The human eye is a complex organ consisting of multiple compartments with unique and
specialized properties that reflect their varied functions. Although there have been …

X-linked Retinoschisis (XLRS) is an early-onset transretinal dystrophy, often with a
prominent macular component, that affects males and generally spares heterozygous …

Despite being the subject of intensive research, tuberculosis, caused by Mycobacterium
tuberculosis, remains at present the leading cause of death from an infectious agent …

Proteomic analysis is an attractive and powerful tool for characterizing the molecular profiles
of diseased tissues, such as the vitreous. The complexity of data available for analysis …

Purpose This scoping review summarizes the applications of artificial intelligence (AI) and
bioinformatics methodologies in analysis of ocular biofluid markers. The secondary objective …

Purpose: To investigate the molecular composition of subretinal fluid (SRF) in central serous
chorioretinopathy (CSCR) and rhegmatogenous retinal detachment (RRD) using proteomics …

Abstract Fragile X Syndrome (FXS), the most common inherited form of human intellectual
disability, is a monogenic neurodevelopmental disorder caused by a loss-of-function …

Introduction. Fibrinolysis is of key importance in maintaining vessel patency. Impaired
fibrinolysis associated with more compact fibrin structure has been shown in patients with …

X-linked retinoschisis (XLRS) is a retinal degenerative disorder caused by mutations in RS1
gene leading to splitting of retinal layers (schisis) which impairs visual signal processing …

X-linked retinoschisis (XLRS) is an inherited retinal degeneration affecting males,
characterized by splitting of the retinal layers. We herein present the outcomes of surgical …