To identify the gene or genes responsible for developmental causes of blindness in the world, and to establish a Pediatric Ophthalmic Genetics and Research Program at the University of Wisconsin–Madison.
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XOLARIS
To gain a better understanding of disease progression over time in male subjects with X-linked retinitis pigmentosa (XLRP).
CHM SURVEY TRIAL
Choroideremia (CHM) Health Outcomes
CATALINA
A Phase II Multicenter, Randomized, Double-Masked, Sham-Controlled Study of the Safety and Efficacy of Intravitreal Injections of NGM621 in Subjects with Geographic Atrophy (GA) Secondary to Age-Related Macular Degeneration (AMD) (CATALINA)
DOVS Mentee Presents at Medical Student Research Forum
Claire Vanden Heuvel, a second-year medical student and mentee in the Julie Mares Laboratory, presented a poster at the 19th Annual Medical Student Research Forum on November 23. Her project, the culmination of work during …
Two cases of epidemic keratoconjunctivitis-associated dacryocystitis.
PubMed ID: 31852315 Author(s): Vo KBH, Lucarelli MJ, van Landingham SW. Two cases of epidemic keratoconjunctivitis-associated dacryocystitis. Orbit. 2020 Dec;39(6):450-453. doi: 10.1080/01676830.2019.1705499. Epub 2019 Dec 18. PMID 31852315 Journal: Orbit (Amsterdam, Netherlands), Volume 39, Issue …
Deep Learning Automated Detection of Reticular Pseudodrusen from Fundus Autofluorescence Images or Color Fundus Photographs in AREDS2.
PubMed ID: 32447042 Author(s): Keenan TDL, Chen Q, Peng Y, Domalpally A, Agrón E, Hwang CK, Thavikulwat AT, Lee DH, Li D, Wong WT, Lu Z, Chew EY. Deep learning automated detection of reticular pseudodrusen …
Necrotizing myositis in a rectus muscle arising in the setting of long-standing Langerhans cell histiocystosis and recent dabrafenib treatment.
PubMed ID: 32875153 Author(s): van Landingham SW, Puccetti D, Potter H, Gamm D, Diamond EL, Lucarelli MJ. Necrotizing myositis in a rectus muscle arising in the setting of long-standing Langerhans cell histiocystosis and recent dabrafenib …
Ocular evaluation and genetic test for an early Alström Syndrome diagnosis.
PubMed ID: 32944671 Author(s): Etheridge T, Kellom ER, Sullivan R, Ver Hoeve JN, Schmitt MA. Ocular evaluation and genetic test for an early Alström Syndrome diagnosis. Am J Ophthalmol Case Rep. 2020 Aug 12;20:100873. doi: …