Results 241 to 250 of about 359,110 (364)
Abstract Purpose To assess the validity of the HelpMeSee Manual Small Incision Cataract Surgery (MSICS) module as a virtual reality training tool for technical skills and stress management in ophthalmology. Methods This prospective study enrolled 47 volunteer surgeons from five groups: four groups of eye surgeons with increasing experience (novice ...
Lea Dormegny +12 more
wiley +1 more source
Living histopathology - interrogation of ocular tissues by light: a celebration of the slit-lamp and a repertoire of clinical techniques. [PDF]
Meyer PAR.
europepmc +1 more source
An automatic diagnosis system of nuclear cataract using slit-lamp images
Haizhou Li +7 more
openalex +2 more sources
Abstract Purpose To investigate changes in choroidal and retinal thickness before and during myopia control treatment with orthokeratology lenses (OKL) in myopic children. Methods This was a sub‐study of CONTROL and CONTROL2 studies. The present study was a 2‐year, prospective, single‐group interventional study consisting of a 6‐month pre‐treatment ...
P. O. Hansen, F. Møller, T. M. Jakobsen
wiley +1 more source
Abstract Congenital aniridia is a rare genetic disorder primarily caused by pathogenic variants of the PAX6 gene. It leads to various panocular anomalies, including aniridia‐associated keratopathy (AAK). This review highlights recent insights into its pathogenesis, focusing on clinical staging, microstructural changes in the cornea and molecular ...
N. Szentmáry +27 more
wiley +1 more source
Abstract Kohl was ubiquitous in ancient Egypt and the Middle East, and routinely included among the toiletries deposited in burials. For Egypt, kohl recipes are increasingly well‐studied and known to use a range of inorganic and organic ingredients. Although these are often lead‐based, manganese‐ and silicon‐rich compounds are also attested.
Silvia Amicone +7 more
wiley +1 more source
A novel CPAMD8 nonsense mutation c.2679C>G (p.Tyr893*) was identified in a patient with congenital microcoria, leading to reduced mRNA expression and predicted protein truncation. ABSTRACT Congenital microcoria (MCOR) is a rare inherited ocular disorder. Here, we describe a novel nonsense variant in the CPAMD8 gene in a patient with MCOR.
Jing‐Fan Gao +4 more
wiley +1 more source
Diagnostic Assessment of Nuclear Cataracts Using a Smartphone-Attachable Slit-Lamp Device: A Cross-Sectional Study in Vietnam. [PDF]
Duong NM, Nguyen Vu NQ, Le HT.
europepmc +1 more source

