All Stories

  1. CRX-linked macular dystrophy with intrafamilial variable expressivity
  2. EXTRAMACULAR FIBROSIS IN COATSʼ DISEASE
  3. Swiss Family with Dominant Stargardt Disease Caused by a Recurrent Mutation in the ELOVL4 Gene
  4. Presence of a Triple Concentric Autofluorescence Ring inNR2E3-p.G56R–Linked Autosomal Dominant Retinitis Pigmentosa (ADRP)
  5. Differential Dimerization of Variants Linked to Enhanced S-Cone Sensitivity Syndrome (ESCS) Located in the NR2E3 Ligand-Binding Domain
  6. PATTERN DYSTROPHY WITH HIGH INTRAFAMILIAL VARIABILITY ASSOCIATED WITH Y141C MUTATION IN THE PERIPHERIN/RDS GENE AND SUCCESSFUL TREATMENT OF SUBFOVEAL CNV RELATED TO MULTIFOCAL PATTERN TYPE WITH ANTI-VEGF (RANIBIZUMAB) INTRAVITREAL INJECTIONS
  7. Double Concentric Autofluorescence Ring in NR2E3 -p.G56R-Linked Autosomal Dominant Retinitis Pigmentosa
  8. Leber Congenital Amaurosis Associated with AIPL1: Challenges in Ascribing Disease Causation, Clinical Findings, and Implications for Gene Therapy
  9. Angioid streaks with severe macular dysfunction and generalised retinal involvement due to a homozygous duplication in the ABCC6 gene
  10. Risk assessment of recurrence in sporadic retinoblastoma using a molecular-based algorithm
  11. Persistence of Increased Eotaxin-1 (CCL11) Level in Tears of Patients Wearing Contact Lenses: A Long-Term Follow-Up Study
  12. Therapeutic Strategies for Nonendemic Onchocerciasis
  13. Uvéites médicamenteuses - Panuvéite sur RifabutinDrug-induced uveitis - panuveitis with Rifabutin
  14. In vivo study comparing an X-shaped polymethylmethacrylate and a cylindrical collagen implant for deep sclerectomy
  15. Comparing Deep Sclerectomy With Collagen Implant With the New Method of Very Deep Sclerectomy With Collagen Implant
  16. Comparing Deep Sclerectomy With Collagen Implant to the New Method of Very Deep Sclerectomy With Collagen Implant
  17. Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors
  18. Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors
  19. Ultrasound biomicroscopic assessment of zonular appearance in exfoliation syndrome
  20. BILATERAL CIRCUMSCRIBED CHOROIDAL HEMANGIOMA IN AN OTHERWISE HEALTHY INDIVIDUAL
  21. Evanescent White Linear Flecks and Posterior Microphthalmos: New Features of a Recently Established Disease
  22. Blood-Brain Barrier Disruption Associated with Topiramate-Induced Angle-Closure Glaucoma of Acute Onset
  23. Peripapillary choroidal neovascularization associated with melanocytoma of the optic disc: a clinicopathologic case report
  24. Primary Choroidal Melanoma in Phakomatosis Pigmentovascularis IIa
  25. Iridociliary apposition in plateau iris syndrome persists after cataract extraction
  26. High-Frequency Ultrasonographic Evaluation of Conjunctival Intraepithelial Neoplasia and Squamous Cell Carcinoma
  27. Ultrasound biomicroscopy in uveitis-glaucoma- hyphema syndrome
  28. Angle closure: classification, concepts, and the role of ultrasound biomicroscopy in diagnosis and treatment