• 7,8,3'-Trihydroxyflavone prevents doxorubicin-induced cardiotoxicity and mitochondrial dysfunction via activating Akt signaling pathway in H9c2 cells
• A - 154 Neuropsychological Profile of a Patient Post Anoxic Brain Injury with Balint Syndrome: a Case Study Five Years Post-Injury
• A family with Charcot-Marie-Tooth disease and Leber's optic atrophy
• A novel stop-gain <em>NF1</em> variant in neurofibromatosis type 1 and bilateral optic atrophy without optic gliomas
• A Retrospective Cohort Study on the Difficulties of Diagnosing and Managing Glaucoma in Patients with Coexistent Neurodegenerative Disease
• Advanced Optical Microscopy: Unveiling Functional Insights Regarding a Novel <em>PPP2R1A</em> Variant and Its Unreported Phenotype
• Approaches to the epidemiology of NOHL in the region of Madrid: Survey of neuro-ophthalmologists
• Association between optic atrophy 1 polymorphisms and primary open angle glaucoma risk: Based on a meta-analysis
• Attenuation of PM_2.5-induced alveolar epithelial cells and lung injury through regulation of mitochondrial fission and fusion
• Autosomal recessive pathogenic MSTO1 variants in hereditary optic atrophy
• Binasal Field Defect in Non-arteritic Anterior Ischemic Optic Neuropathy
• Characteristics of the Peripapillary Structure and Vasculature in Patients With Myopic Anisometropia
• Charles Bonnet syndrome in an elderly blind man with recurrent pituitary macroadenoma and optic nerve atrophy: A case report
• Clinical, radiological, biochemical and molecular characterization of a new case with multiple mitochondrial dysfunction syndrome due to IBA57: Lysine and tryptophan metabolites as potential biomarkers
• Diagnostic Yield of Investigations in Symmetric Optic Neuropathy
• Distribution of the retinal microcirculation based on the morphology of peripapillary atrophy in high myopia
• Down-regulation of the mitochondrial fusion protein Opa1/Mfn2 promotes cardiomyocyte hypertrophy in Su5416/hypoxia-induced pulmonary hypertension rats
• Dural venous sinus stenting technique for idiopathic intracranial hypertension in patients with tortuous venous anatomy
• Early-onset Myopia and Retinal Detachment without Typical Microcoria or Severe Proteinuria due to a Novel LAMB2 Variant
• Effects of Lactiplantibacillus plantarum on oxidative stress, mitophagy, and NLRP3 inflammasome activation in broiler breast meat
• Efficacy and safety of avacincaptad pegol in patients with geographic atrophy (GATHER2): 12-month results from a randomised, double-masked, phase 3 trial
• Epiphora
• Eye lesions and onchocerciasis in a rural farm settlement in Delta state, Nigeria
• Eye Lesions in Patients After One Year of Kidney Transplantation
• Fatty acid β-oxidation and mitochondrial fusion are involved in cardiac microvascular endothelial cell protection induced by glucagon receptor antagonism in diabetic mice
• Flt3 Activation Mitigates Mitochondrial Fragmentation and Heart Dysfunction through Rebalanced L-OPA1 Processing by Hindering the Interaction between Acetylated p53 and PHB2 in Cardiac Remodeling
• Genetic basis of hereditary optic atrophies
• GM3 Synthase Deficiency
• High-fat diet causes mitochondrial damage and downregulation of mitofusin-2 and optic atrophy-1 in multiple organs
• Inborn errors of biotin metabolism. Clinical and laboratory features of eight cases
• Incidence of blindness in southern Germany due to glaucoma and degenerative conditions
• Interactions of optic radiation lesions with retinal and brain atrophy in early multiple sclerosis
• Irisin protects against doxorubicin-induced cardiotoxicity by improving AMPK-Nrf2 dependent mitochondrial fusion and strengthening endogenous anti-oxidant defense mechanisms
• Knock-down of ROCK2 gene improves cognitive function and reduces neuronal apoptosis in AD mice by promoting mitochondrial fusion and inhibiting its division
• Long noncoding RNA H19 promotes vascular calcification by repressing the Bax inhibitor 1/optic atrophy 1 pathway
• Long-term follow-up of severe autosomal recessive SP7-related bone disorder
• Loss and recovery of myocardial mitochondria in mice under different tail suspension time: Apoptosis and mitochondrial fission, fusion and autophagy
• Management of retinal detachment due to closed globe injury by pars plana vitrectomy with and without scleral buckling
• Modeling MOG Antibody-Associated Disorder and Neuromyelitis Optica Spectrum Disorder in Animal Models: Visual System Manifestations
• Monocular blindness in Bayelsa state of Nigeria
• More extensive structural damage in temporal lobe epilepsy with hippocampal sclerosis type 1
• Natural History of Untreated Optic Neuritis Associated With Mild COVID-19 Infection
• Neurosyphilis: 53 cases
• New retinal findings in NLRP3-associated autoinflammatory disease
• New therapeutic directions in type II diabetes and its complications: mitochondrial dynamics
• Next generation sequencing identifies a pathogenic mutation of WFS1 gene in a Moroccan family with Wolfram syndrome: a case report
• Ocular manifestations following COVID-19 vaccination
• OPA1 helical structures give perspective to mitochondrial dysfunction
• Outcomes of vitreoretinal surgery in patients with closed-globe injury
• Papilledema in the setting of x-linked hypophosphatemic rickets with craniosynostosis
• Performance of neuroretinal rim thickness measurement by Cirrus high-definition optical coherence tomography in myopic eyes
• PLAAT1 expression triggers fragmentation of mitochondria in an enzyme activity-dependent manner
• Prevalence and Associations of Non-Glaucomatous Optic Nerve Atrophy in High Myopia. The Ural Eye and Medical Study
• Prevalence and Cause of Loss of Visual Acuity and Visual Field in Highly Myopic Eyes. The Beijing Eye Study
• Prevalence and Risk Factors of Fundus Pathology in Patients with Type 2 Diabetes in a Northeastern Chinese Cohort
• Prevalence of blindness and visual impairment in a coastal region of Southern India: A cross-sectional survey in Prakasam district, Andhra Pradesh
• Prevalence of propionic acidemia in China
• Protective effects of Shen Yuan Dan on myocardial ischemia-reperfusion injury via the regulation of mitochondrial quality control
• Quantitative Anterior Chamber Drainage and its Relationship with Initial Intraocular Pressure in Ocular Hypertension: A Comparative Study
• Quantization of Optic Disc Characteristics in Young Adults Based on Artificial Intelligence
• Recessive <em>MECR</em> pathogenic variants cause an LHON-like optic neuropathy
• Saponins from <em>Panax japonicus</em> improve neuronal mitochondrial injury of aging rats
• SIRT4 is a regulator of human skeletal muscle fatty acid metabolism influencing inner and outer mitochondrial membrane-mediated fusion
• SIRT4 is a regulator of human skeletal muscle fatty acid metabolism influencing inner and outer mitochondrial-mediated fusion
• Spastic paraplegia, optic atrophy, and neuropathy is linked to chromosome 11q13
• Spastic paraplegia, optic atrophy, and neuropathy: new observations, locus refinement, and exclusion of candidate genes
• SPECT/CT imaging for tracking subendothelial retention of electronegative low-density lipoprotein in vivo
• Sustained OMA1-mediated integrated stress response is beneficial for spastic ataxia type 5
• Swelling of Atrophic Optic Discs in Idiopathic Intracranial Hypertension
• Temporal Optic Disc Microvasculature Dropout in Glaucoma
• The miR-668 binding site variant rs1046322 on <em>WFS1</em> is associated with obesity in Southeast Asians
• The optic disc in Leber congenital amaurosis
• The Role of Mitochondrial Dynamics and Mitotic Fission in Regulating the Cell Cycle in Cancer and Pulmonary Arterial Hypertension: <em>Implications for Dynamin-Related Protein 1 and Mitofusin2 in Hyperproliferative Diseases</em>
• The Role of Swelling in the Regulation of OPA1-Mediated Mitochondrial Function in the Heart In Vitro
• Trimodality optical imaging for tracking subendothelial retention of electronegative low-density lipoprotein in vivo
• TRPA1 promotes cisplatin-induced acute kidney injury via regulating the endoplasmic reticulum stress-mitochondrial damage
• Variants in the WDR45 Gene Within the OPA-2 Locus Associate With Isolated X-Linked Optic Atrophy
• Wolfram Syndrome 1 in Two Brothers Treated with Insulin Pump
• Wolfram syndrome 1 regulates sleep in dopamine receptor neurons by modulating calcium homeostasis
• Wolfram Syndrome-2, a Cause of Severe Gastrointestinal Bleeding: A Case Series and a Literature Review
• Α rare case of myopathy, lactic acidosis, and severe rhabdomyolysis, due to a homozygous mutation of the ferredoxin-2 (FDX2) gene
• α-Synuclein pathology in post-mortem retina and optic nerve is specific for α-synucleinopathies