1. Editorial Board

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  2. Masthead

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  3. Table of Contents

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  4. EditorialWhat the American Journal of Ophthalmology Wants to Publish

    What the;Wants to Publish

  5. PerspectiveInternational Board Members of the American Journal of Ophthalmology

    This year marks the 100th anniversary of the “modern”;(AJO). International influence has been present since the beginnings of the journal, and the AJO had boasted a number of foreign editorial board members and collaborators over the years. Within the article we present sketches of the...

  6. Original articleCorneal Limbal Stem Cell Deficiency in Children with Stevens–Johnson Syndrome

    Of 19 children with SJS/TEN, LSCD developed in 6 (32%) patients at a mean of 12.3 ± 21.3 months after the onset of SJS/TEN (median 3.5 months). Severity of acute systemic involvement including elevation of liver enzyme levels and serum C-reactive protein levels was significantly correla...

  7. Original articleIncidence and Outcomes of Intraoperative Descemet Membrane Perforations During Deep Anterior Lamellar Keratoplasty

    Supplemental Material available at;.;Supplemental Material available at;.

  8. Original articleNear-Infrared Autofluorescence in Choroideremia: Anatomic and Functional Correlations

    All eyes could be categorized into 3 groups based on patterns of NIR-AF over the island of surviving retinal pigment epithelium: Group 1 (preserved NIR-AF centrally), Group 2 (only disrupted NIR-AF), or Group 3 (absence of NIR-AF). Group 1 eyes showed areas of NIR-AF that matched the areas...

  9. Original articleGlaucoma Specialist Detection of Optical Coherence Tomography Suspicious Rim Tissue in Glaucoma and Glaucoma Suspect Eyes

    Supplemental Material available at;.;Supplemental Material available at;.

  10. Original articleThe Natural History of Inherited Retinal Dystrophy Due to Biallelic Mutations in the RPE65 Gene

    To delineate the natural history of visual parameters over time in individuals with biallelic;mutation–associated inherited retinal dystrophy (IRD); describe the range of causative mutations; determine potential genotype/phenotype relationships; and describe the variety of clinical diagn...