1 - 10 of 43 articles
A woman in her 70s with a history of cutaneous melanoma presented with a pigmented iris lesion. Ultrasound biomicroscopy revealed a mid-low reflective anterior ciliochoroidal lesion centered in the nasal quadrant and extending circumferentially from the 12-o’clock position to the 7-o’clock...
Key PointsQuestionCan diagnostic criteria be defined for idiopathic orbital inflammation, which is a disorder diagnosed by exclusion?
FindingsUsing a modified Delphi consensus process, 35 international experts on orbital diseases agreed on a set of clinical and radiologic criteria for the...
Key PointsQuestionX-82 is an oral tyrosine kinase inhibitor that blocks the action of vascular endothelial growth factor and platelet-derived growth factor; might it treat neovascular age-related macular degeneration?
FindingsIn this phase 1 dose-escalation study of 35 participants, the most...
This case series provides detailed clinical, electrophysiologic, structural, and molecular genetic findings in nonsyndromic inherited retinal degenerations associated with CLN3 mutations.
This study investigates the susceptibilities of CoNS-causing endophthalmitis to fluoroquinolones over a 22-year time period at the Bascom Palmer Eye Institute, Miami, Florida, are reported.
A woman presented with bilateral decreased vision, bilateral hyperemic discs, macular edema, and subretinal fluid. What would you do next?
An infant born at 24 weeks’ gestation weighing 0.75 kg underwent examination with indirect ophthalmoscopy and scleral indentation for retinopathy of prematurity at 14 weeks’ postnatal age.
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