Disease: Optic atrophy 2
- 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<sub>2.5</sub>-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