PubMed ID: 37975905 Author(s): Williams BN, Draper A, Lang PF, Lewis TR, Smith AL, Mayerl SJ, Rougie M, Simon JM, Arshavsky VY, Greenwald SH, Gamm DM, Pinilla I, Philpot BD. Heterogeneity in the progression of …
Publications
Regional variation in the organization and connectivity of the first synapse in the primate night vision pathway.
PubMed ID: 37915604 Author(s): Saha A, Zuniga J, Mian K, Zhai H, Derr PJ, Hoon M, Sinha R. Regional variation in the organization and connectivity of the first synapse in the primate night vision pathway. …
Intraocular Pressure in Eyes With Retinal Vein Occlusion Compared With Fellow Eyes: Study of Comparative Treatments for Retinal Vein Occlusion 2 (SCORE2) Report 27.
PubMed ID: 37943541 Author(s): Aref AA, Scott IU, Oden NL, Ip MS, VanVeldhuisen PC, Blodi BA; SCORE and SCORE2 Study Investigator Groups. Intraocular Pressure in Eyes With Retinal Vein Occlusion Compared With Fellow Eyes: Study …
Structural and Functional Changes in Non-Paraneoplastic Autoimmune Retinopathy.
PubMed ID: 37958272 Author(s): Akhavanrezayat A, Khatri A, Onghanseng NGL, Halim MS, Or C, Sredar N, Razeen M, Hasanreisoglu M, Regenold J, Thng ZX, Mohammadi SS, Jain T, Yavari N, Bazojoo V, Gupta AS, Mobasserian …
Construction of an Exudative Age-Related Macular Degeneration Diagnostic and Therapeutic Molecular Network Using Multi-Layer Network Analysis, a Fuzzy Logic Model, and Deep Learning Techniques: Are Retinal and Brain Neurodegenerative Disorders Related?
PubMed ID: 38004422 Author(s): Latifi-Navid H, Barzegar Behrooz A, Jamehdor S, Davari M, Latifinavid M, Zolfaghari N, Piroozmand S, Taghizadeh S, Bourbour M, Shemshaki G, Latifi-Navid S, Arab SS, Soheili ZS, Ahmadieh H, Sheibani N. …
A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family.
PubMed ID: 37854028 Author(s): Chen Y, Kellom ER. A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family. Am J Ophthalmol Case Rep. 2023 Oct 5;32:101936. doi: 10.1016/j.ajoc.2023.101936. …
A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family.
PubMed ID: 37854028 Author(s): Chen Y, Kellom ER. A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family. Am J Ophthalmol Case Rep. 2023 Oct 5;32:101936. doi: 10.1016/j.ajoc.2023.101936. …
A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family.
PubMed ID: 37854028 Author(s): Chen Y, Kellom ER. A rare, likely pathogenic variant causing Leber’s hereditary optic neuropathy in three-generation females of an African-American family. Am J Ophthalmol Case Rep. 2023 Oct 5;32:101936. doi: 10.1016/j.ajoc.2023.101936. …
Contralateral Astrocyte Response to Acute Optic Nerve Damage Is Mitigated by PANX1 Channel Activity.
PubMed ID: 37958624 Author(s): Wurl JA, Mac Nair CE, Dietz JA, Shestopalov VI, Nickells RW. Contralateral Astrocyte Response to Acute Optic Nerve Damage Is Mitigated by PANX1 Channel Activity. Int J Mol Sci. 2023 Oct …