Ji S. Min
Seoul, Republic of Korea
Last Updated: 09/26/2026
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Found 18 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
Changes in corneal symmetry and tear film stability after laser asymmetric keratectomy in patients with keratoconus suspect: A retrospective study.
Journal: Medicine
Published: April 15, 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
A Novel Corneal Remodeling Technique of Laser Asymmetric Keratectomy in Keratoconus Suspect: A Retrospective Case Control Study.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: August 16, 2024
The Effect of Alternating Monocular Instillation of 0.125% Atropine in Korean Children with Progressive Myopia.
Journal: Journal of clinical medicine
Published: July 10, 2024
Comparison of Intense Pulsed Light Treatments including Upper Lid or Lateral Canthus in Patients of Meibomian Gland Dysfunction.
Journal: Journal of clinical medicine
Published: May 13, 2024
Anterior segment characteristics in normal and keratoconus eyes evaluated with a new type of swept-source optical coherence tomography.
Journal: PloS one
Published: March 30, 2022
Skin temperature change in patients with meibomian gland dysfunction following intense pulsed light treatment.
Journal: Frontiers in medicine
Published: March 11, 2022
A Novel Approach to Enhancement Linked Laser Asymmetric Keratectomy Using Semi-Cylindrical Ablation Pattern in Patients with Myopic Regression After Laser Refractive Surgery.
Journal: Clinical ophthalmology (Auckland, N.Z.)
Published: February 14, 2021
Compound heterozygous mutations in TGFBI cause a severe phenotype of granular corneal dystrophy type 2.
Journal: Scientific reports
Published: January 30, 2021
Last Updated: 09/26/2026