Evangelia S. Panagiotou
Thessaloniki, ESYE12, Greece
Last Updated: 09/26/2026
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Found 11 publications
Functionally deficient UBOX5 variants and primary angle-closure glaucoma.
Journal: Nature communications
Published: July 31, 2024
Variants in the AGBL5 gene are responsible for autosomal recessive Retinitis pigmentosa with hearing loss.
Journal: European journal of human genetics : EJHG
Published: May 02, 2024
A New Technique with Scleral Grooves for Sutureless Scleral Fixation of the Carlevale Intraocular Lens.
Journal: Ophthalmology and therapy
Published: April 18, 2024
Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
Journal: Molecular vision
Published: December 18, 2021
Management of Full-Thickness Macular Hole in A Genetically Confirmed Case with Usher Syndrome.
Journal: Ophthalmology and therapy
Published: May 12, 2020
How Successful is Switching from Bevacizumab or Ranibizumab to Aflibercept in Age-Related Macular Degeneration? A Systematic Overview.
Journal: Advances in therapy
Published: January 08, 2019
Preservative-free tafluprost/timolol fixed combination: comparative 24-h efficacy administered morning or evening in open-angle glaucoma patients.
Journal: Expert opinion on pharmacotherapy
Published: October 18, 2018
Defects in the Cell Signaling Mediator β-Catenin Cause the Retinal Vascular Condition FEVR.
Journal: American journal of human genetics
Published: April 19, 2017
Twenty-four-hour intraocular pressure monitoring in normotensive patients undergoing chronic hemodialysis.
Journal: European journal of ophthalmology
Published: June 15, 2015
Novel C8orf37 mutations cause retinitis pigmentosa in consanguineous families of Pakistani origin.
Journal: Molecular vision
Published: September 22, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026