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Korean Journal of Ophthalmology : KJO
|
June 30, 2025
Therapeutic Effect of Topical 0.125% Atropine in South Korean Myopic Children: A Real-World Experience
Dae Hee Kim, Jinu Han, Kyung-Ah Park, et al.
Scientific Reports
|
October 14, 2024
Proteomic analysis of CD29+ Müller cells reveals metabolic reprogramming in rabbit myopia model
Chae-Eun Moon, Jun-Ki Lee, Hyunjin Kim, et al.
Epidemiologia (Basel, Switzerland)
|
November 24, 2025
Clinical Features According to the Type of Intermittent Exotropia: Korean Intermittent Exotropia Multicenter Study
Hee Kyung Yang, Hae Ri Yum, Sun A Kim, et al.
Clinical Genetics
|
March 23, 2021
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features
Junwon Lee, Hyunjoo Lee, Young-Mock Lee, et al.
International Journal of Molecular Sciences
|
January 21, 2023
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model
Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, et al.
JAMA Ophthalmology
|
November 18, 2017
Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome
John Hoon Rim, Seung-Tae Lee, Heon Yung Gee, et al.
Molecular Vision
|
March 14, 2020
Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis
Dongheon Surl, Saeam Shin, Seung-Tae Lee, et al.
Molecular Vision
|
April 11, 2024
Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of <i>PRDM13</i> causing North Carolina macular dystrophy in Korea
Yuri Seo, Kwangsic Joo, Junwon Lee, et al.
Research Square
|
June 5, 2025
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration
Riccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Translational Vision Science & Technology
|
June 28, 2022
Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus
Junwon Lee, Han Jeong, Dongju Won, et al.
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of 11
Search research articles
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Showing results (71-80 of 102) with videos related to
Sort By:
Page
of 11
Korean Journal of Ophthalmology : KJO
|
June 30, 2025
Therapeutic Effect of Topical 0.125% Atropine in South Korean Myopic Children: A Real-World Experience
Dae Hee Kim, Jinu Han, Kyung-Ah Park, et al.
Scientific Reports
|
October 14, 2024
Proteomic analysis of CD29+ Müller cells reveals metabolic reprogramming in rabbit myopia model
Chae-Eun Moon, Jun-Ki Lee, Hyunjin Kim, et al.
Epidemiologia (Basel, Switzerland)
|
November 24, 2025
Clinical Features According to the Type of Intermittent Exotropia: Korean Intermittent Exotropia Multicenter Study
Hee Kyung Yang, Hae Ri Yum, Sun A Kim, et al.
Clinical Genetics
|
March 23, 2021
DYNC2H1 variants cause Leber congenital amaurosis without syndromic features
Junwon Lee, Hyunjoo Lee, Young-Mock Lee, et al.
International Journal of Molecular Sciences
|
January 21, 2023
Retinal Proteome Analysis Reveals a Region-Specific Change in the Rabbit Myopia Model
Chae-Eun Moon, Yong Woo Ji, Jun-Ki Lee, et al.
JAMA Ophthalmology
|
November 18, 2017
Accuracy of Next-Generation Sequencing for Molecular Diagnosis in Patients With Infantile Nystagmus Syndrome
John Hoon Rim, Seung-Tae Lee, Heon Yung Gee, et al.
Molecular Vision
|
March 14, 2020
Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis
Dongheon Surl, Saeam Shin, Seung-Tae Lee, et al.
Molecular Vision
|
April 11, 2024
Two novel non-coding single nucleotide variants in the DNase1 hypersensitivity site of <i>PRDM13</i> causing North Carolina macular dystrophy in Korea
Yuri Seo, Kwangsic Joo, Junwon Lee, et al.
Research Square
|
June 5, 2025
Variants in the ciliopathy gene SCLT1 are associated with non-syndromic retinal degeneration
Riccardo Sangermano, Kaoru Fujinami, Suk Ho Byeon, et al.
Translational Vision Science & Technology
|
June 28, 2022
Noncanonical Splice Site and Deep Intronic FRMD7 Variants Activate Cryptic Exons in X-linked Infantile Nystagmus
Junwon Lee, Han Jeong, Dongju Won, et al.
Page
of 11