Torthaí cuardaigh - Joo, Kwangsic

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

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

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

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

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

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

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

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

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

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

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

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

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CCDC41 is required for ciliary vesicle docking to the mother centriole de réir 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

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

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

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Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability de réir 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

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