• A case of Axenfeld-Rieger syndrome with retinal detachment
• A rare case of bilateral granular corneal dystrophy with keratoconus and primary angle closure glaucoma
• A rare case of unilateral Axenfeld-Rieger anomaly associated with optic disc coloboma: A multimodal imaging canvas
• Adams-Oliver syndrome associated with refractory glaucoma
• Adeno-associated virus mediated gene therapy for neuroprotection of retinal ganglion cells in glaucoma
• Allele and genotype frequencies for primary hereditary cataract, multifocal retinopathy 1, and degenerative myelopathy in Pyrenean Mountain dog from Italy
• Anatomical and morphometric features of anterior eye segment structures in hyperopia and the risk of developing primary angle-closure glaucoma
• Angle-closure glaucoma associated with autosomal recessive bestrophinopathy
• Applying the 2022 optic neuritis criteria to noninflammatory optic neuropathies with optic nerve T2-hyperintensity: an observational study
• Association between retinitis pigmentosa and an increased risk of primary angle closure glaucoma: A population-based cohort study
• Autofluorescence Imaging to Evaluate Retinal Disease Progression in Rodent
• Axenfeld-Rieger syndrome: more than meets the eye
• Bilateral Progressive Optic Neuropathy in a Patient with Familial Amyloid Polyneuropathy: Amyloid Deposits in the Optic Nerve Head?
• Can Nerve Growth Factor (NGF) Be a Treatment Option for Pediatric Eye Diseases?
• Cardiac anomalies in Axenfeld-Rieger syndrome
• Case Report: An Unusual Presentation of Leber's Hereditary Optic Neuropathy
• Characteristics of beta parapapillary atrophy in primary angle-closure suspect
• Childhood Glaucoma
• Chromatic pupillometry for evaluating melanopsin retinal ganglion cell function in Alzheimer's disease and other neurodegenerative disorders: a review
• Classic anterior lenticonus in Alport syndrome
• Clinical and diagnostic imaging profile of three anterior segment dysgenesis disorders presenting with infantile corneal opacities
• Clinical and genetic features in autosomal recessive bestrophinopathy in Chinese cohort
• Clinical exome sequencing for inherited retinal degenerations at a tertiary care center
• Clinical Features and Genetic Findings of Autosomal Recessive Bestrophinopathy
• Clinical features of retinal amyloid angiopathy with transthyretin Gly83Arg variant
• Commercial Gene Panels for Congenital Anterior Segment Anomalies: Are They All the Same?
• Comparing Gene Panels for Non-Retinal Indications: A Systematic Review
• Comparison of Anterior Segment Abnormalities in Individuals With FOXC1 and PITX2 Variants
• Complete detachment of the Schwalbe's line in a case of Axenfeld-Reiger anomaly - A rare presentation
• Complications in deep anterior lamellar keratoplasty - A retrospective interventional analysis in a large series
• CRISPR editing of anti-anemia drug target rescues independent preclinical models of retinitis pigmentosa
• Cross-sectional observational analysis of the genetic referral practices across pediatric ophthalmology outpatient departments in an urban setting
• Current management of infantile cataracts
• 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
• Distal renal tubular acidosis, autoimmune thyroiditis, enamel hypomaturation, and tooth agenesis caused by homozygosity of a novel double-nucleotide substitution in SLC4A4
• Distribution of TGFBI variants in patients with early onset glaucoma
• DNA Damage and Repair in Eye Diseases
• Does Patisiran Reduce Ocular Transthyretin Synthesis? A Pilot Study of Two Cases
• Effects of optic nerve head-related parameters on retinal vessel calibers measurement results on fundus photographs
• Efficacy of Continuous-Wave Transscleral Cyclophotocoagulation Post-Pars Plana Vitrectomy in Glaucoma Patients: A Retrospective Study from Poland
• Eserine, in Crooked House and Curtain
• Exome Sequencing Reveals <em>SLC4A11</em> Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
• Exome Sequencing Reveals SLC4A11 Variant Underlying Congenital Hereditary Endothelial Dystrophy (CHED2) Misdiagnosed as Congenital Glaucoma
• Extranuclear DNA Variations in the Susceptibility of Glaucoma
• Foveolar thickness as potential standardized structural outcome measurement in studies of Bietti crystalline dystrophy
• Fuchs Uveitis Syndrome
• Fuchs Uveitis Syndrome
• Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome
• In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome
• Injectable, Antioxidative, and Tissue-Adhesive Nanocomposite Hydrogel as a Potential Treatment for Inner Retina Injuries
• Japan to Global Eye Genetics Consortium: Extending Research Collaboration for Inherited Eye Diseases
• Japan to Global Eye Genetics Consortium: Extending Research Collaboration for Inherited Eye Diseases
• Juvenile Glaucoma
• Letter to the editor on: prophylactic nicotinamide treatment protects from rotenone-induced neurodegeneration by increasing mitochondrial content and volume
• Long-term risk of glaucoma after cataract surgery in childhood
• Long-term surgical results of trabeculectomy for secondary glaucoma in Val30Met hereditary transthyretin amyloidosis
• Long-term visual outcomes and ocular complications in children with Marner's hereditary cataracts operated in the period 1940-2021
• Maculopapillary Bundle Degeneration in Optic Neuropathies
• Managing a rare case of familial Radius Maumenee syndrome
• Megalocornea
• Megalocornea
• Microhook ab interno trabeculotomy for secondary glaucoma in patients with hereditary transthyretin amyloidosis
• Modified Technique of Ex-PRESS() Filtration Device Combined with a Scleral Pocket for Hereditary Transthyretin Amyloidosis (hATTR) Secondary Open-Angle Glaucoma
• Modified Technique of Ex-PRESS^® Filtration Device Combined with a Scleral Pocket for Hereditary Transthyretin Amyloidosis (hATTR) Secondary Open-Angle Glaucoma
• Multiocular defect in the Old English Sheepdog: A canine form of Stickler syndrome type II associated with a missense variant in the collagen-type gene COL11A1
• Neurotrophic Keratopathy After Slow Coagulation Transscleral Cyclophotocoagulation
• Ophthalmological involvement in wild-type transthyretin amyloidosis: A multimodal imaging study
• Optic nerve diseases and regeneration: How far are we from the promised land?
• Optical Coherence Tomography
• Optical coherence tomography findings in three patients with Werner syndrome
• Optimisation of AAV-NDI1 Significantly Enhances Its Therapeutic Value for Correcting Retinal Mitochondrial Dysfunction
• Oxidative Stress: A Suitable Therapeutic Target for Optic Nerve Diseases?
• Pars-plana vitrectomy for the treatment of vitreous amyloid in patients with hereditary transthyretin amyloidosis
• Participation of Lens Proteins and miRs in Traumatic and Inheritance Cataract: A Review on Diagnostic and Therapeutic Approaches for Cataract Management
• Patients with Retinitis Pigmentosa May Have a Higher Risk of Developing Open-Angle Glaucoma
• Pediatric Cataract
• Pigment dispersion syndrome and pigmentary glaucoma: overview and racial disparities
• Pigmented paravenous retinochoroidal atrophy with acute angle-closure glaucoma and posterior subcapsular cataract: a case report
• Poor intraoperative visibility and postoperative astigmatism associated with trabecular micro-bypass stent for corneal dystrophy: A case report
• Posterior Polymorphous Corneal Dystrophy
• Posterior Polymorphous Corneal Dystrophy
• Pyrroloquinoline quinone drives ATP synthesis in vitro and in vivo and provides retinal ganglion cell neuroprotection
• Research progress of iron metabolism in retinal diseases
• Retinal Vascular Anomalies (VHL, Cavernous Hemangioma, Wyburn-Mason)
• Secondary open-angle pigmentary glaucoma resulting from a single-piece hydrophobic intraocular lens in the sulcus
• Severe Dry Eye Disease in Charcot-Marie-Tooth Disease: A Comprehensive Case Report
• Short-Wavelength Light-Blocking Filters and Oral Melatonin Administration in Patients With Retinitis Pigmentosa: Protocol for a Randomized Controlled Trial
• Suture trabeculotomy ab interno for secondary glaucoma in Japanese patients with Val30Met hereditary transthyretin amyloidosis
• The Potential and Application of iPSCs in Gene and Cell Therapy for Retinopathies and Optic Neuropathies
• The potential of stem cell therapy to tackle visual impairment
• The Prevalence of Cataract in Children
• The Role of the Disrupted Podosome Adaptor Protein (SH3PXD2B) in Frank-Ter Haar Syndrome
• The Significance of Screening Family Members in Glaucoma: Opportunities and Challenges
• Topical Losartan: Practical Guidance for Clinical Trials in the Prevention and Treatment of Corneal Scarring Fibrosis and Other Eye Diseases and Disorders
• Truncation mutations in MYRF underlie primary angle closure glaucoma
• Vitreoretinopathy-Associated Pediatric Retinal Detachment Treatment Outcomes: IRIS® Registry (Intelligent Research in Sight) Analysis
• Vogt-Koyanagi-Harada Syndrome: A Case Report
• Von Hippel-Lindau Syndrome
• Von Hippel-Lindau Syndrome