Results 201 to 210 of about 233,851 (293)

Inflammation-induced lymphangiogenesis in the cornea arises from CD11b-positive macrophages.

open access: yesJournal of Clinical Investigation, 2005
K. Maruyama   +11 more
semanticscholar   +1 more source

Congenital aniridia: European COST action ANIRIDIA‐NET guidelines for diagnosis, management and care

open access: yesActa Ophthalmologica, EarlyView.
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

Expanding the Prenatal Phenotypic Spectrum of TRPV6 Variants With Ocular Anomalies

open access: yes
Prenatal Diagnosis, EarlyView.
Edouard Leyne   +7 more
wiley   +1 more source

The longitudinal associations of reading, writing and screen time with myopia at age 9 years among children from the GUSTO birth cohort

open access: yesActa Ophthalmologica, EarlyView.
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

P4HA2 Participates in Pathogenesis of Refractive Error by Regulating Collagen Posttranslational Modification and Extracellular Matrix Balance. [PDF]

open access: yesHum Mutat
Liu Y   +16 more
europepmc   +1 more source

Elastic modulus and collagen organization of the rabbit cornea: epithelium to endothelium.

open access: yesActa Biomaterialia, 2014
S. Thomasy   +7 more
semanticscholar   +1 more source

Exploring the histopathological signature of repeat‐mediated Fuchs endothelial corneal dystrophy

open access: yesActa Ophthalmologica, EarlyView.
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

Comparative Histology of the Cornea and Palisades of Vogt in Various Non-Human Primates. [PDF]

open access: yesVet Sci
Klećkowska-Nawrot J   +5 more
europepmc   +1 more source

Wounding the cornea to learn how it heals.

open access: yesExperimental Eye Research, 2014
M. Stepp   +6 more
semanticscholar   +1 more source

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