• A Homozygous NDUFS6 Variant Associated with Neuropathy and Optic Atrophy
• A Novel Grading System for Diffuse Chorioretinal Atrophy in Pathologic Myopia
• Age-related reductions in whole brain mass and telencephalon volume in very old white Carneau pigeons (Columba livia)
• Alpha-ketoglutaric acid attenuates oxidative stress and modulates mitochondrial dynamics and autophagy of spleen in a piglet model of lipopolysaccharide-induced sepsis
• An Algorithmic Approach to MR Imaging of Hypomyelinating Leukodystrophies
• An Italian case series' description of thiamine responsive megaloblastic anemia syndrome: importance of early diagnosis and treatment
• An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study
• An uncommon cause of optic atrophy in a young male
• Anterior Uveitis After Discontinuation of Janus Kinase Inhibitor, Ruxolitinib
• ARK5 enhances cell survival associated with mitochondrial morphological dynamics from fusion to fission in human multiple myeloma cells
• Assessment of retinal atrophy in mixed breed dogs using spectral domain optical coherence tomography (SD-OCT) and electroretinography
• Beyond Vision and Hearing: A Case Report of Wolfram Syndrome
• Biallelic BORCS8 variants cause an infantile-onset neurodegenerative disorder with altered lysosome dynamics
• Bilateral optic neuritis and encephalopathy as the atypical presentations of multiple sclerosis following severe acute respiratory syndrome coronavirus 2 infection
• Brain-Derived Neurotrophic Factor Val66Met is Associated with Variation in Cortical Structure in Healthy Aging Subjects
• Cardioprotective Action of a Novel Synthetic 19,20-EDP Analog Is Sirt Dependent
• Characteristics of myopic maculopathy in Chinese children and adolescents with high myopia
• Childhood-related neural genotype-phenotype in ATP1A3 mutations: comprehensive analysis
• Clinical Course and Visual Outcomes of Papilledema in Pediatric Cerebral Venous Sinus Thrombosis
• Clinical follow-up investigation on thickness changes in the peripapillary retinal nerve fibre layer of patients with Leber hereditary optic neuropathy
• Comprehensive overview of disease models for Wolfram syndrome: toward effective treatments
• Correlation between Residual Sensitivity in the Central Inferior Nasal Visual Field and Visual Function in Chronic Leber Hereditary Optic Neuropathy Patients
• Deep anterior lamellar keratoplasty and penetrating keratoplasty in macular corneal dystrophy: comparison of visual and topographic outcomes and complications
• Deep anterior lamellar keratoplasty and penetrating keratoplasty in macular corneal dystrophy: comparison of visual and topographic outcomes and complications
• Deep Learning-Enabled Vasculometry Depicts Phased Lesion Patterns in High Myopia Progression
• Development and validation of a deep learning model to predict axial length from ultra-wide field images
• Dihydromyricetin regulates RIPK3-CaMKII to prevent necroptosis in high glucose-stimulated cardiomyocytes
• Dose-Dependent Effects of Radiation on Mitochondrial Morphology and Clonogenic Cell Survival in Human Microvascular Endothelial Cells
• Downregulation of Mitochondrial Fusion Protein Expression Affords Protection from Canonical Necroptosis in H9c2 Cardiomyoblasts
• Dyskinetic Cerebral Palsy in Children: Clinical Perspectives on Common Comorbidities and Health-Related Quality of Life
• Electroacupuncture protects against cerebral ischemia-reperfusion injury through mitochondrial dynamics
• Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
• Endoscopic Optic Nerve Decompression in a Hamamy Syndrome Patient With Bilateral Optic Canal Stenosis
• Epiphora
• ER calcium depletion as a key driver for impaired ER-to-mitochondria calcium transfer and mitochondrial dysfunction in Wolfram syndrome
• Evaluation of Histopathologic Findings and Safety of Intravitreal Ketamine Administration on Vitreoretinal Tissue in Rat Model: A Pilot Study
• Expanding phenotype of MED13-associated syndrome presenting novel de novo missense variant in a patient with multiple congenital anomalies
• Exploring the evidence for mitochondrial dysfunction and genetic abnormalities in the etiopathogenesis of tropical ataxic neuropathy
• Fundus Tessellated Density of Pathologic Myopia
• Fundus Tessellation and Parapapillary Atrophy, as Ocular Characteristics of Spontaneously High Myopia in Macaques: The Non-Human Primates Eye Study
• Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy
• Giant 20/20 Meningioma: The Diagnostic Value of Confrontation Visual Fields
• High-Dose-Rate Yttrium-90 (⁹⁰Y) Episcleral Plaque Brachytherapy for Iris and Iridociliary Melanoma
• Infantile osteopetrosis with delayed development, organomegaly and wandering eyes: case report
• Infectious Scleritis - Clinical Characteristics, Causative Factors, and Treatment Outcomes in an Indian Population
• Inherited Optic Neuropathies: Real-World Experience in the Paediatric Neuro-Ophthalmology Clinic
• Leber hereditary optic neuropathy gene therapy
• Leber's hereditary optic neuropathy
• Long term clinical follow up of four patients with Wolfram syndrome and urodynamic abnormalities
• Long-term changes in morphological and functional parameters of the optic nerve in patients with various genetic variants of hereditary optic neuropathies
• Longitudinal optical coherence tomography indices in idiopathic intracranial hypertension
• Mitochondrial DNA mutations in Korean patients with Leber's hereditary optic neuropathy
• Mitochondrial F0F1-ATP synthase governs the induction of mitochondrial fission
• Multifaceted Roles of AFG3L2, a Mitochondrial ATPase in Relation to Neurological Disorders
• Mutation at the entrance of the quinone cavity severely disrupts quinone binding in respiratory complex I
• Mutations in NSUN3, a Mitochondrial Methyl Transferase Gene, Cause Inherited Optic Neuropathy
• Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-Associated Optic Neuritis - A Case Report and Literature Review
• Myopia and Other Refractive Error and Their Relationships to Glaucoma Screening
• Neuropathological hallmarks in the post-mortem retina of neurodegenerative diseases
• Ocular findings in Jansen metaphyseal chondrodysplasia
• Ocular manifestations in Koolen-de Vries syndrome: an international study
• Optic Atrophy From Retrograde Transsynaptic Axonal Degeneration Following Pediatric Brain Injury
• Optic Disc Drusen in Pseudoxanthoma Elasticum Are Associated with the Extent of Bruch's Membrane Calcification
• Optic Nerve T2 Signal Intensity and Caliber Reflect Clinical Severity in Genetic Optic Atrophy
• PallorMetrics: Software for Automatically Quantifying Optic Disc Pallor in Fundus Photographs, and Associations With Peripapillary RNFL Thickness
• Papillomacular bundle defect (PMBD) in glaucoma patients with high myopia: frequency and risk factors
• Parapapillary choroidal microvasculature dropout in eyes with primary open-angle glaucoma
• Peripapillary intrachoroidal cavitation at the crossroads of peripapillary myopic changes
• Phenotypic variability related to dominant UCHL1 mutations: about three families with optic atrophy and ataxia
• Phenotypic variation of FXN compound heterozygotes in a Friedreich ataxia cohort
• Posterior microphthalmos with retinal involvement related to <em>MFRP</em> gene: a report of 10 Brazilian patients
• Prenatal and Postnatal Ocular Abnormalities Following Congenital Zika Virus Infections: A Systematic Review
• Presentation of Ocular Syphilis with Bilateral Optic Neuropathy
• Preservation of orbit in tumor invasion through the periorbita in sinonasal malignancy
• Prevalence of blindness and visual impairment in a coastal region of Southern India: A cross-sectional survey in Prakasam district, Andhra Pradesh
• Prevalence of common and rare ophthalmic findings in adults attending a medical survey institute
• Prevalence of Leber hereditary optic neuropathy in the Community of Madrid (Spain), estimation with a capture-recapture method
• Prevalence, time course, and visual impact of peripapillary hyperreflective ovoid mass-like structures (PHOMS) in pediatric patients with optic nerve pathologies
• Prevalence, time course, and visual impact of peripapillary hyperreflective ovoid masslike structures (PHOMS) in pediatric patients with optic nerve pathologies
• Progression of Myopic Maculopathy Based on the ATN Classification System
• Real-world artificial intelligence-based interpretation of fundus imaging as part of an eyewear prescription renewal protocol
• Recurrent MECR R258W causes adult-onset optic atrophy: A case report
• Reduced FNDC5-AMPK signaling in diabetic atrium increases the susceptibility of atrial fibrillation by impairing mitochondrial dynamics and activating NLRP3 inflammasome
• Renal coloboma syndrome/dominant optic atrophy with severe retinal atrophy and de novo digenic mutations in PAX2 and OPA1
• Spastic Paraplegia Type 7-Associated Optic Neuropathy: A Case Series
• Surgical Outcomes of Revision Orbital Reconstruction in Patients With Inadequate Primary Orbital Fracture Repair
• Surgical outcomes of trigonal intraventricular meningiomas: a single-centre study
• Targeting DRP1 with Mdivi-1 to correct mitochondrial abnormalities in ADOA+ syndrome
• Tensile properties of glaucomatous human sclera, optic nerve, and optic nerve sheath
• The Effect of Cold-Water Swimming on Energy Metabolism, Dynamics, and Mitochondrial Biogenesis in the Muscles of Aging Rats
• The MOG antibody non-P42 epitope is predictive of a relapsing course in MOG antibody-associated disease
• The Wolfram-like variant WFS1^E864K destabilizes MAM and compromises autophagy and mitophagy in human and mice
• Therapeutic benefit of idebenone in patients with Leber hereditary optic neuropathy: The LEROS nonrandomized controlled trial
• Thiamine-Responsive Megaloblastic Anaemia With Hypothyroidism, A Puzzling Association
• Trans-Synaptic Degeneration in the Visual Pathway in Patients With Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease
• Trastuzumab-induced optic neuritis: "blindness" side effect
• Trends in Plasma Exchange Use in Optic Neuritis Hospitalizations in the United States
• Trends in Plasma Exchange Utilization in Optic Neuritis Hospitalizations in the United States
• TRPA1-PI3K/Akt-OPA1-ferroptosis axis in ozone-induced bronchial epithelial cell and lung injury
• Visual Agnosia Mimicking Memory Impairment: A Case Report of Posterior Cortical Atrophy