Background: Acute macular neuroretinopathy (AMN) is an increasingly diagnosed disorder
associated with several diseases. The aim of this study was to report the incidence of AMN …

Purpose: To investigate the impact of reticular pseudodrusen on macular function using
microperimetry. Methods: Eighteen consecutive patients (18 eyes) with reticular pseudodrusen (…

Optogenetics may enable mutation-independent, circuit-specific restoration of neuronal
function in neurological diseases. Retinitis pigmentosa is a neurodegenerative eye disease …

Background: Canadian health funding currently prioritizes scaling up for evidence-based
primary care innovations, but not all teams prepare for scaling up. We explored scalability …

Background Cone and cone-rod dystrophies are clinically and genetically heterogeneous
inherited retinal disorders with predominant cone impairment. They should be distinguished …

Besides cystoid macular edema due to a blood-retinal barrier breakdown, another type of
macular cystoid spaces referred to as non-vasogenic cystoid maculopathies (NVCM) may be …

MER tyrosine kinase (MERTK) encodes a surface receptor localized at the apical membrane
of the retinal pigment epithelium. It plays a critical role in photoreceptor outer segment …

Background To evaluate the anatomical and functional outcomes of intravitreal dexamethasone
implant in patients with macular edema (ME) secondary to retinitis pigmentosa (RP). …

The natural history of CVJ stenosis in achondroplastic children is only partially known.
Achondroplastic children have a foramen magnum that is significatively smaller at birth, and it …

Variants of the TTLL5 gene, which encodes tubulin tyrosine ligase-like family member five,
are a rare cause of cone dystrophy (COD) or cone-rod dystrophy (CORD). To date, only a few …