Results 161 to 170 of about 22,493 (269)
Aqueous humour concentrations of HB‐EGF, EGF and VEGF‐A and axial length in humans
Abstract Purpose To investigate relationships between the intraocular concentrations of heparin‐binding epidermal growth factor (HB‐EGF), epidermal growth factor (EGF) and vascular endothelial growth factor A (VEGF‐A) in dependence on axial length in humans. Design Clinical interventional cohort study.
Wen‐Da Zhou +8 more
wiley +1 more source
Changes in the Ocular Biometric Measurements of Korean Children with Myopia and Hyperopia [PDF]
Ji Eon Kang +2 more
openalex +1 more source
This study reports six new cases of 22q13.2 duplication and triplication, including the TCF20 gene, associated with neurodevelopmental disorders and various morphological and systemic abnormalities. The findings suggest a variable expressivity, but their complete penetrance remains uncertain compared to well‐established loss‐of‐function variants ...
Etienne Bizot +13 more
wiley +1 more source
An Analysis of Some Refractive Error Trends in US Air Force Pilots and Navigators [PDF]
Refractive error trends with age in US Air Force pilots and ...
Dunsky, I. L., Levene, J. R.
core +1 more source
‘Green Skills’ : What Do Companies Do With It? The Case of Building Automation
ABSTRACT In recent times, ‘Green Skills’ has become a buzzword in international, national and local policies. Green Skills are considered to be an important precondition to achieving the United Nations' Sustainable Development Goals. However, until now, there has been a research gap in how companies, characterised by the particularities of their ...
Martina Fuchs +3 more
wiley +1 more source
Hyperopia is a type of refractive error and photorefractive keratectomy (PRK) is one of the surgical procedures for correction of various types of refractive errors.
Hassan Razmjoo +4 more
doaj
AP2M1 Is a Candidate Gene for Microcephaly and Intellectual Disability in 3q27.1 Deletions
ABSTRACT Deletions of the 3q26.33q27.2 region appear to correlate with a distinct phenotype, although there are few reported cases. Here, we present seven previously unreported individuals carrying de novo 3q27 deletions (under 5 Mb), which include the AP2M1 (adaptor‐related protein complex 2, mu‐1 subunit) gene and summarize data from 12 previously ...
Russell Gear +16 more
wiley +1 more source
Transepithelial Photorefractive Keratectomy for Hyperopia Correction: An Uncharted Territory
Swapnali Sabhapandit +3 more
openalex +2 more sources
Evaluation of 80 Mexican patients with suspected 22q11.2 deletion syndrome, including detailed phenotypic characterization. Multiplex ligation‐dependent probe amplification identified both typical and atypical deletions, underscoring the need for complementary approaches to fluorescence in situ hybridization.
Thania Alejandra Aguayo‐Orozco +7 more
wiley +1 more source

