6 hasil untuk "Benjamin R. Lin"

Self-Reported Perceptions of Preparedness among Incoming Ophthalmology Residents

Benjamin R. Lin; Geoffrey Nguyen; Jayanth Sridhar dkk.

Journal of Academic Ophthalmology, Vol. 15 No. 02 · 2023 · Inggris · DOAJ

Purpose The purpose of this study was to assess the self-perceived preparedness of incoming postgraduate year 1 (PGY1) and postgraduate year 2 (PGY2) ophthalmology interns/residents to carry out core competencies in ophthalmology.

Fovea Sparing Branch Retinal Artery Occlusions Imaged with Optical Coherence Tomography Angiography: Two Case Reports

Benjamin R. Lin; Philip J. Rosenfeld; Harry W. Flynn Jr.

Case Reports in Ophthalmology, Vol. 16 No. 1 · 2025 · Inggris · DOAJ Scopus

Introduction: Central retinal artery occlusions and branch retinal artery occlusions (BRAOs) are ophthalmic emergencies that require workups for systemic risk factors. In the acute setting, BRAOs present with retinal whitening in a sectoral pattern on exam as well as hyperreflectivity and…

Maculopathy after long-term use of fondaparinux, a heparin mimetic and heparanase inhibitor

Benjamin R. Lin; Erick Rivera-Grana; Wenting Zhou dkk.

American Journal of Ophthalmology Case Reports, Vol. 38 · 2025 · Inggris · DOAJ Scopus

Purpose: To report maculopathy associated with the long-term use of fondaparinux, a heparin mimetic and inhibitor of the extracellular matrix enzyme, heparanase. Observations: A 41-year-old woman receiving thrice weekly injections of fondaparinux as prophylaxis against deep vein thrombosis for 9…

Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy

Benjamin R. Lin; Ricardo F. Frausto; Rosalind C. Vo dkk.

Journal of Ophthalmology, Vol. 2016 · 2016 · Inggris · DOAJ Scopus

Purpose. To report the identification of the first de novo UBIAD1 missense mutation in an individual with Schnyder corneal dystrophy (SCD). Methods. A slit lamp examination was performed on a 47-year-old woman without a family history of corneal disorders. The proband’s parents, two sisters, and…

Whole Exome Sequencing and Segregation Analysis Confirms That a Mutation in COL17A1 Is the Cause of Epithelial Recurrent Erosion Dystrophy in a Large Dominant Pedigree Previously Mapped to Chromosome 10q23-q24

Benjamin R. Lin; Derek J. Le; Yabin Chen dkk.

PLOS ONE, Vol. 11 No. 6 · 2016 · Inggris · PLOS Scopus

Purpose: To report identification of a COL17A1 mutation in a family with a corneal dystrophy previously mapped to chromosome 10q23-q24. Methods: Whole-exome sequencing was performed on DNA samples from five affected family members and two unrelated, unaffected individuals. Identified variants were…

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