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Frontiers in Genetics
|
September 15, 2023
Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin
Young Hoon Jung, Jay Jiyong Kwak, Kwangsic Joo, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
JAMA Network Open
|
May 31, 2024
Clinician-Driven Reanalysis of Exome Sequencing Data From Patients With Inherited Retinal Diseases
Dongheon Surl, Dongju Won, Seung-Tae Lee, et al.
Research Square
|
February 26, 2024
Coding and non-coding variants in the ciliopathy gene <i>CFAP410</i> cause early-onset non-syndromic retinal degeneration
Riccardo Sangermano, Priya Gupta, Cherrell Price, et al.
NPJ Genomic Medicine
|
November 8, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration
Riccardo Sangermano, Priya Gupta, Cherrell Price, et al.
Korean Journal of Ophthalmology : KJO
|
February 3, 2026
Myopia Management Consensus Statement in Korean Children 2025 by the Korean Myopia Society for KAPOS
Yeon-Hee Lee, Jae Yun Sung, Sun Young Shin, et al.
American Journal of Ophthalmology
|
March 8, 2025
Retinitis Pigmentosa GTPase Regulator-Associated X-Linked Retinitis Pigmentosa: Molecular Genetics and Clinical Characteristics
Sungsoon Hwang, Sohee Jeon, Je Moon Yoon, et al.
Ophthalmology. Retina
|
February 26, 2021
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients
Yusuke Murakami, Yoshito Koyanagi, Masatoshi Fukushima, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 28, 2024
Prognostic factors of first-onset optic neuritis based on diagnostic criteria and antibody status: a multicentre analysis of 427 eyes
Young Gi Min, Yeji Moon, Young Nam Kwon, et al.
Ophthalmology
|
February 14, 2022
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study
Helen J Kuht, Gail D E Maconachie, Jinu Han, et al.
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Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Frontiers in Genetics
|
September 15, 2023
Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin
Young Hoon Jung, Jay Jiyong Kwak, Kwangsic Joo, et al.
Human Molecular Genetics
|
August 4, 2020
SLC38A8 mutations result in arrested retinal development with loss of cone photoreceptor specialization
Helen J Kuht, Jinu Han, Gail D E Maconachie, et al.
JAMA Network Open
|
May 31, 2024
Clinician-Driven Reanalysis of Exome Sequencing Data From Patients With Inherited Retinal Diseases
Dongheon Surl, Dongju Won, Seung-Tae Lee, et al.
Research Square
|
February 26, 2024
Coding and non-coding variants in the ciliopathy gene <i>CFAP410</i> cause early-onset non-syndromic retinal degeneration
Riccardo Sangermano, Priya Gupta, Cherrell Price, et al.
NPJ Genomic Medicine
|
November 8, 2024
Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration
Riccardo Sangermano, Priya Gupta, Cherrell Price, et al.
Korean Journal of Ophthalmology : KJO
|
February 3, 2026
Myopia Management Consensus Statement in Korean Children 2025 by the Korean Myopia Society for KAPOS
Yeon-Hee Lee, Jae Yun Sung, Sun Young Shin, et al.
American Journal of Ophthalmology
|
March 8, 2025
Retinitis Pigmentosa GTPase Regulator-Associated X-Linked Retinitis Pigmentosa: Molecular Genetics and Clinical Characteristics
Sungsoon Hwang, Sohee Jeon, Je Moon Yoon, et al.
Ophthalmology. Retina
|
February 26, 2021
Genotype and Long-term Clinical Course of Bietti Crystalline Dystrophy in Korean and Japanese Patients
Yusuke Murakami, Yoshito Koyanagi, Masatoshi Fukushima, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 28, 2024
Prognostic factors of first-onset optic neuritis based on diagnostic criteria and antibody status: a multicentre analysis of 427 eyes
Young Gi Min, Yeji Moon, Young Nam Kwon, et al.
Ophthalmology
|
February 14, 2022
Genotypic and Phenotypic Spectrum of Foveal Hypoplasia: A Multicenter Study
Helen J Kuht, Gail D E Maconachie, Jinu Han, et al.
Page
of 11