Sep 3, 2026 | Government, News, Science
Am J Ophthalmol. 2026 Sep 3:S0002-9394(26)00501-5. doi: 10.1016/j.ajo.2026.08.044. Online ahead of print.ABSTRACTPURPOSE: To describe the molecular genetic spectrum and age-related clinical features of USH2A-associated retinitis pigmentosa in Korean patients.DESIGN:...
Sep 3, 2026 | Government, News, Science
JAMA Ophthalmol. 2026 Sep 3. doi: 10.1001/jamaophthalmol.2026.3926. Online ahead of print.NO ABSTRACTPMID:42690644 | DOI:10.1001/jamaophthalmol.2026.3926
Sep 3, 2026 | Government, News, Science
JAMA Ophthalmol. 2026 Sep 3:e263662. doi: 10.1001/jamaophthalmol.2026.3662. Online ahead of print.ABSTRACTIMPORTANCE: Stargardt disease (STGD) is the most common macular dystrophy, resulting in profound loss of vision. There is no approved treatment.OBJECTIVE: To...
Sep 2, 2026 | Government, News, Science
Biol Pharm Bull. 2026;49(9):1371-1375. doi: 10.1248/bpb.b26-00363.ABSTRACTRetinitis pigmentosa (RP) is an inherited retinal disorder characterized by the progressive degeneration of photoreceptor cells, representing a leading cause of blindness. A substantial...
Aug 31, 2026 | Government, News, Science
N Engl J Med. 2026 Aug 29. doi: 10.1056/NEJMoa2608903. Online ahead of print.ABSTRACTBACKGROUND: Many patients with suspected acute coronary syndrome in whom myocardial infarction has been ruled out in the emergency department remain at risk for cardiovascular events....
Aug 29, 2026 | Government, News, Science
Cell Rep. 2026 Aug 28;45(9):117906. doi: 10.1016/j.celrep.2026.117906. Online ahead of print.ABSTRACTCiliopathies comprise a spectrum of disorders involving mutations in over 150 genes affecting the primary cilium, with retinal degeneration as a prominent feature...
