Resultados de procura - Joo, Kwangsic

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

Ligazón do recurso Ligazón do recurso Ligazón do recurso

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

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Clinical Characterization of Korean Patients with Pseudoxanthoma Elasticum and Angioid Streaks por 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? por 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 por 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 por 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 por 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 por 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 por 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 por 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 por 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 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

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CCDC41 is required for ciliary vesicle docking to the mother centriole por 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 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

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