Search

Bispo, Paulo, Lawson Ung, James Chodosh, and Michael Gilmore. 2020. “Hospital-Associated Multidrug-Resistant MRSA Lineages Are Trophic to the Ocular Surface and Cause Severe Microbial Keratitis”. Front Public Health 8: 204.

Georgakopoulos, Constantinos, Foteini Tsapardoni, Olga Makri, and Demetrios Vavvas. 2022. “TWO-YEAR RESULTS OF INTRAVITREAL INJECTIONS OF AFLIBERCEPT IN COATS DISEASE: A CASE REPORT”. Retin Cases Brief Rep 16 (4): 473-78.

Xue, Yunlu, David Razafsky, Didier Hodzic, and Vladimir Kefalov. 2020. “Mislocalization of Cone Nuclei Impairs Cone Function in Mice”. FASEB J.

Hanekamp, Sandra, and Kristina Simonyan. 2020. “The Large-Scale Structural Connectome of Task-Specific Focal Dystonia”. Hum Brain Mapp.

Elhusseiny, Abdelrahman, Emery Jamerson, Rahma Menshawey, Emily Tam, and Yasmine El Sayed. 2020. “Collector Channels: Role and Evaluation in Schlemm’s Canal Surgery”. Curr Eye Res 45 (10): 1181-87.

Shu, Daisy, Erik Butcher, and Magali Saint-Geniez. 2020. “EMT and EndMT: Emerging Roles in Age-Related Macular Degeneration”. Int J Mol Sci 21 (12).

Ung, Lawson, Yvonne Wang, Mark Vangel, Emma Davies, Matthew Gardiner, Paulo Bispo, Michael Gilmore, and James Chodosh. 2020. “Validation of a Comprehensive Clinical Algorithm for the Assessment and Treatment of Microbial Keratitis”. Am J Ophthalmol 214: 97-109.

Jakobiec, Frederick, Mehenaz Hanbazazh, Paula Cortes Barrantes, and Michael Yoon. 2021. “Conjunctival Implantation Cyst in the Orbicularis Oculi Muscle: Review of a Possible Origin From Displaced Stem Cells With a Differential Diagnosis”. Ophthalmic Plast Reconstr Surg 37 (1): 1-11.

Orts-Vila, Paz, Francisco Amparo, José Luís Rodríguez-Prats, and Pedro Tañá-Rivero. 2020. “Alport Syndrome and Femtosecond Laser-Assisted Cataract Surgery”. J Ophthalmic Vis Res 15 (2): 264-69.

Furutani, Elissa, Ankoor Shah, Yongdong Zhao, David Andorsky, Fatma Dedeoglu, Amy Geddis, Yu Zhou, Towia Libermann, Kasiani Myers, and Akiko Shimamura. 2020. “Inflammatory Manifestations in Patients With Shwachman-Diamond Syndrome: A Novel Phenotype”. Am J Med Genet A 182 (7): 1754-60.