy
- Correction to: Mitophagy activation repairs Leber's hereditary optic neuropathy-associated mitochondrial dysfunction and improves cell survival
- Correlation between Residual Sensitivity in the Central Inferior Nasal Visual Field and Visual Function in Chronic Leber Hereditary Optic Neuropathy Patients
- COVID-19 Disease: A Trigger for Leber Hereditary Optic Neuropathy (LHON)
- Current and Future Landscape in Genetic Therapies for Leber Hereditary Optic Neuropathy
- Development of a deep learning model to distinguish the cause of optic disc atrophy using retinal fundus photography
- Diagnostic Yield of Investigations in Symmetric Optic Neuropathy
- Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant
- DNAJC30 Gene Variants Are a Frequent Cause of a Rare Disease: Leber Hereditary Optic Neuropathy in Polish Patients
- Dysregulation of the circRNA_0087207/miR-548c-3p/PLSR1-TGFB2 axis in Leber hereditary optic neuropathy in vitro
- Dysregulation of the circRNA_0087207/miR-548c-3p/PLSR1-TGFB2 axis in Leber's hereditary optic neuropathy in vitro
- Elamipretide Topical Ophthalmic Solution for the Treatment of Subjects with Leber Hereditary Optic Neuropathy: A Randomized Trial
- Elamipretide Topical Ophthalmic Solution for the Treatment of Subjects With Leber's Hereditary Optic Neuropathy: A Randomized Trial
- Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
- Epigenetic regulation of the nuclear genome associated with mitochondrial dysfunction in Leber's hereditary optic neuropathy (LHON)
- Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber's Hereditary Optic Neuropathy (LHON) Subjects
- Exploring mito-nuclear genetic factors in Leber's hereditary optic neuropathy: insights from comprehensive profiling of unique cases
- Gene augmentation in FAM161A ciliopathy: Toward functional vision rescue
- Gene therapy for mitochondrial disorders
- Generation of iPSCs from identical twin, one affected by LHON and one unaffected, both carrying a combination of two mitochondrial variants: m.14484 T>C and m.10680G>A
- Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy
- Hereditary Optic Neuropathies: A Systematic Review on the Interplay between Biomaterials and Induced Pluripotent Stem Cells
- Hereditary optic neuropathy associated with demyelinating diseases of the central nervous system
- HLA-Homozygous iPSC-Derived Mesenchymal Stem Cells Rescue Rotenone-Induced Experimental Leber's Hereditary Optic Neuropathy-like Models In Vitro and In Vivo
- How defective mitochondrial electrical activity leads to inherited blindness
- Identification and characterization of a new pathologic mutation in a large Leber hereditary optic neuropathy pedigree
- Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
- Injectable, Antioxidative, and Tissue-Adhesive Nanocomposite Hydrogel as a Potential Treatment for Inner Retina Injuries
- Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia
- Leber hereditary optic neuropathy gene therapy
- Leber Hereditary Optic Neuropathy Gene Therapy: Longitudinal Relationships Among Visual Function and Anatomical Measures
- Leber Hereditary Optic Neuropathy Gene Therapy: Longitudinal Relationships Among Visual Function and Anatomical Measures: LHON Gene Therapy: Visual Function and Anatomical Measures
- Leber Hereditary Optic Neuropathy in 2 Sisters With Friedreich Ataxia
- Leber Hereditary Optic Neuropathy Plus Phenotype With Double Point Mutations (m.11778 G>A and m.14484T>C) and Concurrent Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease (MOGAD)
- Leber hereditary optic neuropathy presenting as bilateral visual loss and white matter disease
- Leber Hereditary Optic Neuropathy Triggered by Idiopathic Intracranial Hypertension
- Leber's hereditary optic neuropathy
- Leber's Hereditary Optic Neuropathy (LHON): Clinical Experience and Outcomes after Long-Term Idebenone Treatment
- Leber's hereditary optic neuropathy and epilepsy in a female monozygotic twin
- Leber's hereditary optic neuropathy associated with idiopathic intracranial hypertension
- Leber's Hereditary Optic Neuropathy in a Nonagenarian
- Leber's hereditary optic neuropathy: Update on the novel genes and therapeutic options
- Letter to the editor on: prophylactic nicotinamide treatment protects from rotenone-induced neurodegeneration by increasing mitochondrial content and volume
- Letter to the Editor: Retinal morphological and functional response to Idebenone therapy in Leber hereditary optic neuropathy
- Long-term changes in morphological and functional parameters of the optic nerve in patients with various genetic variants of hereditary optic neuropathies
- Mitochondrial DNA 13513G>A Mutation Causing Leber Hereditary Optic Neuropathy Associated With Adult-Onset Renal Failure
- Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy
- Mitochondrially Targeted Gene Therapy Rescues Visual Loss in a Mouse Model of Leber's Hereditary Optic Neuropathy
- Mutation at the entrance of the quinone cavity severely disrupts quinone binding in respiratory complex I
- Neuroimaging changes in the pregeniculate visual pathway and chiasmal enlargement in Leber hereditary optic neuropathy
- Neuroprotective Effect of Tauroursodeoxycholic Acid (TUDCA) on In Vitro and In Vivo Models of Retinal Disorders: A Systematic Review
- Optimized allotopic expression of mitochondrial ND6 transgene restored complex I and apoptosis deficiencies caused by LHON-linked ND6 14484T > C mutation
- Oxidative Stress: A Suitable Therapeutic Target for Optic Nerve Diseases?
- Pathogenicity of Variant m.13528A>G in <em>MT-ND5</em> in Leber's Hereditary Optic Neuropathy Is Unsupported
- Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber's Hereditary Optic Neuropathy Is Unsupported
- Pearls & Oy-sters: Leber Hereditary Optic Neuropathy-Plus Masquerading as Neuromyelitis Optica Spectrum Disorder in a 2-Year-Old Child
- Pearls & Oy-sters: Leber Hereditary Optic Neuropathy-Plus Masquerading as Neuromyelitis Optica Spectrum Disorder in a 2-Year-Old Child
- Peripapillary hyperreflective ovoid mass-like structures (PHOMS) in patients with acute Leber's hereditary optic neuropathy
- Peripapillary hyperreflective ovoid mass-like structures: multimodal imaging and associated diseases
- Peripapillary retinal nerve fibre layer thinning, perfusion changes and optic neuropathy in carriers of Leber hereditary optic neuropathy-associated mitochondrial variants
- Photobiomodulation Using Light-Emitting Diode (LED) for Treatment of Retinal Diseases
- Poor visual prognosis of Asian patients with 3460 mitochondrial DNA mutation in Leber's hereditary optic neuropathy
- Progress in diagnosis and treatment of Leber's hereditary optic neuropathy
- Prophylactic nicotinamide treatment protects from rotenone-induced neurodegeneration by increasing mitochondrial content and volume
- Pushing Retinal Imaging Forward: Innovations and Their Clinical Meaning - The 2022 Ophthalmologica Lecture
- Pushing Retinal Imaging Forward: Innovations and their Clinical Meaning. The 2022 Ophthalmologica Lecture
- Pyrroloquinoline quinone drives ATP synthesis in vitro and in vivo and provides retinal ganglion cell neuroprotection
- Rapid and Sensitive Diagnosis of Leber Hereditary Optic Neuropathy Variants Using CRISPR/Cas12a Detection
- Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary optic neuropathy
- RatioCRISPR: A ratiometric biochip based on CRISPR/Cas12a for automated and multiplexed detection of heteroplasmic SNPs in mitochondrial DNA
- Recessive <em>MECR</em> pathogenic variants cause an LHON-like optic neuropathy
- Recessive MECR pathogenic variants cause an LHON-like optic neuropathy
- Recurrence of Visual Loss in Recessive Leber Hereditary Optic Neuropathy: New Paradigm
- Response to "Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber's Hereditary Optic Neuropathy Is Unsupported"
- Response to "Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber's Hereditary Optic Neuropathy Is Unsupported"
- Safety and Efficacy of Adeno-Associated Viral Gene Therapy in Patients With Retinal Degeneration: A Systematic Review and Meta-Analysis
- The genetic puzzle of a SOD1-patient with ocular ptosis and a motor neuron disease: a case report
- The Optic Nerve at Stake: Update on Environmental Factors Modulating Expression of Leber's Hereditary Optic Neuropathy
- The Potential and Application of iPSCs in Gene and Cell Therapy for Retinopathies and Optic Neuropathies
- Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial
- Variant and clinical landscape of Leber hereditary optic neuropathy based on 1516 families with mtDNA variants in a tertiary centre