Ying and coauthors assess sustained visual acuity loss after 2 years of treatment with ranibizumab or bevacizumab for neovascular age-related macular degeneration.
Lin et al use a national health insurance database in Taiwan to determine contemporary estimates of the prevalence and incidence of sight-threatening diabetic retinopathy in patients with type 2 diabetes mellitus.
Birnbaum et al determine the correlation between symptoms and signs of disease activity in birdshot chorioretinopathy (BCR) and specific findings on optical coherence tomography with enhanced depth imaging (OCT-EDI).
Ghassemi et al describe the efficacy and complications of combined intravitreal chemotherapy, using melphalan and topotecan, for treatment of viable vitreous seeding from retinoblastoma.
Jia et al investigate the efficacy and safety of intralesional injection of pingyangmycin for treatment of low-flow orbital or periorbital venous malformations.
Dubey et al investigate the potential association of genetic variants across the LOXL1 gene in South Indian patients with pseudoexfoliation syndrome and glaucoma.
Zhang et al determine whether a single IOP measurement might adequately approximate the mean of several measurements in glaucoma surgical trials.
Shah and colleagues evaluate the oculomotor outcomes, anatomical changes, and complications associated with adjustable nasal transposition of the split lateral rectus muscle, a novel technique for managing strabismus associated with third nerve palsy.
Awadalla et al perform a clinical and genetic investigation of a large white family with autosomal dominant nanophthalmos.
He et al evaluate cohort effects and changes associated with aging in refractive errors among Chinese adults.
Uchino et al determine the relationship between mucin 5AC (MUC5AC) concentrations in the tears of visual display terminal users based on the diagnosis of dry eye disease and frequency of ocular symptoms.
Liu et al describe 3 cases of community-acquired methicillin-resistant Staphylococcus aureus (MRSA) acute dacryoadenitis.
Chandra et al describe the phenotypic characterization in newly reported patients with homozygous mutations in ADAMTS18 and report novel mutational data.
Siemiatkowska and coauthors describe mutation of the NMNAT1 gene in a subset of patients with Leber congenital amaurosis and macular atrophy.
McCannel et al report bilateral subfoveal neurosensory retinal detachments in 3 patients with metastatic cancer undergoing systemic therapy with MEK inhibitors.