Pigmented Paravenous Retinochoroidal Atrophy

por Choi, Won Jong, Joo, Kwangsic, Park, Kyu Hyung
Publicado 2020

Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review

por Park, Jun Young, Joo, Kwangsic, Woo, Se Joon
Publicado 2020

Clinical Characterization of Korean Patients with Pseudoxanthoma Elasticum and Angioid Streaks

por Jin, Ki Won, Joo, Kwangsic, Woo, Se Joon
Publicado 2021

Author Response: Does the Fc Region Have a Role in the Ocular Half-Life After Intravitreal Injection?

por Joo, Kwangsic, Choi, Yewon, Chung, Jae-Yong, Woo, Se Joon
Publicado 2020

Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients

por Kim, Hyeong-Min, Joo, Kwangsic, Han, Jinu, Woo, Se-Joon
Publicado 2021

Angiogenin ameliorates corneal opacity and neovascularization via regulating immune response in corneal fibroblasts

por Lee, Seung Hoon, Kim, Kyoung Woo, Joo, Kwangsic, Kim, Jae Chan
Publicado 2016

Discontinuation of treatment and retreatment of neovascular age-related macular degeneration in the real-world: Bundang AMD cohort study report 5

por Cho, Soo Chang, Park, Kyu Hyung, Park, Sang Jun, Joo, Kwangsic, Woo, Se Joon
Publicado 2023

Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans

por Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2019

Clinical and Genetic Characteristics of Retinal Capillary Hemangioblastoma in Korean Patients

por Lee, Sang Ha, Park, Kyu Hyung, Woo, Se Joon, Park, Sang Jun, Joo, Kwangsic
Publicado 2022

Clinical and Genetic Features of Korean Patients with Achromatopsia

por Choi, Yong Je, Joo, Kwangsic, Lim, Hyun Taek, Kim, Sung Soo, Han, Jinu, Woo, Se Joon
Publicado 2023

Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

por Lee, Yun Jeong, Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2020

Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

por Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2019

Erratum: Correction of Table: Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

por Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon
Publicado 2019

Proteomic genotyping of SNP of Complement Factor H (CFH) Y402H and I62V using multiple reaction monitoring (MRM) assays

por Kim, Kyoung Lae, Kim, Hyerim, Lee, Youngju, Lee, Cheolju, Joo, Kwangsic, Park, Sang Jun, Park, Kyu Hyung, Park, Seong-Jun, Woo, Se Joon
Publicado 2022

Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation

por Lee, Sang-Yeon, Joo, Kwangsic, Oh, Jayoung, Han, Jin Hee, Park, Hye-Rim, Lee, Seungmin, Oh, Doo-Yi, Woo, Se Joon, Choi, Byung Yoon
Publicado 2020

Voretigene Neparvovec for the Treatment of RPE65-associated Retinal Dystrophy: Consensus and Recommendations from the Korea RPE65-IRD Consensus Paper Committee

por Han, Jinu, Joo, Kwangsic, Kim, Ungsoo Samuel, Woo, Se Joon, Lee, Eun Kyoung, Lee, Joo Yong, Park, Tae Kwann, Kim, Sang Jin, Byeon, Suk Ho
Publicado 2023

Genotypic Profile and Clinical Characteristics of CRX-Associated Retinopathy in Koreans

por Kim, Dong Geun, Joo, Kwangsic, Han, Jinu, Choi, Mihyun, Kim, Seong-Woo, Park, Kyu Hyung, Park, Sang Jun, Lee, Christopher Seungkyu, Byeon, Suk Ho, Woo, Se Joon
Publicado 2023

Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1

por Choi, Soon-Il, Woo, Se-Joon, Oh, Baek-Lok, Han, Jinu, Lim, Hyun-Taek, Lee, Byung-Joo, Joo, Kwangsic, Park, Jun-Young, Jang, Ja-Hyun, So, Min-Kyung, Kim, Sang-Jin
Publicado 2021

Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No...

por Fujinami-Yokokawa, Yu, Yang, Lizhu, Joo, Kwangsic, Tsunoda, Kazushige, Liu, Xiao, Kondo, Mineo, Ahn, Seong Joon, Li, Hui, Park, Kyu Hyung, Tachimori, Hisateru, Miyata, Hiroaki, Woo, Se Joon, Sui, Ruifang, Fujinami, Kaoru
Publicado 2023

Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin

por Jung, Young Hoon, Kwak, Jay Jiyong, Joo, Kwangsic, Lee, Hyuk Jun, Park, Kyu Hyung, Kim, Min Seok, Lee, Eun Kyoung, Byeon, Suk Ho, Lee, Christopher Seungkyu, Han, Jinu, Lee, Junwon, Yoon, Chang Ki, Woo, Se Joon
Publicado 2023