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Korean Journal of Ophthalmology : KJO
|
March 23, 2023
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee
Jinu Han, Kwangsic Joo, Ungsoo Samuel Kim, et al.
Genes
|
January 25, 2025
Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in <i>TGFBI</i>: Phenotype, Genotype, and Treatment
Ji Sang Min, Tae-Im Kim, Ikhyun Jun, et al.
Frontiers in Neurology
|
September 8, 2022
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy
Yuri Seo, Tae Young Kim, Dongju Won, et al.
Journal of Ophthalmology
|
September 19, 2022
Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study
Kyung-Ah Park, Hee Kyung Yang, Jinu Han, et al.
Genes
|
May 27, 2023
Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans
Dong Geun Kim, Kwangsic Joo, Jinu Han, et al.
Scientific Reports
|
June 29, 2021
In Silico identification of a common mobile element insertion in exon 4 of RP1
Dongju Won, Joo-Yeon Hwang, Yeeun Shim, et al.
Translational Vision Science & Technology
|
February 18, 2026
A Dosage-Dependent Dominant-Negative Mechanism of SLC45A2(W74R) in Autosomal Dominant Oculocutaneous Albinism Revealed by Zebrafish Modeling
Dongheon Surl, Tae-Ik Choi, Ji-Won Park, et al.
Genes
|
October 23, 2021
Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1
Soon-Il Choi, Se-Joon Woo, Baek-Lok Oh, et al.
NPJ Genomic Medicine
|
April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity
Riccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
October 18, 2023
Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea
Yeji Moon, Kyung-Ah Park, Jinu Han, et al.
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Search research articles
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Showing results (81-90 of 102) with videos related to
Sort By:
Page
of 11
Korean Journal of Ophthalmology : KJO
|
March 23, 2023
Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee
Jinu Han, Kwangsic Joo, Ungsoo Samuel Kim, et al.
Genes
|
January 25, 2025
Compound Heterozygous p.(R124C) (Classic Lattice Corneal Dystrophy) and p.(R124H) (Granular Corneal Dystrophy Type 2) in <i>TGFBI</i>: Phenotype, Genotype, and Treatment
Ji Sang Min, Tae-Im Kim, Ikhyun Jun, et al.
Frontiers in Neurology
|
September 8, 2022
Genetic spectrum and characteristics of autosomal optic neuropathy in Korean: Use of next-generation sequencing in suspected hereditary optic atrophy
Yuri Seo, Tae Young Kim, Dongju Won, et al.
Journal of Ophthalmology
|
September 19, 2022
Characteristics of Optic Neuritis in South Korean Children and Adolescents: A Retrospective Multicenter Study
Kyung-Ah Park, Hee Kyung Yang, Jinu Han, et al.
Genes
|
May 27, 2023
Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans
Dong Geun Kim, Kwangsic Joo, Jinu Han, et al.
Scientific Reports
|
June 29, 2021
In Silico identification of a common mobile element insertion in exon 4 of RP1
Dongju Won, Joo-Yeon Hwang, Yeeun Shim, et al.
Translational Vision Science & Technology
|
February 18, 2026
A Dosage-Dependent Dominant-Negative Mechanism of SLC45A2(W74R) in Autosomal Dominant Oculocutaneous Albinism Revealed by Zebrafish Modeling
Dongheon Surl, Tae-Ik Choi, Ji-Won Park, et al.
Genes
|
October 23, 2021
Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1
Soon-Il Choi, Se-Joon Woo, Baek-Lok Oh, et al.
NPJ Genomic Medicine
|
April 10, 2026
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic and syndromic retinal degeneration of variable severity
Riccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
October 18, 2023
Risk of central nervous system demyelinating attack or optic neuritis recurrence after pediatric optic neuritis in Korea
Yeji Moon, Kyung-Ah Park, Jinu Han, et al.
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of 11