Proteolytic activity in the meibomian gland: Implications to health and disease
Argüeso, Pablo. 2017. “Proteolytic Activity in the Meibomian Gland: Implications to Health and Disease”. Exp Eye Res 163: 53-57.
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The Mystery of the Locking Eye
Bouffard, Marc, and Nurhan Torun. 2017. “The Mystery of the Locking Eye”. JAMA Neurol 74 (5): 601-2.
Pathogenic Role of MicroRNA-21 in Diabetic Retinopathy Through Down-Regulation of PPARα
Chen, Qian, Fangfang Qiu, Kelu Zhou, Greg Matlock, Yusuke Takahashi, Raju Rajala, Yanhui Yang, Elizabeth Moran, and Jian-Xing Ma. 2017. “Pathogenic Role of MicroRNA-21 in Diabetic Retinopathy Through Down-Regulation of PPARα”. Diabetes.
Reply re: Dr. Kubota's Letter to the Editor, "Corticosteroids or biopsy for idiopathic orbital inflammation"
Dagi Glass, Lora, and Suzanne Freitag. 2017. “Reply Re: Dr. Kubota’s Letter to the Editor, ‘Corticosteroids or Biopsy for Idiopathic Orbital Inflammation’”. Surv Ophthalmol 62 (2): 255.
A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts
Lindström, Sara, Stephanie Loomis, Constance Turman, Hongyan Huang, Jinyan Huang, Hugues Aschard, Andrew Chan, et al. 2017. “A Comprehensive Survey of Genetic Variation in 20,691 Subjects from Four Large Cohorts”. PLoS One 12 (3): e0173997.
A Young Woman With Headaches and Blurry Vision
Scott, Nathan, Tomasz Stryjewski, and Joseph Rizzo. 2017. “A Young Woman With Headaches and Blurry Vision”. JAMA Ophthalmol 135 (6): 663-64.
Risk of Ocular Hypertension in Adults with Noninfectious Uveitis
Daniel, Ebenezer, Maxwell Pistilli, Srishti Kothari, Naira Khachatryan, Oktay Kaçmaz, Sapna Gangaputra, Nida Sen, et al. 2017. “Risk of Ocular Hypertension in Adults With Noninfectious Uveitis”. Ophthalmology 124 (8): 1196-1208.
Combined Central Retinal Vein Occlusion and Central Retinal Arterial Obstruction with Cilioretinal Artery Sparing
Gaier, Eric, John Miller, and John Loewenstein. 2017. “Combined Central Retinal Vein Occlusion and Central Retinal Arterial Obstruction With Cilioretinal Artery Sparing”. Ophthalmology 124 (4): 576.
Biallelic mutations in human DCC cause developmental split-brain syndrome
Jamuar, Saumya, Klaus Schmitz-Abe, Alissa D’Gama, Marie Drottar, Wai-Man Chan, Maya Peeva, Sarah Servattalab, et al. 2017. “Biallelic Mutations in Human DCC Cause Developmental Split-Brain Syndrome”. Nat Genet 49 (4): 606-12.
Identification of RUNX1 as a Mediator of Aberrant Retinal Angiogenesis
Lam, Jonathan, Daniel Oh, Lindsay Wong, Dhanesh Amarnani, Cindy Park-Windhol, Angie Sanchez, Jonathan Cardona-Velez, et al. 2017. “Identification of RUNX1 As a Mediator of Aberrant Retinal Angiogenesis”. Diabetes 66 (7): 1950-56.