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 case for the use of chemotherapy in hereditary mitochondrial optic neuropathies: Successful administration of cisplatin/etoposide in a male patient with testicular seminoma and Leber's hereditary optic neuropathy
- A challenging differential diagnosis - Leber's Hereditary Optic Neuropathy
- A Comprehensive Review of Leber Hereditary Optic Neuropathy and Its Association with Multiple Sclerosis-Like Phenotypes Known as Harding's Disease
- A computational study to assess the pathogenicity of single or combinations of missense variants on respiratory complex I
- 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
- Assessment of objective visual function following idebenone administration in patients with leber hereditary optic neuropathy
- Atypical Late-Onset Leber Hereditary Optic Neuropathy (LHON) Associated With T14484C Mutation
- Autosomal recessive leber hereditary optic neuropathy in a choroideremia carrier. A case report
- 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
- 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 follow-up investigation on thickness changes in the peripapillary retinal nerve fibre layer of patients with Leber hereditary optic neuropathy
- 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
- Co-occurrence of glial fibrillary acidic protein astrocytopathy in a patient with Leber's hereditary optic neuropathy due to DNAJC30 mutations
- 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)
- Deep Brain Stimulation for Medication Refractory Tremor in Leber Optic Neuropathy Plus Syndrome
- Development of a deep learning model to distinguish the cause of optic disc atrophy using retinal fundus photography
- 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 mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutation
- 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
- Electrodiagnostic tests of the visual pathway and applications in neuro-ophthalmology
- 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)
- Exploring mito-nuclear genetic factors in Leber's hereditary optic neuropathy: insights from comprehensive profiling of unique cases
- Extensive Optic Tracts Involvement in the Acute Phase of Leber Hereditary Optic Neuropathy
- Extranuclear DNA Variations in the Susceptibility of Glaucoma
- Family Planning in Genetic Optic Atrophies in Israel, a Case Series and a Discussion of Ethical Considerations
- Galactose-replacement unmasks the biochemical consequences of the G11778A mitochondrial DNA mutation of LHON in patient-derived fibroblasts
- Gene therapy for Leber hereditary optic neuropathy
- 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
- 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
- Impaired mitochondrial morphological plasticity and failure of mitophagy associated with the G11778A mutation of LHON
- Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
- Inhibition of angiogenesis by the secretome from iPSC-derived retinal ganglion cells with Leber's hereditary optic neuropathy-like phenotypes
- Injectable, Antioxidative, and Tissue-Adhesive Nanocomposite Hydrogel as a Potential Treatment for Inner Retina Injuries
- Leber Hereditary Optic Neuropathy (LHON)
- Leber Hereditary Optic Neuropathy (LHON) in Patients with Presumed Childhood Monocular Amblyopia
- Leber Hereditary Optic Neuropathy Case Report: Clinical Presentation and Treatment with Idebenone Reinforce the Evidence for m.3866T>C as a Causative Variant
- Leber hereditary optic neuropathy gene therapy
- Leber Hereditary Optic Neuropathy in 2 Sisters With Friedreich Ataxia
- Leber hereditary optic neuropathy in Czechia and Slovakia: Quality of life and costs from patient perspective
- 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 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 in a Nonagenarian
- Leber's hereditary optic neuropathy like disease in MT-ATP6 variant m.8969G>A
- 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
- Maculopapillary Bundle Degeneration in Optic Neuropathies
- 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
- MSC-mediated mitochondrial transfer restores mitochondrial DNA and function in neural progenitor cells 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
- Novel Mutations in the ND5 Gene Associated With Leber Hereditary Optic Neuropathy
- Optic Nerve T2 Signal Intensity and Caliber Reflect Clinical Severity in Genetic Optic Atrophy
- 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
- 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
- Preserved Ganglion Cell Analysis in a Case of Longstanding Leber Hereditary Optic Neuropathy: A Sign of Hibernating Neurons?
- Prevalence of Leber hereditary optic neuropathy in the Community of Madrid (Spain), estimation with a capture-recapture method
- 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
- Rare pathogenic nucleotide variants of mitochondrial DNA associated with Leber's hereditary 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