Results 91 to 100 of about 18,446 (279)
Prevalence of refractive error in Europe: the European Eye Epidemiology (E3) Consortium [PDF]
, 2015 To estimate the prevalence of refractive error in adults across Europe. Refractive data (mean spherical equivalent) collected between 1990 and 2013 from fifteen population-based cohort and cross-sectional studies of the European Eye Epidemiology (E3 ...
Anastasopoulos, E. (Eleftherios) +33 more
core +1 more source
The Natural Course of Bosch‐Boonstra‐Schaaf Optic Atrophy Syndrome
Clinical Genetics, EarlyView.Here, we present data on genetic variants and phenotype development of 47 individuals with Bosch‐Boonstra‐Schaaf optic atrophy syndrome, a rare neurodevelopmental disorder, highlighting the fact that the disease does not appear to be fundamentally progressive.
Ilia Valentin +4 more
wiley +1 more source
Monovision LASIK in emmetropic presbyopic patients. [PDF]
, 2018 BackgroundTo evaluate the efficacy and patient satisfaction of laser in situ keratomileusis (LASIK) monovision correction in presbyopic emmetropic patients.MethodsA retrospective review of 294 patients who underwent LASIK for monovision was conducted ...
Hannan, Stephen +4 more
core
Axial length growth and the risk of developing myopia in European children [PDF]
, 2018 PURPOSE: To generate percentile curves of axial length (AL) for European children, which can be used to estimate the risk of myopia in adulthood. METHODS: A total of 12 386 participants from the population-based studies Generation R (Dutch children ...
Boyd +51 more
core +3 more sources
A Novel UPF1 Variant Associated With a Rare UPF1‐Related Neurodevelopmental Disorder
Clinical Genetics, EarlyView.Nonsense‐mediated mRNA decay (NMD) plays a crucial role in degrading aberrant transcripts with premature termination codons, and aberrant NMD has been linked to neurodevelopmental disorders (NDD). A key player of NMD is UPF1, which is a helicase. Including the current patient, only four individuals with NDD and UPF1 variants have been reported in the ...
Zeynep Tümer +4 more
wiley +1 more source
Acta Medica Iranica, 2022 Aim: To report the five-year results of Trans-epithelial Photorefractive Keratectomy (TPRK) in treating all kinds of refractive errors. Methods: In this retrospective cohort study, we quantitatively compared the clinical findings and assessment of ...
Hamidreza Hasani +3 more
doaj
Prevalence and risk factors for myopia and other refractive errors in an adult population in southern India. [PDF]
, 2018 PURPOSE: To investigate prevalence and risk factors for myopia, hyperopia and astigmatism in southern India. METHODS: Randomly sampled villages were enumerated to identify people aged ≥40 years.
Bourne +37 more
core +1 more source
Aarskog Syndrome: Deep Phenotyping and Genomic Landscape of a New Cohort Including Adult Patients
Clinical Genetics, EarlyView.This study presents the deep phenotyping data of 14 new Aarskog‐Scott syndrome patients with molecular confirmation. ABSTRACT Aarskog‐Scott syndrome (AAS, MIM#305400) is an X‐linked disorder characterized by recognizable facial features, short stature, and genitourinary and skeletal malformations.
Gozde Tutku Turgut +7 more
wiley +1 more source
Phakic Intraocular Lenses An Overview
Delhi Journal of Ophthalmology, 2013 Currently, there are four general approaches to correct refractive errors: refractive corneal surgery, crystalline lens surgery, and implantation of an intraocular lens (IOL) in the anterior or posterior chamber.
Sana Ilyas Tinwala, J S Titiyal
doaj +1 more source
The effect of varying glucose levels on the ex vivo crystalline lens: implications for hyperglycaemia-induced refractive changes [PDF]
, 2014 Purpose: Refractive changes in diabetic eyes have long been reported but with equivocal results. The lens has been a more recent focus as the source of any change but it is possible that multiple sources of variation have made it difficult to demonstrate
Agardh +32 more
core +1 more source