Search Results - Joo, Kwangsic

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  1. 1
    Pigmented Paravenous Retinochoroidal Atrophy

    Pigmented Paravenous Retinochoroidal Atrophy by Choi, Won Jong, Joo, Kwangsic, Park, Kyu Hyung

    Published 2020
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  2. 2
    Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review

    Ophthalmic Manifestations and Genetics of the Polyglutamine Autosomal Dominant Spinocerebellar Ataxias: A Review by Park, Jun Young, Joo, Kwangsic, Woo, Se Joon

    Published 2020
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  3. 3
    Clinical Characterization of Korean Patients with Pseudoxanthoma Elasticum and Angioid Streaks

    Clinical Characterization of Korean Patients with Pseudoxanthoma Elasticum and Angioid Streaks by Jin, Ki Won, Joo, Kwangsic, Woo, Se Joon

    Published 2021
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  4. 4
    Author Response: Does the Fc Region Have a Role in the Ocular Half-Life After Intravitreal Injection?

    Author Response: Does the Fc Region Have a Role in the Ocular Half-Life After Intravitreal Injection? by Joo, Kwangsic, Choi, Yewon, Chung, Jae-Yong, Woo, Se Joon

    Published 2020
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  5. 5
    Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients

    Clinical and Genetic Characteristics of Korean Congenital Stationary Night Blindness Patients by Kim, Hyeong-Min, Joo, Kwangsic, Han, Jinu, Woo, Se-Joon

    Published 2021
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  6. 6
    Angiogenin ameliorates corneal opacity and neovascularization via regulating immune response in corneal fibroblasts

    Angiogenin ameliorates corneal opacity and neovascularization via regulating immune response in corneal fibroblasts by Lee, Seung Hoon, Kim, Kyoung Woo, Joo, Kwangsic, Kim, Jae Chan

    Published 2016
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  7. 7
    Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans

    Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans by Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Published 2019
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  8. 8
    Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient

    Congenital Stationary Night Blindness due to Novel TRPM1 Gene Mutations in a Korean Patient by Lee, Yun Jeong, Joo, Kwangsic, Seong, Moon-Woo, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Published 2020
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  9. 9
    Efficacy of bevacizumab for vitreous haemorrhage in proliferative diabetic retinopathy with prior complete panretinal photocoagulation

    Efficacy of bevacizumab for vitreous haemorrhage in proliferative diabetic retinopathy with prior complete panretinal photocoagulation by Park, Young Joo, Ahn, Jeeyun, Kim, Tae Wan, Park, Sang Jun, Joo, Kwangsic, Park, Kyu Hyung, Shin, Joo Young

    Published 2021
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  10. 10
    Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

    Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases by Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Published 2019
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  11. 11
    Erratum: Correction of Table: Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases

    Erratum: Correction of Table: Genetic Mutation Profiles in Korean Patients with Inherited Retinal Diseases by Kim, Min Seok, Joo, Kwangsic, Seong, Moon-Woo, Kim, Man Jin, Park, Kyu Hyung, Park, Sung Sup, Woo, Se Joon

    Published 2019
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  12. 12
    Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation

    Severe or Profound Sensorineural Hearing Loss Caused by Novel USH2A Variants in Korea: Potential Genotype-Phenotype Correlation by Lee, Sang-Yeon, Joo, Kwangsic, Oh, Jayoung, Han, Jin Hee, Park, Hye-Rim, Lee, Seungmin, Oh, Doo-Yi, Woo, Se Joon, Choi, Byung Yoon

    Published 2020
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  13. 13
    CCDC41 is required for ciliary vesicle docking to the mother centriole

    CCDC41 is required for ciliary vesicle docking to the mother centriole by Joo, Kwangsic, Kim, Chang Gun, Lee, Mi-Sun, Moon, Hyun-Yi, Lee, Sang-Hee, Kim, Mi Jeong, Kweon, Hee-Seok, Park, Woong-Yang, Kim, Cheol-Hee, Gleeson, Joseph G., Kim, Joon

    Published 2013
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  14. 14
    Genetic Characteristics and Phenotype of Korean Patients with Stickler Syndrome: A Korean Multicenter Analysis Report No. 1

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

    Published 2021
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  15. 15
    Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3

    Visual Field Characteristics in East Asian Patients With Occult Macular Dystrophy (Miyake Disease): EAOMD Report No. 3 by Ahn, Seong Joon, Yang, Lizhu, Tsunoda, Kazushige, Kondo, Mineo, Fujinami-Yokokawa, Yu, Nakamura, Natsuko, Iwata, Takeshi, Kim, Min Seok, Mun, Yongseok, Park, Jun Young, Joo, Kwangsic, Park, Kyu Hyung, Miyake, Yozo, Sui, Ruifang, Fujinami, Kaoru, Woo, Se Joon

    Published 2022
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  16. 16
    Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability

    Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability by Failler, Marion, Gee, Heon Yung, Krug, Pauline, Joo, Kwangsic, Halbritter, Jan, Belkacem, Lilya, Filhol, Emilie, Porath, Jonathan D., Braun, Daniela A., Schueler, Markus, Frigo, Amandine, Alibeu, Olivier, Masson, Cécile, Brochard, Karine, Hurault de Ligny, Bruno, Novo, Robert, Pietrement, Christine, Kayserili, Hulya, Salomon, Rémi, Gubler, Marie-Claire, Otto, Edgar A., Antignac, Corinne, Kim, Joon, Benmerah, Alexandre, Hildebrandt, Friedhelm, Saunier, Sophie

    Published 2014
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