Search Results - "Lin, Benjamin R"

7,8-dihydroxyflavone exhibits therapeutic efficacy in a mouse model of Rett syndrome by Johnson, Rebecca A, Lam, Maxine, Punzo, Antonio M, Li, Hongda, Lin, Benjamin R, Ye, Keqiang, Mitchell, Gordon S, Chang, Qiang

“…Rett syndrome (RTT), caused by mutations in the methyl-CpG binding protein 2 gene (MECP2), is a debilitating autism spectrum developmental disorder…”
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Transcriptomic Profiling of Posterior Polymorphous Corneal Dystrophy by Chung, Doug D, Frausto, Ricardo F, Lin, Benjamin R, Hanser, Evelyn M, Cohen, Zack, Aldave, Anthony J

“…To investigate the molecular basis of posterior polymorphous corneal dystrophy (PPCD) by examining the PPCD transcriptome and the effect of decreased ZEB1…”
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Self-Reported Perceptions of Preparedness among Incoming Ophthalmology Residents by Lin, Benjamin R, Nguyen, Geoffrey, Sridhar, Jayanth, Cavuoto, Kara

“…The purpose of this study was to assess the self-perceived preparedness of incoming postgraduate year 1 (PGY1) and postgraduate year 2 (PGY2) ophthalmology…”
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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 by Lin, Benjamin R, Le, Derek J, Chen, Yabin, Wang, Qiwei, Chung, D Doug, Frausto, Ricardo F, Croasdale, Christopher, Yee, Richard W, Hejtmancik, Fielding J, Aldave, Anthony J

“…To report identification of a COL17A1 mutation in a family with a corneal dystrophy previously mapped to chromosome 10q23-q24. Whole-exome sequencing was…”
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The ophthalmology residency match: a new era by Lin, Benjamin R., Sridhar, Jayanth, Uhler, Tara

“…The average number of applications per ophthalmology residency applicant continues to rise. The present article reviews the history and negative impacts of…”
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Identification of the First De Novo UBIAD1 Gene Mutation Associated with Schnyder Corneal Dystrophy by Chen, Judy L., Chiu, Stephan Y., Vo, Rosalind C., Frausto, Ricardo F., Lin, Benjamin R., Aldave, Anthony J.

“…Purpose. To report the identification of the first de novo UBIAD1 missense mutation in an individual with Schnyder corneal dystrophy (SCD). Methods. A slit…”
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Endophthalmitis Associated With XEN Stent Implantation by Lin, Benjamin R., Al-Khersan, Hasenin, Bitrian, Elena, Flynn, Harry W.

“…The aim of this study is to report the clinical characteristics, causative organisms, and treatment outcomes in patients presenting with endophthalmitis…”
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Reassessment of arterial versus venous perfusion of diabetic retinal neovascularization using ultrawide-field fluorescein angiography by Lin, Benjamin R, Carletti, Piero, Yi, Jonathan, Rosenfeld, Philip J, Russell, Jonathan F

“…The purpose of this study was to assess whether diabetic NV is perfused by the arterial or the venous circulation. This is a retrospective, consecutive case…”
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Clinical Outcomes after Ocular Trauma with Orbeez Gel Pellet Projectiles by Lin, Benjamin R., Al-Khersan, Hasenin, Rowsey, Tyler, West, Matthew, Lin, Albert, Qu, Phillip, Bitrian, Elena, Hudson, Julia, Venincasa, Michael, Fan, Jason, Gutkind, Naomi, Diaz, J. Daniel, Parekh, Prashant, Sultan, Harris, Yannuzzi, Nicolas A.

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Characterization of Retinal Lesions Secondary to Hemophagocytic Lymphohistiocytosis With OCTA by Lin, Benjamin R, Pluym, Ilina D, Tsui, Irena

“…Hemophagocytic lymphohistiocytosis (HLH) is a high-mortality primary immunologic or genetic disorder that rarely presents with ocular symptoms. This is a case…”
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Smith-Lemli-Optiz syndrome: importance of ophthalmology referral and follow-up by López-Cañizares, Ashley, Al-khersan, Hasenin, Fernandez, Maria P., Lin, Benjamin R., Goduni, Lediana, Berrocal, Audina M.

“…Smith-Lemli-Opitz syndrome (SLOS) is an autosomal recessive disorder caused by mutations in the 7-dehydrocholesterol reductase (DHCR7) gene, located on…”
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Coats-Like Presentation of Familial Exudative Vitreoretinopathy Associated With a Novel LRP5 Variant by López-Font, Francisco J, Shah, Serena M, Lin, Benjamin R, Cruz, Natasha Ferreira Santos da, Sengillo, Jesse D, Berrocal, Audina M

“…This report describes a unique case of a Coats-like presentation of familial exudative vitreoretinopathy in an 11-year-old girl. The patient was originally…”
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A Systematic Review of Acute Zonal Occult Outer Retinopathy with a Focus on Attempted Treatment Modalities by Lin, Benjamin R., Russell, Jonathan F., Al-Khersan, Hasenin, Goldhardt, Raquel

“…Acute zonal occult outer retinopathy (AZOOR) is a presumed inflammatory disorder leading to sectoral outer retinal dysfunction. This condition is characterized…”
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Investigating the Molecular Basis of PPCD3: Characterization of ZEB1 Regulation of COL4A3 Expression by Chung, Duk-Won D, Frausto, Ricardo F, Chiu, Stephan, Lin, Benjamin R, Aldave, Anthony J

“…To investigate the role of the zinc finger e-box binding homeobox 1 (ZEB1) transcription factor in posterior polymorphous corneal dystrophy 3 by demonstrating…”
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Relative Postpartum Retinal Vasoconstriction Detected With Optical Coherence Tomography Angiography by Lin, Benjamin R, Lin, Fei, Su, Li, Nassisi, Marco, Sadda, SriniVas R, Gaw, Stephanie L, Tsui, Irena

“…To characterize changes in retinal perfusion during pregnancy and the postpartum period using optical coherence tomography angiography (OCTA). A nonmydriatic…”
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Elucidating the molecular basis of PPCD: Effects of decreased ZEB1 expression on corneal endothelial cell function by Zakharevich, Marina, Kattan, Jaffer M, Chen, Judy L, Lin, Benjamin R, Cervantes, Aleck E, Chung, Doug D, Frausto, Ricardo F, Aldave, Anthony J

“…To investigate the functional role that the ( ) gene, which underlies the genetic basis of posterior polymorphous corneal dystrophy 3 (PPCD3), plays in corneal…”
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Student-Written Multiple-Choice Questions—a Practical and Educational Approach by Shah, Manan P., Lin, Benjamin R., Lee, Ming, Kahn, Daniel, Hernandez, Estebes

“…The purpose of our student-led project was to fulfill junior medical students’ demand for instructive, curriculum-specific practice questions while providing a…”
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Outcomes in Patients with Suprachoroidal Hemorrhage After Anterior Segment Surgery by Fan, Jason, Hudson, Julia L, Pakravan, Parastou, Lazzarini, Thomas A, Lin, Benjamin R, Fan, Kenneth C, Yannuzzi, Nicolas A, Sridhar, Jayanth, Townsend, Justin H, Berrocal, Audina M, Smiddy, William E, Vanner, Elizabeth A, Flynn, Jr, Harry W

“…The purpose of the current study is to report outcomes of suprachoroidal hemorrhage (SCH) after anterior segment surgery at a single institution, and to…”
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Maternal Optical Coherence Tomography Angiography Changes Related to Small for Gestational Age Pregnancies by Su, Li, Lin, Benjamin R, Lin, Fei, Tsui, Ilene K, Gaw, Stephanie L, Janzen, Carla, Sadda, SriniVas R, Tsui, Irena

“…To study maternal retinal changes in pregnancies that resulted in a small for gestational age (SGA) infant. Pregnant women with SGA infants at birth and…”
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Identification of presumed pathogenic KRT3 and KRT12 gene mutations associated with Meesmann corneal dystrophy by Chen, Judy L, Lin, Benjamin R, Gee, Katherine M, Gee, Jessica A, Chung, Duk-Won D, Frausto, Ricardo F, Deng, Sophie X, Aldave, Anthony J

“…To report potentially pathogenic mutations in the keratin 3 (KRT3) and keratin 12 (KRT12) genes in two individuals with clinically diagnosed Meesmann corneal…”
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