Allon G, Lin S, Robson A, Arno G, Neveu M, Hysi P
Invest Ophthalmol Vis Sci. 2025; 66(2):50.
PMID: 39969478
PMC: 11841689.
DOI: 10.1167/iovs.66.2.50.
Yu M, Vieta-Ferrer E, Bakdalieh A, Tsai T
Int J Mol Sci. 2025; 26(3).
PMID: 39940729
PMC: 11816691.
DOI: 10.3390/ijms26030957.
Yeo E, Kominami T, Tan T, Babu L, Ong K, Tan W
Transl Vis Sci Technol. 2025; 14(2):16.
PMID: 39932467
PMC: 11817848.
DOI: 10.1167/tvst.14.2.16.
Man T, Yip Y, Pang C, Brelen M
Sci Rep. 2025; 15(1):4887.
PMID: 39929888
PMC: 11811280.
DOI: 10.1038/s41598-025-86750-0.
Brodie S, Faruque P, Pincay J, Sylla M, Cui X, Choi S
Doc Ophthalmol. 2025; .
PMID: 39903329
DOI: 10.1007/s10633-025-10003-8.
Comparisons of oscillatory potentials and 30 Hz flicker electroretinograms for discriminating eyes with diabetic retinopathy from normal eyes.
Gonmori M, Machida S, Inoue S, Ebihara S, Misu K
Jpn J Ophthalmol. 2025; 69(1):49-58.
PMID: 39883242
DOI: 10.1007/s10384-024-01154-3.
Hilbert transform analysis of the mouse scotopic electroretinogram reveals two distinct bursts of oscillatory potentials with progressively dimmer flashes.
Gauthier M, Polosa A, Lina J, Lachapelle P
Doc Ophthalmol. 2025; 150(1):1-15.
PMID: 39875716
DOI: 10.1007/s10633-025-10002-9.
Advancing Insights into Pediatric Macular Diseases: A Comprehensive Review.
Ambrosio L, Perepelkina T, Elhusseiny A, Fulton A, Gonzalez Monroy J
J Clin Med. 2025; 14(2).
PMID: 39860622
PMC: 11765775.
DOI: 10.3390/jcm14020614.
Atypical Leber Hereditary Optic Neuropathy (LHON) Associated with a Novel MT-CYB:m.15309T>C(Ile188Thr) Variant.
Petrovic Pajic S, Fakin A, Jarc-Vidmar M, Sustar Habjan M, Malinar L, Pavlovic K
Genes (Basel). 2025; 16(1).
PMID: 39858655
PMC: 11764998.
DOI: 10.3390/genes16010108.
Effects of Selected Antioxidants on Electroretinography in Rodent Diabetic Retinopathy.
Dutczak R, Pietrucha-Dutczak M
Antioxidants (Basel). 2025; 14(1).
PMID: 39857355
PMC: 11762402.
DOI: 10.3390/antiox14010021.
Spectral Analysis of Light-Adapted Electroretinograms in Neurodevelopmental Disorders: Classification with Machine Learning.
Constable P, Pinzon-Arenas J, Mercado Diaz L, Lee I, Marmolejo-Ramos F, Loh L
Bioengineering (Basel). 2025; 12(1).
PMID: 39851292
PMC: 11761560.
DOI: 10.3390/bioengineering12010015.
Remodeling the light-adapted electroretinogram using a bayesian statistical approach.
Brabec M, Marmolejo-Ramos F, Loh L, Lee I, Kulyabin M, Zhdanov A
BMC Res Notes. 2025; 18(1):33.
PMID: 39849598
PMC: 11760095.
DOI: 10.1186/s13104-025-07115-4.
De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa.
Quinodoz M, Rodenburg K, Cvackova Z, Kaminska K, de Bruijn S, Iglesias-Romero A
medRxiv. 2025; .
PMID: 39830270
PMC: 11741465.
DOI: 10.1101/2025.01.06.24317169.
Longitudinal assessment of retinal and visual pathway electrophysiology and structure after high altitude exposure.
Shi X, Li M, Zhang X, Yuan F, Liu Y, Lin J
Graefes Arch Clin Exp Ophthalmol. 2025; .
PMID: 39820514
DOI: 10.1007/s00417-024-06729-x.
Age- and Sex-Specific Regulation of Serine Racemase in the Retina of an Alzheimer's Disease Mouse.
Wang Y, Xu D, Zhao Y, Zhu H, Xiu X, Jiang H
Invest Ophthalmol Vis Sci. 2025; 66(1):36.
PMID: 39813057
PMC: 11741067.
DOI: 10.1167/iovs.66.1.36.
Longitudinal Assessment of Structural and Functional Changes in Rod-cone Dystrophy: A 10-year Follow-up Study.
Britten-Jones A, Luu C, Jolly J, Abbott C, Allen P, Lamey T
Ophthalmol Sci. 2025; 5(2):100649.
PMID: 39811267
PMC: 11731193.
DOI: 10.1016/j.xops.2024.100649.
Broadband Long Wavelength Light Promotes Myopic Eye Growth and Alters Retinal Responses to Light Offset in Chick.
Riddell N, Murphy M, Zahra S, Robertson-Dixon I, Crewther S
Invest Ophthalmol Vis Sci. 2025; 66(1):30.
PMID: 39804628
PMC: 11734760.
DOI: 10.1167/iovs.66.1.30.
Retinal Dystrophy Associated with Homozygous Variants in .
Maggi J, Hanson J, Kurmann L, Koller S, Feil S, Gerth-Kahlert C
Genes (Basel). 2025; 15(12.
PMID: 39766861
PMC: 11675615.
DOI: 10.3390/genes15121594.
Association analyses of the measurements of the photopic negative response evoked by two ISCEV protocols.
Zhang B, Wang J, Wang Y, Jiang Y, Zhao Y
Graefes Arch Clin Exp Ophthalmol. 2024; .
PMID: 39710709
DOI: 10.1007/s00417-024-06718-0.
A homozygous structural variant of is frequently associated with achromatopsia in Japanese patients with IRD.
Suga A, Mizobuchi K, Inooka T, Yoshitake K, Minematsu N, Tsunoda K
Genet Med Open. 2024; 2:101843.
PMID: 39669618
PMC: 11613597.
DOI: 10.1016/j.gimo.2024.101843.