Results 151 to 160 of about 615,247 (279)
Clinical manifestations of dual‐gene variants in retinitis pigmentosa
Acta Ophthalmologica, EarlyView.Abstract Purpose Retinitis pigmentosa (RP) is an inherited retinal disease (IRD), whereby each affected individual typically harbours pathogenic variants in a single causative gene, yet the disorder exhibits marked genetic heterogeneity, with more than 100 genes reported to underlie RP.
Lasse Wolfram +11 more
wiley +1 more source
Henle Fibers Are Organized in Bundles Consistent Between Individuals and Conserved in Primates. [PDF]
Invest Ophthalmol Vis SciWong-Fortunato J +8 more
europepmc +1 more source
Macular Star and Choroidal Tubercles: A Rare Cause of Opticospinal Syndrome [PDF]
Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques, 2019 Arunmozhimaran Elavarasi +2 more
openaire +1 more source
Retinal dystrophies simulating geographic atrophy: A diagnostic challenge
Acta Ophthalmologica, EarlyView.Abstract Geographic atrophy (GA) is the chronic loss of retinal pigment epithelium, photoreceptors and choriocapillaris, marking the dry late stage of age‐related macular degeneration (AMD). GA prevalence is expected to rise in the upcoming decades. Advanced GA leads to central scotomas, reducing visual acuity and quality of life, potentially resulting
Johanna M. Colijn +3 more
wiley +1 more source
Acta Ophthalmologica, EarlyView.Abstract Purpose Proliferative diabetic retinopathy (PDR) is one of the leading causes of blindness in working‐age adults. We have previously shown that the risk of PDR is significantly elevated in individuals with intrauterine exposure to famine. However, the genetic mechanisms mediating this association remain unknown.
Olena Fedotkina +7 more
wiley +1 more source
Neuroretinitis Secondary to Toxoplasma Infection in an Adult. [PDF]
Case Rep Ophthalmol MedLadak S, Siddiqui MAR.
europepmc +1 more source