Decellularized corneal-based 3D scaffolds: methods decellularization, characterization, mechanical properties, and species source. [PDF]
Akbaripour V +5 more
europepmc +1 more source
Threat to fixation and vision‐related quality of life in patients with open‐angle glaucoma
Abstract Purpose We aimed to investigate the association between overlapping threat to fixation (TTF) and vision‐related quality of life (VRQoL) in patients with manifest open‐angle glaucoma (OAG). Methods Overall, 316 patients with manifest OAG were recruited from the glaucoma outpatient department of Skåne University Hospital, Malmö, Sweden, between ...
Charlotte Almer, Dorothea Peters
wiley +1 more source
Alterations in Mitochondrial DNA in Corneal Fibroblast and Myofibroblast Post Injury. [PDF]
Sinha NR +5 more
europepmc +1 more source
Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care
Abstract Congenital aniridia is a rare ocular disorder affecting the majority of eye structures and can be associated with systemic manifestations. The main visible phenotypic characteristic is the partial or complete absence of the iris; however, foveal hypoplasia is a more frequent and reliable clinical sign. Other ocular comorbidities are associated
Davide Romano +26 more
wiley +1 more source
A pilot study for decellularizing porcine cornea for future use in corneal regeneration. [PDF]
Josifovska N +5 more
europepmc +1 more source
Abstract Purpose To investigate the associations between paper‐based reading and writing time, screen‐based time at ages 2, 3, 6 and 9 years and myopia at age 9 in the GUSTO birth cohort. Methods The GUSTO study recruited pregnant women from two Singapore public maternity hospitals between 2009 and 2010. Parent‐reported reading and writing time, screen
Fan Wu +7 more
wiley +1 more source
Cataract surgery with autosomal recessive cornea plana caused by a novel <i>KERA</i> mutation. [PDF]
Abdalla Elsayed MEA, MacLaren RE.
europepmc +1 more source
Exploring the histopathological signature of repeat‐mediated Fuchs endothelial corneal dystrophy
Abstract Purpose To determine the histological differences between Fuchs endothelial corneal dystrophy (FECD) cases with and without the most common genetic risk factor, expansion of a CTG repeat (CTG18.1) within the TCF4 gene. Methods Formalin‐fixed paraffin‐embedded corneal tissues were compared retrospectively, and CTG18.1 status was determined from
Anne‐Marie S. Kladny +5 more
wiley +1 more source
Preferred practice patterns in the management of keratoconus: a national survey of cornea specialists in Saudi Arabia. [PDF]
AlJohani S +3 more
europepmc +1 more source

