Results 31 to 40 of about 152,878 (215)

Corneal cross‐linking as a treatment for corneal dystrophy with secondary bacterial infection in a Friesian horse [PDF]

open access: yes, 2020
Corneal cross-linking should be considered as treatment option in Friesian horses with infectious keratitis and corneal dystrophy.
Pot, Simon A; https://orcid.org/   +11 more
core   +1 more source

The IC3D Classification of the Corneal Dystrophies [PDF]

open access: yesCornea, 2008
The recent availability of genetic analyses has demonstrated the shortcomings of the current phenotypic method of corneal dystrophy classification. Abnormalities in different genes can cause a single phenotype, whereas different defects in a single gene can cause different phenotypes.
Weiss, JS   +16 more
openaire   +3 more sources

Expression and Function of ZEB1 in the Cornea

open access: yesCells, 2021
ZEB1 is an important transcription factor for epithelial to mesenchymal transition (EMT) and in the regulation of cell differentiation and transformation.
Yingnan Zhang   +5 more
doaj   +1 more source

Molecular Pathogenesis of Corneal Dystrophies: Schnyder Dystrophy and Granular Corneal Dystrophy type 2

open access: yes, 2015
The International Committee for Classification of Corneal Dystrophies (IC3D) provides updated data to ophthalmologists by incorporating traditional definitions of corneal dystrophies with new genetic, clinical, and pathologic information. Recent advances
최승일, 이훈, 김응권
core   +1 more source

Fuchs’ endothelial corneal dystrophy RNA sequencing datasets for meta-analysis.

open access: yes, 2023
Fuchs’ endothelial corneal dystrophy RNA sequencing datasets for meta-analysis.
V. Vinod Mootha (6264278)   +4 more
core   +1 more source

Modern aspects of therapy of primary and secondary dystrophies of the cornea

open access: yesРоссийский офтальмологический журнал, 2018
Dystrophy of the cornea is a pathological condition characterized by various manifestations of chronic corneal nutrition disorders. Surgical treatment of corneal dystrophy remains insufficiently available in many regions of Russia.
E. S. Vakhova   +2 more
doaj   +1 more source

Corneal Fleck dystrophy in a Spanish family

open access: yes, 2020
Corneal fleck dystrophy is an unusual, asymptomatic, autosomal dominant condition. In the pathogenesis, it is hypothesized that a hydrolytic enzyme deficiency of keratocytes is involved, leading to accumulation of mucopolysaccharides and intracellular ...
Rodríguez Calvo de Mora, Marina   +7 more
core   +1 more source

Navigating the Complexity: A Comprehensive Review of GSK‐3 Inhibition in Regenerative Medicine

open access: yesMedicinal Research Reviews, EarlyView.
ABSTRACT Glycogen synthase kinase‐3 (GSK‐3) is a central regulator of numerous cellular signaling pathways, with critical roles in metabolism, proliferation, differentiation, and tissue regeneration. This review explores the multifaceted effects of pharmacological GSK‐3 inhibition across multiple body districts, focusing on its highly context‐dependent
Davide Schiroli   +5 more
wiley   +1 more source

Optimal Resources for Children's Surgery 2: Tiered Recommendations for Minimum Essential Children's Surgical Procedures Across Health System Levels

open access: yesWorld Journal of Surgery, EarlyView.
In 2015 the World Health Assembly (WHO), based on recommendations by the Lancet Commission on Global Surgery, passed resolution (68:15) on strengthening emergency and essential surgical care and anesthesia as a component of universal health coverage. However, children's surgery was not adequately represented and in response, the Global Initiative for ...
Arpita Biswangree   +121 more
wiley   +1 more source

Detailed corneal and genetic characteristics of a pediatric patient with macular corneal dystrophy - case report

open access: yesBMC Ophthalmology, 2021
Background Corneal dystrophies are a group of rare, inherited disorders that are usually bilateral, symmetric, slowly progressive, and not related to environmental or systemic factors. The majority of publications present the advanced form of the disease
Anna Nowińska   +5 more
doaj   +1 more source

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