Last Updated: 09/26/2026
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Found 48 publications
A case of paternity-confirmed de novo R124H mutation resulting in granular corneal dystrophy type 2.
A case of paternity-confirmed de novo R124H mutation resulting in granular corneal dystrophy type 2.
Journal: Ophthalmic genetics
Published: June 25, 2025
Slow granular corneal dystrophy type 2 exacerbation after SMILE: a bilateral asymmetric case resembling a unique previous unilateral case.
Journal: International journal of ophthalmology
Published: June 10, 2025
Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in TGFBI: Phenotype, Genotype, and Treatment.
Journal: Genes
Published: November 13, 2024
Standards for analyzing astigmatic outcomes: Part I: astigmatism basics.
Journal: Journal of cataract and refractive surgery
Published: October 20, 2024
Standards for analyzing astigmatic outcomes: Part II: Recommended statistical methods.
Journal: Journal of cataract and refractive surgery
Published: October 20, 2024
Long Term Corneal Flattening After Corneal Crosslinking in Patients with Progressive Keratoconus.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: April 03, 2023
Reply : Clinical and refractive outcomes after topography-guided refractive surgery planned using Phorcides surgery planning software.
Journal: Journal of cataract and refractive surgery
Published: November 03, 2022
De Novo L509P Mutation of the TGFBI Gene Associated with Slit-Lamp Findings of Lattice Corneal Dystrophy Type IIIA.
Journal: Journal of clinical medicine
Published: April 22, 2022
A Randomized Trial of Topical Fibrinogen-Depleted Human Platelet Lysate Treatment of Dry Eye Secondary to Chronic Graft-versus-Host Disease.
Journal: Ophthalmology science
Published: January 10, 2022
Clinical and refractive outcomes after topography-guided refractive surgery planned using Phorcides surgery planning software.
Journal: Journal of cataract and refractive surgery
Published: October 03, 2021
Last Updated: 09/26/2026