Results 151 to 160 of about 6,473 (203)

Gene Therapy for Inherited Retinal Disease: Current Strategies, Personalized Medicine, and Future Implications-A Comprehensive Review. [PDF]

J Pers Med
Butt FR, Dhivagaran T, Li B, Ashamalla M, Tao BK, Balas M, Pereira A, Yan P, Arjmand P.   +8 more
europepmc   +1 more source

Application of 3D MRI and SS-OCT/OCTA in Assessment of Posterior Scleral Contraction for Myopic Traction Maculopathy. [PDF]

Transl Vis Sci Technol
Yu D, Wu D, Li H, Rong H, He Q, Zhang X, Xu H, Chai M, Zhou Y, Wei R.   +9 more
europepmc   +1 more source

Characteristics of Myopic Traction Maculopathy in the Aier-SERI High Myopia Adult Cohort Study. [PDF]

Ophthalmol Sci
Cheong KX, Jiang Y, Htoon HM, Pan W, Foo LL, Hu Z, Chen L, Ang S, Lamoureux EL, Hoang QV, Saw SM, Lan W.   +11 more
europepmc   +1 more source

Clinical features of early-onset high myopia in Chinese children: attention to comorbidities. [PDF]

BMC Ophthalmol
Ding Y, Xie F, Zhang J, Jiang M, Wang T, Wan X.   +5 more
europepmc   +1 more source

Quantitative evaluation of the wide-field fundus photographs in eyes with severe stage 3 and stage 4A retinopathy of prematurity. [PDF]

BMC Ophthalmol
Bayramoglu SE, Sayin N, Erdogan G.
europepmc   +1 more source

Angle closure glaucoma in a patient with X-linked retinoschisis: a case report. [PDF]

Int J Ophthalmol
Yao L, Lu Y, Yang KY, Lyu K, Wang ZY, Huang LZ, Wu HJ.   +6 more
europepmc   +1 more source

Handheld 400kHz optical coherence tomography angiography visualizes microvascular details in infants with advanced retinopathy of prematurity. [PDF]

Am J Ophthalmol Case Rep
Narawane A, Viehland C, Imperio R, Tran-Viet D, Mangalesh S, Izatt JA, Chen X, Toth CA.   +7 more
europepmc   +1 more source

Correction of Abnormal Head Position in Pediatric Nystagmus Using Yoked Low-Value Prism Glasses: A Retrospective Study. [PDF]

Invest Ophthalmol Vis Sci
Nsour G, Misawa MAM, Adamuccio J, Goldsmith M, Teplitski K, Markowitz S, Markowitz M, Markowitz SN, Daibert-Nido M.   +8 more
europepmc   +1 more source

A Case of FAM111A-Associated Kenny-Caffey Syndrome Type 2 with New Clinical Features: Microtia, Lacunar Skull Appearance, and Arnold-Chiari Malformation. [PDF]

Mol Syndromol
Doğan Arı AB, Türkyılmaz A, Keçeli AM, Önen M, Kılıç E.   +4 more
europepmc   +1 more source