Results 161 to 170 of about 64,976 (308)
Genetic and molecular basis of congenital cataracts
Cataracts are caused when the lens of the eye (which focuses light), loses transparency. They typically occur in older individuals, but can also occur in children, even as early as from birth.
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Abstract Aim To evaluate the impact of initial mono‐ versus multitherapy on the ocular surface and related quality of life after 5 years follow‐up in the Glaucoma Intensive Treatment Study (GITS). Method The study included patients with primary open‐angle glaucoma and pseudoexfoliation glaucoma who completed 5‐year follow‐up in GITS.
Gauti Jóhannesson +6 more
wiley +1 more source
Candidate Genes for Non-Syndromic Pediatric Cataracts. [PDF]
Rossen JL +4 more
europepmc +1 more source
Abstract Purpose To evaluate the surgery‐induced changes of astigmatism after Descemet membrane endothelial keratoplasty (DMEK) in eyes with failed previous penetrating keratoplasty (PK). Design Retrospective, interventional cohort study based on prospective DMEK database.
Florian Thomas Steinberg +6 more
wiley +1 more source
Ocular Manifestations in Patients with Werner Syndrome. [PDF]
Oshitari T, Yamaga M, Maezawa Y.
europepmc +1 more source
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
<i>Myodes rufocanus</i> Cataract Identification and Transcriptome Analysis. [PDF]
Wang M +5 more
europepmc +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
Hyperhomocysteinemia as a Common Denominator: Linking Posterior Subcapsular Cataract and Pulmonary Thromboembolism. [PDF]
Jain A, Luthra V, Gupta R, Kaushik A.
europepmc +1 more source

