Results 131 to 140 of about 15,974 (222)

Eight-year follow-up of phenotypic progression in a Chinese XLRP pedigree with a novel <i>RP2</i> gene mutation. [PDF]

Front Genet
Sun H, Shi J, Yang S, Tian H, Yang X, Xie G, Wei Y, Wang J.   +7 more
europepmc   +1 more source

Isolated Cone Dystrophy With Secondary Macular Involvement Mimicking Vascular Insult and Optic Atrophy: A Case Report. [PDF]

Cureus
Varghese DE, Sudhakar S.
europepmc   +1 more source

Longitudinal and cross-sectional study of retinal phenotypes and visual function in choroideremia carriers: a new grading system. [PDF]

Eye Vis (Lond)
Han X, Yu Y, Ding J, Sun Z, Li H, Zou X, Sui R.   +6 more
europepmc   +1 more source

Electroretinography biomarkers indicate disrupted visual processing in Fragile X syndrome. [PDF]

J Neurodev Disord
Pu Q, Bennett N, Sekhar TC, Stanley MT, Berry-Kravis E.   +4 more
europepmc   +1 more source

Electroretinography of Experimental Animals [PDF]

British Journal of Ophthalmology, 1950
openaire   +2 more sources

Persistent Bilateral Optic Disc Swelling in Non-Syndromic Retinitis Pigmentosa: A Case Report. [PDF]

Am J Case Rep
Alenazi M, Magliyah MS, Alsakran WA.
europepmc   +1 more source

Clinical Validation of a CRX Variant Leading to a Cone-Rod Dystrophy. [PDF]

Cureus
Pagán-Melvin C, Izquierdo N, Alejandro KC.   +2 more
europepmc   +1 more source

Focused Ultrasound Treatment of Vitreous Hemorrhage in an In Vivo Rabbit Model. [PDF]

Ophthalmol Sci
Yau GL, Ning B, Hu C, Hynynen K.
europepmc   +1 more source

Response to Comment on Uddin et al. Interpreting Retinal Hypoxia in Early Diabetes. [PDF]

Diabetes
Uddin MI.
europepmc   +1 more source

Genetic and Phenotypic Characterization of a Large Cohort of Patients with BBS1-Retinopathy. [PDF]

Ophthalmol Sci
Romo-Aguas JC, de Guimarāes TAC, Kalitzeos A, Alfaro-Goldaracena MDP, Baker RA, Robson AG, Fujinami K, Fujinami-Yokokawa Y, Mahroo OA, Webster AR, Michaelides M.   +10 more
europepmc   +1 more source