Characterisation and prevalence of inherited retinal diseases in the Finnish population reveals enrichment of population-specific phenotypes and causative variants. [PDF]
Br J OphthalmolLähteenoja L +3 more
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Star of the Diabetic Macular Show: Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis (SNIFR). [PDF]
J Ophthalmic Vis ResChristensen CA, Gupta N, Breazzano MP.
europepmc +1 more source
Acute retinal necrosis during the systemic use of Janus kinase inhibitor. [PDF]
Int J Retina VitreousWatanabe D +12 more
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Dark Rearing Does Not Alter Developmental Retinoschisis Cavity Formation in Rs1 Gene Knockout Rat Model of X-Linked Retinoschisis. [PDF]
Genes (Basel)Smit-McBride Z +4 more
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Progress of iPSC-derived retinal organoids in the study of inherited retinal diseases. [PDF]
Orphanet J Rare DisLiu B, Liu Y, Zhang H, Huang J, Liu G.
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Application of ultra-wide-field optical coherence tomography angiography in detecting peripheral lattice degeneration. [PDF]
Int OphthalmolCai C +7 more
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PROGRESSIVE MACULOPATHY IN A CHILD RESULTING FROM VITREOPAPILLARY TRACTION ON A CONGENITALLY ANOMALOUS NERVE. [PDF]
Retin Cases Brief RepKennamer-Chapman RM +2 more
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A Rare Vitreoretinal Degenerative Disorder: Goldmann-Favre Syndrome Complicated with Choroidal Neovascularization in a Pediatric Patient. [PDF]
Diagnostics (Basel)Szala K, Wójcik-Niklewska B.
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Spontaneous Resolution and Asynchronous Onset of Stellate Nonhereditary Idiopathic Foveomacular Retinoschisis in the Contralateral Eye. [PDF]
J Vitreoretin DisBayram-Suverza M, Ramírez-Estudillo A.
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