Results 71 to 80 of about 30,062 (169)
ABSTRACT Background Refractive errors are the leading cause of preventable visual impairment worldwide, yet data from isolated Indigenous populations remain virtually absent from the global literature. The Yanomami, one of the largest Indigenous peoples in the Americas with recent and limited contact with non‐Indigenous society, have no prior ...
Maria Christina Chagas Ferreira +2 more
wiley +1 more source
Reduced order modelling of air‐puff test for corneal material characterisation
Abstract Models of the fluid–structure interaction (FSI) model for the air‐puff test were analysed. Using Abaqus, the air‐puff test is applied to eyes with varying biomechanical parameters, such as material properties, corneal thickness, and radius.
Osama M. Maklad, Muting Hao
wiley +1 more source
Quantitative evaluation of LED‐based optical autofocus module
Abstract We report an improved version of the open‐source optical autofocus (OAF) module (openAF) for light microscopy, replacing the superluminescent diode (SLD) with a multimode‐optical fibre‐coupled LED as a more accessible AF module light source. We also present a method for independently quantifying AF system performance using 2D autocorrelation ...
S. Habte +5 more
wiley +1 more source
Abstract Modulation of bone marrow adipose tissue (BMAT) with prolonged inactivity was reported in haemopoietic but not in non‐haemopoietic bones. This prospective randomized controlled trial submitted 16 men and 8 women to 60 days of 6° head‐down‐tilt bed rest.
Tammy Liu +5 more
wiley +1 more source
ABSTRACT Rationale Quantum cascade laser absorption spectroscopy (QCLAS) is a fast and reliable method for analyzing the bulk (𝛿13C‐CH4, 𝛿D‐CH4) and clumped isotopic (∆13CH3D and ∆12CH2D2) composition of methane. However, precise measurements of ∆12CH2D2 require 0.5 to 1.8 mmol of purified methane (equivalent to 15 to 40 mL at STP).
Nico Kueter +6 more
wiley +1 more source
Manoj Motwani, Lourdes Haydaw Cornea Revolution/Motwani, LASIK Institute, San Diego, CA, 92121, USACorrespondence: Manoj Motwani, Cornea Revolution/Motwani, LASIK Institute, 9710 Scranton Road, Ste 170, San Diego, CA, 92121, USA, Tel +1 858 554-0008 ...
Motwani M, Haydaw L
doaj
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli +18 more
wiley +1 more source
We describe a previously unreported phenotype related to postzygotic ACTB variants with hypomelanosis of Ito, characterized by hypopigmentation associated or not with neurodevelopmental features, distinct from Becker presentations, bridging constitutional neurodevelopmental and somatic cutaneous phenotypes.
Estella Castillon +9 more
wiley +1 more source
Objectives To investigate the impact of residual refraction within ±1.0 dioptre (D) on uncorrected distance visual acuity (UDVA) in pseudophakic eyes.Design Cross-sectional study.Setting This study was based on retrospectively collected electronic ...
Ling Jin +7 more
doaj +1 more source
USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes
Heterozygous loss‐of‐function variants in USP34 cause a novel neurodevelopmental disorder characterized by global developmental delay, speech impairment, autism, hypotonia, craniofacial dysmorphism, and distal limb anomalies. Disrupted Wnt/β‐catenin signaling via reduced Axin stabilization refines gene‐specific contributions within 2p15p16.1 ...
Helena Wigoda +10 more
wiley +1 more source

